Fda medication recall list 2018
[PDF File]Recall Notice: Valsartan and Valsartan/HCTZ Products are ...
https://info.5y1.org/fda-medication-recall-list-2018_1_4c7033.html
Recall Notice: Valsartan and Valsartan/HCTZ Products are Recalled by FDA- July 2018 . The medication valsartan and the combination drug valsartan-hydrochlorothiazide (valsartan-hctz), from certain manufacturers, have been recalled by the U.S. Food and Drug Administration (FDA). The reason for this recall:
[PDF File]Drug Recall List
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Class 3 Recall: Using the drug is not likely to cause adverse health consequences. NOTE: This is not a complete list of all recalls. Please see FDA.gov >Drugs>Drug Safety and Availability> Drug Recalls for additional information. Drug Recall List Last Updated: July 2019 . Drug Recall Details Contact Date Drug Recall Class*
FDA announces more valsartan recalls, issues warning letter ...
FDA announces more valsartan recalls, arated out a list of products not under issues warning letter to API manufacturer The valsartan recalls continued in late 2018 when FDA alerted patients and health professionals that Teva Pharma-ceuticals issued a voluntary recall of valsartan-containing products manu-factured using active pharmaceutical
[PDF File]URGENT MEDICAL DEVICE RECALL
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ongoing by BD, FDA, and CDC. This recall only affects the product Catalog (REF) and lot numbers listed in Attachment A: List of Recall Catalog Numbers and Lot Numbers, all from a single manufacturing site. No products other than those listed in the Attachment A are affected by this recall.
FDA FACT SHEET
FDA FACT SHEET. Find the list on the following webpage: Search List of Recalled Angiotensin II Receptor Blockers (ARBs) including Valsartan, Losartan and Irbesartan
[PDF File]Valsartan and Valsartan- HCTZ Products – Recall Update
https://info.5y1.org/fda-medication-recall-list-2018_1_1d98e2.html
Valsartan and Valsartan- HCTZ Products – Recall Update • On July 27, 2018, the FDA announced that several additional companies that repackage drug products are also recalling valsartan and valsartan-HCTZ products. — On July 13th, the FDA initiated a series of announcements regarding the recall of certain
[PDF File]Recall Notice: Valsartan and Valsartan Combination Products ...
https://info.5y1.org/fda-medication-recall-list-2018_1_9aafbc.html
Recall Notice: Valsartan and Valsartan Combination Products are Recalled by FDA- Updates August 2018 The medication valsartan and the combination drugs valsartan-hydrochlorothiazide (valsartan-hctz) and valsartan-amlodipine-hydrochlorothiazide (amlodipine-valsartan-hctz) from certain manufacturers, have been recalled by the U.S. Food and Drug
[PDF File]URGENT DRUG RECALL NIFEdipine 10 mg Capsules, USP
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URGENT DRUG RECALL NIFEdipine 10 mg Capsules, USP October 6, 2016 Page 1 of 1 Dear Valued Customer: This is to advise you of a voluntary recall of 1-lot of NIFEdipine 10 mg Capsules, USP.
[PDF File]Orange Book March 2018 Changes List
https://info.5y1.org/fda-medication-recall-list-2018_1_5c4de1.html
Prescription and Over-the-Counter Drug Product List 38TH EDITION Cumulative Supplement Number 03 : March 2018 . ADDITIONS/DELETIONS FOR PRESCRIPTION DRUG PRODUCT LIST
[PDF File]Valsartan Recall – Update
https://info.5y1.org/fda-medication-recall-list-2018_1_7323f2.html
Valsartan Recall – Update • On September 13, 2018, the FDA announced an update to the ongoing investigation surrounding the recent voluntary recall of several drug products containing the active pharmaceutical ingredient (API) valsartan. • The FDA’s latest testing of products shows an additional unexpected impurity in three lots of
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