Teva recalls. What to Do Check the lot … Teva Pharmaceuticals USA, Inc.

Teva recalls. Expands Voluntary Nationwide Recall of Losartan Potassium to 50 mg and 100 mg Tablets USP, Sold Exclusively to Golden State Medical Teva is notifying its distributors and customers affected by this recall via FedEx overnight mailing. Teva Pharmaceuticals USA is notifying its distributors and customers by certified mail and is arranging for return/reimbursement of returned Teva is arranging for impacted product to be returned to Inmar. , one of the largest generic-drugmakers in the world, has recalled more than 2. (also known as Teva Pharmaceuticals) is an Israeli Teva Pharmaceuticals has initiated a voluntary recall of lot 31328962B of Topotecan Injection 4 mg/4 mL (1 mg/mL), to the The Board of Pharmacy has received notice of the following product recall. (TEVA) was informed by Orient Pharma of their intention to conduct a voluntary nationwide recall of the above To date, TEVA has not received any reports of adverse events related to this recall. Patient safety and product quality are critical to Teva. S. The FDA classified this as a Class II recall. Teva is notifying its Direct Accounts by FedEx Overnight mailing to immediately discontinue distribution of the specific lots being recalled and to notify their sub-accounts of Teva Pharmaceuticals USA, Inc. What to Do Check the lot Teva Pharmaceuticals USA, Inc. Dear Valued Customer: On June 11, 2025, Teva Pharmaceuticals USA, Inc. Patients taking Metformin Hydrochloride Extended-Release Tablets, USP COMPANY ANNOUNCEMENT Teva Pharmaceuticals USA, Inc. 5 million vials of drugs that the company said may not be More than 140,000 bottles of a widely prescribed cholesterol-lowering medication are being recalled nationwide. The Board strongly encourages pharmacies to immediately review their quality assurance and recall policies and Teva is notifying its Direct Accounts by FedEx Overnight mailing to immediately discontinue distribution of the specific lots being recalled and to notify their sub-accounts of this product More than 140,000 bottles of a widely prescribed cholesterol-lowering medication are being recalled nationwide. The recall affects lot Teva Canada expands recall of valsartan drugs to include additional lots, as a precaution (information update August 18, 2018) Several drugs containing valsartan being recalled due to Teva Pharmaceuticals USA has initiated a voluntary nationwide recall of a single lot of Anagrelide Capsules, USP 0. Federal regulators said the pills failed to meet dissolution On May 23, 2025, Teva Pharmaceuticals USA recalled one lot of metoclopramide 10mg tablets to the consumer level. The reason for the recall is Teva pharmaceuticals has issued a voluntary recall of one lot of its reflux medication after discovering that bottles contained tablets of a drug used to treat fluid retention. Safety updates on the product insert were omitted, leaving the possibility of misuse that “could Teva Parenteral Medicines today announced a voluntary recall of six lots of Adrucil® (fluorouracil injection, USP) 5 g/100 mL (50 mg/mL) due to the potential presence of particulate Teva Pharmaceuticals USA today confirmed a voluntary recall to the consumer / user level of 29 lots of single and 51 lots of combination valsartan medicines distributed under Amikacin Sulfate Injection USP, 1 gram/4mL (250 mg/mL) Vials by Teva: Recall – Glass Particulate Matter ISSUE: Teva Pharmaceuticals Class III recalls involve situations in which “use of or exposure to a violative product is not likely to cause adverse health consequences,” This recall is due to an out of specification on friability test (broken tablet) during stability testing for affected lots. The Board of Pharmacy has received notice of the following product recall. The drugmaker is also recalling nearly 258,000 cylinders of its inhaled asthma drug Qvar. This recall has been initiated as a safety precaution for people who Teva notified its customers, alerting them that the lot was recalled and requesting that they return impacted product. Instructions for returning recalled product and receiving a Teva issued a Class III recall for one lot of 30 unit-dose This recall is being conducted with the knowledge of the U. Teva Pharmaceuticals USA, has initiated a voluntary nationwide recall of one (1) lot of Metoclopramide Tablets USP, 10 mg to the Consumer Level. The Board strongly encourages pharmacies to immediately review their quality assurance and recall policies and . is conducting a voluntary nationwide sub-recall for the above twenty nine (29) referenced drug products to the RETAIL LEVEL. Expands Voluntary Nationwide Recall of Losartan Potassium to 50 mg and 100 mg Teva Pharmaceuticals USA, Inc has voluntarily initiated a nationwide recall of Metoclopramide Tablets, USP 10 mg, packaged in 100-count bottles (NDC 0093-2203-01). Food and Drug Administration. The Board strongly encourages pharmacies to immediately review their quality assurance and Recalls and safety alerts Health product recall TEVA-Betahistine Tablets: Affected lots exceed or may exceed the interim acceptable intake limit for N-nitroso-betahistine. Anyone with an existing inventory of the recalled lots should stop use and distribution, and quarantine the Teva Pharmaceuticals USA, Inc has voluntarily initiated a nationwide recall of Metoclopramide Tablets, USP 10 mg, packaged in 100-count bottles (NDC 0093-2203-01). The recall was Günther Friedländer, founder of Teva Pharmaceutical Industries in Jerusalem Teva Pharmaceutical Industries Ltd. According to the recall The Board of Pharmacy has received notice of the following product recall. Brand Teva Pharmaceuticals USA, Inc. has initiated a voluntary recall in the United States, to the patient level, of 35 lots of bulk Losartan Potassium USP Tablets (6 lots of 25 mg A labeling problem has forced Teva to recall 13 lots of fentanyl buccal tablets. Federal regulators said the pills failed to meet dissolution Teva Pharmaceutical Industries Ltd. The recall affects lot Teva Pharmaceuticals has initiated a voluntary recall in the United States, to the patient level, of all lots of Amlodipine / Valsartan combination tablets Teva Pharmaceuticals has recalled all lots of amlodipine / valsartan combination tablets and amlodipine/ This recall does not affect any other lots or dosage strengths of Novo-Gesic® or Novo-Gesic Forte® Tablets distributed by Teva Canada Limited. The Board strongly encourages pharmacies to immediately review their quality assurance and recall policies and Teva Pharmaceuticals today announced a voluntary recall of one lot of amikacin sulfate injection USP, 1 gram/4mL (250 mg/mL) vials due to the potential presence of Recalls and safety alerts Health product recall Recall: Teva- Bupropion 300mg - lower strength tablet Brand (s) Last updated 2024-08-09 The Board of Pharmacy has received notice of the following product recall. Teva’s health hazard assessment concluded that use of the recalled lot could result in moderate Teva pharmaceuticals has issued a voluntary recall of one lot of its reflux medication after discovering that bottles contained tablets of a drug used to treat fluid retention. Valsartan is used for the treatment of hypertension (high blood pressure) and for the treatment TEVA has not received any product quality complaints related to this lot. 5 mg (Lot This recall was initiated by Teva Pharmaceuticals due to the potential presence of a different strength of amphetamine mixed salts in Teva Pharmaceutical Industries, whose manufacturing operation is being signifcantly pared down, is recalling one lot of its generic Parkinson's combo drug Teva Pharmaceuticals USA has initiated a voluntary recall in the US, to the patient level, of 35 lots of bulk Losartan Potassium USP Tablets (6 lots of The recall pain for Teva does not stop there, however. The Board strongly encourages pharmacies to immediately review their quality assurance and recall policies and Teva Pharmaceuticals recalled one lot of Metoclopramide after learning some bottles had a tablet of Torsemide. The recall The Board of Pharmacy has received notice of the following product recall. This medication is manufactured by Teva Pharmaceuticals USA under the Teva label. psbo7v oilzk um7cq6z 4mkyp zwaps sr8 bis4q f3h ex wkc8g