Recalls and Notices

Some medicines and medical devices are dangerous when misused.  Others may turn out to be inherently dangerous.  It's crucial that healthcare providers be aware of all current drug warnings, FDA recalls, public health notices and other drug/product safety information.  That information can be found here.

 
 Date PostedPublication
5/24/2019 Pharm D Solutions, LCC Issues Voluntary Nationwide Recall of All Sterile Compounded Drugs Due to a Potential Lack of Sterility 
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5/14/2019 Novartis Issues Voluntary Nationwide Recall of Promacta 12.5 mg for Oral Suspension Due to Potential Peanut Contamination 
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5/6/2019 Par Pharmaceutical, Inc. Issues Recall for One Lot of Mycophenolate Mofetil for Injection, USP due to the Presence of Glass Fragments 
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5/1/2019 Voluntary Nationwide Recall of Ketorolac Due to Lack of Sterility Assurance 
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4/22/2019 Alvogen Inc. Issues Voluntary Nationwide Recall of Fentanyl Transdermal System Due to Product Mislabeling 
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4/19/2019 Additional Expansion to Torrent Pharmaceuticals Recall of Losartan Potassium Tablets, USP and Losartan Potassium/Hydrochlorothiazide Tablets, USP 
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4/1/2019 Legacy Pharmaceutical Packaging, LLC Recalls Losartan Potassium Tablets, USP, 25mg, 50mg, 100mg - Expanded Recall 
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3/21/2019 Mylan Institutional LLC Initiates Voluntary Recall of Levoleucovorin Injection Due to the Presence of Particulate Matter 
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3/18/2019 Hospira, Inc. Issues Recall of 8.4% Sodium Bicarbonate Injection, USP due to the Presence of Particulate Matter 
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3/18/2019 Legacy Pharmaceuticals Packaging, LLC Issues Recall of Losartan Potassium Tablets, USP 50mg due to NMBA Impurity 
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3/8/2019 American Health Packaging Issues Voluntary Nationwide Recall of Valsartan Tablets Due to NDEA Impurity 
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3/1/2019 AurobindoPharma USA Inc., Issues Recall Expansion of 38 Lots of Amlodipine Valsartan Tablets USP and Valsartan Tablets USP 
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3/1/2019 Camber Pharmaceuticals, Inc. Issues Voluntary Recall of Losartan Potassium Tablets, USP 25 mg, 50mg, and 100mg, due to Detection of NMBA Impurity 
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2/27/2019 Physio-Control Recalls LIFEPAK 15 Monitor/Defibrillator Due to Risk of Device "Lockup" (Freezing)  
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2/25/2019 Macleods Pharmaceuticals Limited Issues Voluntary Recall for One Lot (BLM 715A) of Losartan/HCTZ Combination Tables 100mg/25mg Due to Impurity.  
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2/4/2019 Sterile Saline and Sterile Water for Inhalation Recalled Due to Potential Exposure to Infectious Agents 
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1/23/2019 Updated: Torrent Pharmaceuticals Recall of Losartan Potassium Tablets, USP and Losartan Potassium and HCTZ Tablets USP 
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1/23/2019 Losartan Products under Recall 
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1/18/2019 Prinston Pharmaceutical Inc. Issues Voluntary Recall of Irbesartan and Irbesartan HCTZ Tablets due to Impurity 
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1/8/2019 Lupin Pharmaceuticals, Inc. Issues Voluntary Recall of Ceftriaxone for Injection USP 
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