Summary Company Announcement Date: December 07, 2018 FDA Publish Date: April 23, 2019 Reason for Announcement: Recall Reason Food & Beverage Safety, Unapproved Ingredient Company Name: J.M Smuckers Company Brand Name: Brand Name(s) Product Description: Product Description Company Announcement The J.M. Smucker Company today … [Read more...]
Teva Pharmaceuticals USA, Inc. Issues Voluntary Nationwide Recall of Losartan Potassium 25 mg and 100 mg Tablets USP, Sold Exclusively to Golden State Medical Supply
GSMS FG NDCs GSMS FGNDC Description GSMS FG Product Lots GSMS FG Expiration Dates 60429-318-90 Losartan Potassium, Tablets, USP, 100 mg, 90 Count Bottle GS014045 06/2019 60429-318-90 Losartan Potassium, Tablets, USP, 100 mg, 90 Count Bottle GS014305 06/2019 60429-318-10 Losartan Potassium, Tablets, USP, 100 mg, 1,000 Count … [Read more...]
Legacy Pharmaceutical Packaging, LLC Expands Voluntary Nationwide Recall of Losartan Potassium Tablets, USP, 50mg Due to the Detection of Trace Amounts of N-Nitroso N-Methyl 4-amino butyric acid (NMBA) Impurity Found in the Active Pharmaceutical Ingredient (API)
Legacy Pharmaceutical Packaging, LLC is expanding its consumer-level recall of 3 repackaged lots Losartan Tablets USP 50mg to include one additional lot. This recall was prompted due to Torrent Pharmaceuticals LTD issuing a Voluntary Nationwide Recall of Losartan Tablets, USP, due to the detection of trace amounts of N-Nitroso N-Methyl 4-amino … [Read more...]
Jurox Incorporated is Voluntarily Recalling Two Lots of Alfaxan Unpreserved, an Intravenous Injectable Anaesthetic
Vial size Lot Number Distributed from Expiry 10mL #27787 April 2017 March 2020 10mL #25955 October 2016 August 2019 This recall has been initiated due to an out of specification result for clarity observed in the stability program. The presence of the aluminum phosphate precipitate presents a potential risk that intravascular (I.V.) injection of … [Read more...]
Alvogen Inc. Issues Voluntary Nationwide Recall of Fentanyl Transdermal System Due to Product Mislabeling
Alvogen, Inc. is voluntarily recalling two lots of Fentanyl Transdermal System 12 mcg/h transdermal patches to the consumer level. A small number of cartons labeled 12 mcg/h Fentanyl Transdermal System patches contained 50 mcg/h patches. The 50 mcg/h patches that were included in cartons labeled 12 mcg/h are individually labeled as 50 mcg/h. This … [Read more...]
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