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
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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1/2/2019 Aurobinda Pharma USA, Inc. Initiates Voluntary Nationwide Recall of Multiple Products 
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12/21/2018 Terrific Care, LLC./Medex Supply Dist., Inc. Issues Nationwide Recall of CoaguChek Test Strips 
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12/20/2018 Enovachem Pharmaceuticals Issues Voluntary Nationwide Recall of Dyural-40 and Dyural-80 Convenience Kits Containing Recalled Sodium Chloride Injection, USP 0.9% Due to Latex Hazard 
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12/13/2018 GE Healthcare Recalls CareScape R860 Inspiratory Safety Guard Due to Risk of Disconnection from Breathing Circuit 
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12/10/2018 FDA Alerts Health Care Professional and Patients Not to Use Drug Products Intended to be Sterile from Promise Pharmacy 
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12/10/2018 Mylan Expands it's Voluntary Nationwide Recall of Various Tablets Containing Valsartan  
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11/27/2018 Teva Pharmaceuticals USA Issues Voluntary Nationwide Recall of All Amlodipine/Valsartan and Amlodipine/Valsartan/Hydrochlorothiazide Combination Tablets 
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11/23/2018 Mylan Initiates Voluntary Nationwide Recall of Various Tables Containing Valsartan 
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11/23/2018 Fresenius Kabi Issues Voluntary Nationwide Recall of Sodium Chloride Injection, USP, 0.9% 
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11/21/2018 FDA Alerts Health Care Professional and Patients Not to Use Sterile Drug Products from Pharm D Solutions 
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11/9/2018 Sandoz Inc. Issues Voluntary Nationwide Recall of One Lot of Losartan Potassium and Hydrochlorothiazide 
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11/9/2018 Kadesh Inc. Issues Voluntary Nationwide Recall of Puriton Eye Relief Drops 
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11/5/2018 FDA Alerts Patients and Health Care Professionals That Some EpiPen Auto Injectors May Not Easily Slide Out of Carrier Tube 
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11/2/2018 Roche Diagnostics Recalls CoaguChek XS PT Test Strips due to Inaccurate INR Test Results 
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11/1/2018 Aurobindo Pharma Limited Issues Voluntary Recall of Irbesartan Drug Substance due to the Detection of Trace Amounts of NDEA Impurity 
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10/22/2018 Promise Pharmacy Issues Voluntary Nationwide Recall of Prednisolone and Gatifloxacin Ophthalmic Solution 1%/0.5% Sterile Due to Small Particulate Floating in the Solution 
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10/15/2018 Endologix, Inc. Recalls AFX Endovascular AAA Systems Due to Risk of Type III Endoleaks 
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10/1/2018 Edno Pharmaceuticals Issues Voluntary Nationwide Recall for Two Lots of Robaxin 750mg Tablets 100 Count Bottle Packs Due to Incorrect Daily Dosing Information 
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