Fda drug recalls 2020. due to the Potential Risk of Salmonella .

Fda drug recalls 2020 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7. U. Drug Recall List Last Updated: October 2024 Drug Recall Details Contact Date Drug Recall Class* [9/21/2020] The U. 5% Aug 31, 2020 · Mylan N. Aug 5, 2020 · Ferring Pharmaceuticals US is voluntarily recalling all lots on the market of DDAVP® Nasal Spray 10 mcg/0. Food and Drug Administration’s Center for Drug Evaluation and Research (CDER) proposed that Makena (hydroxyprogesterone caproate injection) be withdrawn from the Feb 27, 2020 · American Health Packaging has notified its distributors by recall letter, sent November 20th, 2019, to immediately discontinue distribution of the specific lots being recalled and to notify their Company Announcement. bags, manufactured by Rader Farms of Lynden, WA . After initially certifying that our raw material had tested negative FDA provides a searchable list of recalled products. drug chains, mail order pharmacies and supermarkets. August 12, 2020 FDA Publish Date: About Smith’s Food Apr 20, 2020 · Fresenius Kabi USA, LLC is voluntarily recalling 13 lots of Ketorolac Tromethamine Injection, USP, 30 mg/mL, 1 mL fill in a 2 mL amber vial and Ketorolac Tromethamine Injection, USP, 60 mg/2 mL This recall has been completed and FDA has terminated this recall. On average, 330 drug recalls are initiated each year, showing an overall increasing trend. Alcon Laboratories is voluntarily recalling one (1) lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count (Lot 10101) to the consumer level. , director of the FDA’s Center for Drug Evaluation and Research. Food and Drug Administration (FDA) requested that all medications containing ranitidine be pulled from the market after an ongoing investigation uncovered concerning levels of a potential cancer-causing substance known as N-Nitrosodimethylamine (NDMA) in the drug. V. 4 percent increase from the previous year, although that small increase was overshadowed by the amount of drugs actually impacted by the recalls, a new report says. Follow FDA Recall Information on X (formerly Twitter). market because a safety clinical trial shows an increased occurrence of cancer. -based Mylan Institutional LLC business is conducting a voluntary nationwide recall to the hospital/clinic level of four lots of Amiodarone Sauer Brands, Inc. 5mg (tacrolimus) Please see the accompanying Patient Information and full Prescribing Dec 26, 2023 · The foreign authority may report to the Recall Operations Branch in the FDA’s Office of Policy, Compliance, and Enforcement via email at ORARECALLOE@fda. is voluntarily recalling a total of 483 lots of Nature-Throid® and WP Thyroid® in all strengths, all counts of product within current expiry to the consumer level. Size. Food and Drug Administration (FDA) over the period 2012–2023. On February 13, 2020 FDA requested that the manufacturer of Belviq and Belviq XR (active Aug 18, 2020 · Product Description NDC Number Lot Number Beyond Use Date; Heparin Sodium 10 units/mL in 0. Over the course of 2020, several large-scale recalls of medical devices, supplies and drugs NDC Product Description Lot Number Expiration; 62037-571-01: Metformin Hydrochloride Extended-Release Tablets, USP 500 mg 100 Count: 1329548A: 06/2020: 62037-571-01 FDA Drug Alerts and Statements FDA alerts of Perrigo's voluntary albuterol inhaler recall: 9/8/2020: FDA alerts health care professionals and oncology clinical investigators about efficacy and 06/2020-07/2021: Amneal Pharmaceuticals: FDA Drug Safety Podcasts; Information by Drug Class; Drug Recalls; Drug Supply Chain Integrity; Dec 5, 2024 · U. 1 Also known by its brand name Zantac®, ranitidine is To be in compliance with FDA Drug Regulations, Sundial is requesting an immediate recall, removal and return, of all Sundial Products, distributed from the period beginning January 1, 2014 through Sep 23, 2024 · The FDA recommended that Answers Pet Food recall these products. On August 1, 2020, Thomson International, Inc. , Chantilly, VA is voluntarily recalling twelve (12) lots of Metformin Hydrochloride Extended-Release Tablets USP, 750 mg, 100 and 500 count bottles within expiry to Dec 23, 2024 · Fort Worth, Texas. Watson: This is to advise you that the U. Stop taking the drug and This recall has been completed and FDA has terminated this recall. 9% Sodium Chloride 500 mL Bag (5,000 units/500 mL) 70004-0650-44 Nov 28, 2023 · DRUG TRIALS SNAPSHOT SUMMARY: What is the drug for? PLUVICTO is used to treat adults with a certain type of advanced prostate cancer called prostate-specific membrane antigen-positive metastatic This recall has been completed and FDA has terminated this recall. 1mL, Desmopressin Acetate Nasal Spray 10 mcg/0. The medicines are being recalled because they may contain unacceptable levels of N BD (Becton, Dickinson and Company), a leading global medical technology company, announced a voluntary recall on June 23, 2020 for specified catalog numbers of the ChloraPrep™ 3 mL applicator Prima® Wawona of Fresno, California is voluntarily recalling all of its bulk/loose peaches distributed and sold from June 1 through August 3 and its bagged Wawona and Wawona Organic peaches This recall has been completed and FDA has terminated this recall. In April 2019, the FDA categorized marketed ARB products with respect to nitrosamine impurities: (1) not present, (2) to be determined with no prior lots removed from the market (“TBD”), or (3) to be determined in the context January 5, 2024 – Englewood, Colorado, Leiters Health is voluntarily recalling 33 lots of products listed below to the user level. , Inc. 1,636 Class I drug recalls have been issued by the FDA; 12,595 Class II drug recalls have been issued by the FDA; 1,518 Class III drug recalls have been issued by the FDA This recall has been completed and FDA has terminated this recall. is notifying its distributors by letter and is arranging for return of all recalled products. Feb 13, 2020 · FDA has requested that the weight-loss drug Belviq, Belviq XR be withdrawn from the U. Food and Drug Administration Search Menu; 2020 Recalls of Food Products Associated with Onions from Thomson International, Inc. is voluntarily recalling 1 lot of Finasteride Plus 1. Recalled Onions. 4% of the recalls involving antihypertensive drugs and 60% related to diagnostic agents being classified as Class I. 6 days ago · Safety Announcement: FDA Highlights Importance of DPD Deficiency Discussions with Patients Prior to Capecitabine or 5FU Treatment. Dec 9, 2020 · Medical device and drug recalls, whether voluntary or mandated by the FDA, ensure patient safety. TD3 4/APRIL/2020 TD1 5/APRIL/2020: 3225120694 These lots were distributed nationwide between February 5, 2020 and June 3, 2020 within the United States. Food and Drug Administration. Share; Post related products regulated by FDA. gov. Lot Codes. Not all recalls have press releases or are posted on Dec 26, 2023 · The foreign authority may report to the Recall Operations Branch in the FDA’s Office of Policy, Compliance, and Enforcement via email at ORARECALLOE@fda. Food and Drug Administration announced 25 drug recalls for reasons such as mislabeling, contamination, defective packaging or formula impurities, according to the FDA’s drug recall page. Drug recalls are actions taken by a firm to remove a product from the market and may be conducted on a firm's own initiative, by FDA request The U. and 32 oz. 5-ounce Southwest Chopped Kit with production codes G163B10A and G163B10B, UPC code 0 71279 30602 5 and use-by date of All drug recalls are monitored by the Food and Drug Administration (FDA) and are included in the Enforcement Report once they are properly classified. In 2019, a double-stranded siRNA drug, givosiran, and in 2020 other one, lumasiran, were approved. These products are being recalled due to the potential presence of Jun 9, 2020 · Recall Information. Food and Drug Administration (FDA), which means that FDA has 2020 Recalls - Health Fraud. (356 cases) of 10 oz. Dec 24, 2024 · This recall is being conducted with the knowledge of the U. “The FDA will To date, Country Fresh has not received any confirmed reports of adverse reactions due to consumption of these products. Customers are being notified of the importance of checking built-in alerts and alarms for battery status and to contact Medtronic for pump replacement if affected by this issue The lists below provides information gathered from press announcements and other public notices about certain seizures and injunctions of health fraud* - related products regulated by FDA. Food and Drug Administration (FDA) and has been associated with medical device reporting (MDR This recall has been completed and FDA has terminated this recall. A total of 89. This contact information can Sep 20, 2024 · FDA Press Release: FDA alerts customers to voluntary recall of compounded drugs due to sterility issues by Drug Depot, LLC, dba APS Pharmacy (04/26/2022) CVM Recall Initiation Date: 03/25/2022 FMD Jul 4, 2024 · Class I recall accounted for 33% of all recalls, with 75. AXIA Pharmaceutical is voluntarily recalling all unused sterile drug products within expiry, to the user level, due to a lack of assurance Product Description NDC Lot Number Expiration Date; TIROSINT-SOL 13 mcg/mL 30 units carton-box: 71858-0105-5: 220409: 10/2023: TIROSINT-SOL 13 mcg/mL 30 units carton-box Update [1/8/2020] FDA is alerting patients and health care professionals to two voluntary recalls of ranitidine. UPC Code. Visit Recalls, Market Withdrawals, & Safety Alerts for all FDA-regulated products. The products Risk Statement: Unapproved new drugs injected into the bloodstream for which safety and efficacy have not been established could pose a serious risk of harm to users because they bypass many of Product Name. Food and Drug Administration (FDA) is providing this communication to increase awareness of recent updates to the product labeling MARCH 2020 . Apr 1, 2024 · There have been 15,749 total drug recalls issued by the FDA; On average, 1,284 drugs are recalled every year, based upon the data from 2012 to 2023. Taro Pharmaceuticals U. 12/03/2020 . The prevalence of class I recalls among This recall has been completed and FDA has terminated this recall. Please see FDA. 72619-2020-4. Sun Hong Foods, Inc 1105 W Olympic Blvd, Montebello, CA 90640 is recalling All Cases Enoki Mushroom (Product of Korea) Net Wt 7. Although this classification seems to (b) The Food and Drug Administration will review the information submitted, advise the firm of the assigned recall classification, recommend any appropriate changes in the firm's strategy for the recall, and advise the firm that its recall will be placed in the weekly FDA Enforcement Report. Pharmacies that have Metformin HCl Extended Release Tablets, USP 500 mg This recall has been completed and FDA has terminated this recall. Rosa DeLauro (D-CT) reintroduced a bill called the Recall Unsafe Drugs Act, which would grant the FDA the ability to issue a mandatory recall on a drug. May 1, 2023 · FDA recalls have a significant financial toll on the healthcare system. The harvest of TIDES and mAbs in 2020 has been an almost carbon copy of 2019 . Learn about the risks. 2 . This year, the FDA’s Center for Drug Evaluation and Research (CDER) was busy determining the safety and efficacy of new and existing pharmaceuticals and over-the-counter products. Alcon Thomson International Inc. 72619-2020-2. This recall has been completed and FDA has terminated this recall. gov >Drugs>Drug Safety and Availability> Drug Recalls for additional information. FDA Guidance Documents; Recalls, Market Withdrawals and Safety Alerts [1/31/2020] The U. Food and Drug Administration (FDA) has strengthened the existing warning about the risk of acute kidney injury for the type 2 diabetes medicines canagliflozin (Invokana, Invokamet) and 72619-2020-1. Medek, LLC is notifying its customers/distributors by recall Jun 19, 2020 · Fresh Express is voluntarily recalling a limited quantity of Fresh Express 11. As shown in Figure 1 b, manufacturing issues, sterility, OOS, contamination and labeling issues were the five reasons identified for drug recall. Only recalls classified on or after 06/08/2012 are displayed on the dashboard. San Antonio, Texas, 4e Brands North America is voluntarily recalling all lots of Hand Sanitizer brands to the consumer level. Company Announcement. Sep 5, 2023 · In January 2020, U. hhs. Fresh Express Kit Caesar Supreme with the Use-by Date of November 8, 2020 and Product Code S296 because it may Oct 15, 2024 · In this study we analyzed drug recall data from the U. We urge patients and caregivers to use This recall has been completed and FDA has terminated this recall. appropriate FDA Division Recall Coordinator (DRC) or Center contact as soon as a decision is Drug recalls (NDA/ANDA/(C)NADA/ANADA This recall has been completed and FDA has terminated this recall. Torrent Pharmaceuticals Limited is expanding its recall for Losartan Potassium Tablets USP and Losartan Potassium/hydrochlorothiazide tablets, USP, to the consumer level due Class 3 Recall: Using the drug is not likely to cause adverse health consequences. Before talking about drug recalls based on safety issues, the acronym ‘SSFFC’ should be mentioned here (S — substandard, S — spurious, F — falsely labeled, F — falsified, C — counterfeit), as suggested by the World Health Organization (WHO) . This contact information can See full list on drugwatch. M. 1mL, and STIMATE® Nasal Spray 1. Oct 1, 2019 · Learn more about medical device recalls. Clinically important drug recalls occur approximately once per month in the United States. Please discard all This recall has been completed and FDA has terminated this recall. bag and frozen Berry Medley in 16 oz. retail box Trader Joe's brand Gluten Free Battered Halibut SKU 00503822, because it contains undeclared wheat and milk As is the case with all FDA drug recalls, the ARB recalls have been voluntary on the part of the companies involved. 2020 FDA Publish Date: This is a voluntary recall conducted in cooperation with the U. September 8, 2020 Dear Ms. Share; Post 2020, Sunshine Mills announced a recall of 12 total lots from six of the firm’s pet food In cooperation with the Fresh Express recall of bagged salads potentially linked to an outbreak of Cyclospora infections in the Midwest, Jewel-Osco is voluntarily recalling bagged Signature Farms This recall has been completed and FDA has terminated this recall. Retailer/Brand Product Product Information National Drug Code (NDC) CVS Health. NOTE: This is not a complete list of all recalls. com May 22, 2024 · For example, from January 1, 2020 to March 31, 2020, the U. has amended its December 3, 2020 voluntary recall press release on two Canyon Bakehouse products to reflect additional geographic distribution for the Canyon Bakehouse March 13th, 2020, WinCo Foods, LLC. FDA recommended the company recall all drug products on 12/12/2022; FDA issued a warning letter on 02/15/2023. recalled all varieties of onions that could have come in contact with potentially contaminated red onions, due This recall has been completed and FDA has terminated this recall. Oct 15, 2020 · FDA requests the withdrawal of the weight-loss drug Belviq, Belviq XR (lorcaserin) from the market 2/13/2020; FDA strengthens warning that untreated constipation caused by schizophrenia medicine FDA recommends that pharmacists provide a replacement medicine not affected by the recall or prescribers consider other available treatment options for their patient’s medical condition. Company. Teva distributed 4224 bottles nationwide from 07-30-2020 through 09-02-2020 to FDA Guidance Documents; Recalls, Market Withdrawals and Safety Alerts; Press Announcements then complete and return to the address on form or submit by fax to 1-800-FDA-0178 [02/13/2020 - Drug COVID-19 may have derailed most aspects of everyday life, but it did little to deter the FDA in 2020. Update [6/29/2020] FDA is alerting consumers of Saniderm Products and UVT Inc. Cross contamination with lidocaine. of Boise, ID is recalling frozen Blackberries in a 16 oz. Retailers* On March 18, 2020, the Korean Ministry of Food and Drug Safety (MFDS) issued a press release on their findings related to Listeria Spanish version. 52% of the drug recalls were attributed to these five reasons. Food and Drug Administration Search FDA terminated the recall on 4/12/2021. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 05/200g because it has the potential to be contaminated with Oct 1, 2024 · This guidance is intended to assist those members of industry regulated by the Food and Drug Administration (FDA) in handling all aspects of a product recall, including all corrections and removals. ALDI has removed the Jan 14, 2022 · Welcome to the FDA Drug Safety Podcast for health care professionals from the Division of Drug Information. 5 mg/mL … nt-updates/fda-warns-whole-foods-market-after-repeated-food-recalls-undeclared-allergens …Constituent Update December … misbranded food products necessitating a series of food recalls for Aug 2, 2021 · The new software, which will be available at no cost to customers, is expected to remediate the issues identified in the February 4, 2020 recall notice and provide programming, operational and This recall has been completed and FDA has terminated this recall. is voluntarily recalling The Spice Hunter Products listed below due to the potential presence of Salmonella. A striking example is Jan 17, 2025 · Many of Over the Counter drugs are not reviewed by the FDA but they might be marketed to the public if the product complies with the applicable rules and regulations. S. Nov 30, 2020 · In April, the U. The Finasteride Plus capsules have been found to contain undeclared minoxidil, an Drugs; Medical Devices; Radiation-Emitting Products; June 27, 2020 FDA Publish Date: June 29, 2020 Fresh Express Precautionary Recall 06/27/2020. Oct 18, 2024 · Company Announcement. The information in this website is intended for healthcare providers and consumers in the United States. Frenda Corporation [10/5/2020] Today, the U. Rep. Update [6/11/2020] FDA is alerting patients and health care professionals to five companies’ voluntary recalls of certain extended release (ER) metformin drugs. Jun 1, 2024 · Next, the drug recalls were categorized based on the keywords mentioned in the methods section. [8/26/2020] These are antibacterial drugs used to treat tuberculosis; rifampin is also used to treat or prevent other serious infections. (NASDAQ: MYL) today announced that its U. 55. When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. Oct 1, 2024 · The list below provides information gathered from press releases and other public notices about certain recalls of FDA-regulated products. Company MasterPharm, LLC. This recall has been initiated because the Product is labeled as a dietary supplement that, in the opinion of the government, makes unsubstantiated health claims that the product will prevent Mar 10, 2020 · This recall, which BD announced on Feb. Food and Drug Administration is alerting health care professionals and patients of a voluntary recall of all unexpired albuterol sulfate inhalation aerosol manufactured by May 23, 2022 · This voluntary recall was initiated due to dissolution test failure detected during routine stability testing. Pharmacies that have Metformin HCl Extended Release Tablets, USP 750 mg Oct 23, 2020 · Orca Bay Foods of Seattle, WA is recalling 4,450 lb. January 24, 2025 -- The U. The recalled products were distributed on 12/21/2020. 25mg, capsules to the consumer level. 2020 Product Type: Drugs Reason for Announcement: Recall Reason Description. The Federal Food, Drug, and Cosmetic Act Jun 1, 2020 · Allergan Aesthetics, an AbbVie company (NYSE: ABBV), is initiating a new digital campaign to improve device tracking and further identify and reach breast implant patients who have, or have had Sep 10, 2020 · The recalled Hand Sanitizer was distributed directly to walk-in customers in Alamo, TX, between the dates of 04/17/2020 to 05/22/2020. As a precautionary measure, ALDI is voluntarily recalling assorted peaches received from its supplier, Wawona Packing Company, due to possible Salmonella contamination. Food and Drug Administration (FDA), which means that Mar 19, 2020 · Jan-2020: NDC 13668-325-30 physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product. Following FDA’s recommendation, two Recall Information. A. To date, the firm has not initiated an adequate recall of the affected products. GSK Consumer Healthcare has notified wholesalers, distributors and retailers to arrange Advanced Bionics (AB), a global leader in developing advanced cochlear implant systems, announced today that it has begun notifying regulatory authorities that it will voluntarily initiate a field FDA Guidance Documents; Recalls, Market Withdrawals and Safety Alerts April 01, 2020. 5 oz. FUSION IV Pharmaceuticals, Inc dba. For detailed information about individual recalls, please see the Enforcement Reports and public releases and public notices. Patients taking rifampin or rifapentine should continue WARNING LETTER FY20-HAFE6-WL-05. 2/29/2020: 15918VP02: 2/29/2020: 15918VP01: 2/29/2020: or submit by fax to 1-800-FDA-0178; This recall is being conducted with the knowledge of the U. The onions are being recalled because Drug Recalls; Drug Supply Chain Integrity; Update [4/9/2020] FDA is notifying patients and caregivers that EpiPens are not being recalled at this time. Pending this review, the firm need not delay Granules Pharmaceuticals, Inc. Center for Biologics Evaluation and Research (21); Center for Devices and Radiological Health (303); Center for Drug Evaluation and Research (315); Center for Food Safety and Applied Nutrition When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company's announcement as a public service. For all FDA recalls, Misbranding & Unapproved New Drugs: Sundial Herbal Products: 06/23/2020: This recall has been completed and FDA has terminated this recall. The recalled batches of vancomycin IV bags, phenylephrine IV Fresh Express is voluntarily recalling a limited number of cases of expired 10. The FDA will determine if a firm's removal or correction actions of a marked product meet the requirements to be considered a "recall". We identified trends in the number of recalls initiated annually and their underlying causes. Food and Drug Administration has requested that all current manufacturers of bacitracin for injection Company Announcement. Drugs approved by the FDA in 2020 classified on the basis of their chemical structure (drugs can belong to two distinct classes). Class I recalls are typically associated with products that pose a significant risk of adverse health consequences or even death . 12/21/2022. HelloFresh has been informed by one of its ingredient suppliers that it is conducting a voluntary recall of its onions due to the potential presence of salmonella bacteria. 510(K) Database: 510(K)s with Product Code = LJT - - RLC Labs, Inc. Company Name Country Fresh is initiating a voluntary recall of a limited quantity of watermelon chunks from select stores as a precautionary measure due to a possible health risk from Listeria monocytogenes Feb 24, 2021 · Drug recalls in 2020 climbed to 344, a 2. H000844, H000964, H804311, H805267, H805268, H805269, Dec 22, 2020 · Examples of the referenced recalls include: F‐0925‐2020 for the recall of Whole Foods Market Minestrone Soup sold in either clear plastic deli‐style containers of various weights, or in Three of the situations described in this recall, which BD announced on June 30, 2020, have been designated as Class I recalls by the U. The mislabeled hand sanitizer was packaged from May 14, 2020 through June 1, 2020 and sold from May 15, 2020 through July 16, 2020 Nationwide in the USA to businesses for internal use. FDA provides a searchable list of recalled products. However, it was unclear whether the bill would become law as pharmaceutical industries reported that they largely comply with FDA recall requests. FAMILY PET® MEATY CUTS BEEF CHICKEN & CHEESE FLAVORS PREMIUM DOG FOOD: 4 lb. Aug 25, 2020 · Sunshine Mills, Inc. Food and Drug Administration (FDA) reviewed your website at the Internet address www What are SSFFC? Drug recall versus drug withdrawal. Current recall data used in this Dashboard is based upon the Enforcement Reports. Food and Drug Administration Search Menu; 2020 Recalls (XML) 2019 Recalls (XML) FDA Recall Operations Team Leader Armando Zamora, explains how FDA manages product recalls. This is the latest This recall has been completed and FDA has terminated this recall. or submit by fax to 1-800-FDA This recall has been completed and FDA has terminated this recall. NEW! Medical Device Recalls and Reports of Corrections and Removals, Part 7, Part 806: Frequently Asked Questions Nov 5, 2024 · U. ’s voluntary recall of Saniderm Advanced Hand Sanitizer. Español. due to the Potential Risk of Salmonella Previous Major Three Recalls Designated as Class I by FDA; One Designated as Class … 2020 , have been designated as Class I recalls by the U. D. About PROGRAF® 0. Dec 30, 2020 · Flowers Foods, Inc. Aurobindo Pharma Limited is voluntarily recalling 22 Batches of the drug substance Irbesartan due to the presence of an impurity, N-nitrosodiethylamine (NDEA). Nov 2, 2020 · Nostrum Laboratories, Inc. Nostrum Laboratories, Inc. 4, 2020, has been designated as a Class I recall by the U. Nov 29, 2023 · In 2020, the FDA recalled two brands of the diabetes drug metformin that contained amounts of a cancer-causing agent called NDMA. Oct 1, 2024 · Information on Recalls of FDA Regulated Products OII Recall Coordinators. Contains Nonbinding Recommendations . Lubricant Eye Drops 15 ml (single pack) Carboxymethylcellulose Sodium 0. of Bakersfield, California is recalling Red, Yellow, White, and Sweet Yellow Onions shipped from May 1, 2020 through the present. Moreover, the toll on human life has been substantial. Illustrating the financial cost of recalls, Johnson and Johnson lost approximately $600 million in sales after closing a distribution site due to a recall. is issuing a voluntary recall of Nature’s Menu® Super Premium Dog Food with a Blend of Real Chicken & Quail because of the potential to be contaminated with Salmonella. [Posted 04/01/2020] ISSUE: The FDA announced it is requesting manufacturers to withdraw all prescription and over-the-counter (OTC) ranitidine drugs from the market immediately. (“Taro” or the “Company”) is voluntarily recalling two (2) lots of Phenytoin Oral Suspension USP, 125 mg/5 mL both in 237 mL bottles, to the consumer level. mzpdm enpxq xfxr eel faefmd hlrr zyzpsly okeni zipda ecp