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Recall
Teva Pharmaceuticals USA, Inc. Initiates Voluntary Nationwide Recall of Metformin Hydrochloride
PR-M06-20-NI-025
Recall
Takeda Issues US Recall of Two Lots of VONVENDI
PR-M02-20-NI-038
Recall
FDA Updates and Press Announcements on NDMA in Zantac (ranitidine)
PR-M10-19-NI-047
Recall
Torrent Pharmaceuticals Limited Expands Voluntary Nationwide Recall of Losartan Potassium Tablets
PR-M09-19-NI-055
Recall
FDA Announces Voluntary Recall of Sandoz Ranitidine Capsules Following Detection of an Impurity
PR-M09-19-NI-049
Recall
Pacifico National, Inc. dba AmEx Pharmacy Issues Voluntary Nationwide Recall for all Lots of Bevacizumab
Recall
Pfizer Inc. Issues A Voluntary Nationwide Recall For 2 Lots of RELPAX® Due to Potential Microbiological Contamination of Non-Sterile Product
PR-M08-19-NI-048
Recall
FDA Requests Allergan Voluntarily Recall Certain Breast Implants and Tissue Expanders from Market
PR-M07-19-NI-071
Recall
Bayer Statement on Voluntary Recall of Two Lots of Kogenate® FS Antihemophilic Factor (Recombinant) in the United States
PR-M07-19-NI-062
Recall
Altaire Pharmaceuticals, Inc. Issues Voluntary Recall of Multiple Ophthalmic Products
PR-M07-19-NI-036
Recall
Mylan Institutional LLC Initiates Voluntary Nationwide Recall of Levoleucovorin Injection Due to the Presence of Particulate Matter
PR-M03-19-NI-050
Drug Recall
FDA Provides Update on its Ongoing Investigation into ARB Drug Products and Losartan Product Recall
PR-M03-19-NI-001
Recall
Mylan Initiates Voluntary Nationwide Recall Due to the Detection of Trace Amounts of NDEA
PR-M11-18-NI-087
Recall
Sandoz Issues Voluntary Recall of Losartan
PAO-M11-18-NI-016
Pediatric
Incorrect Dosing Cup Leads to Recall of Children’s Advil Suspension
PAO-M09-18-NI-005
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