Safety Alerts & Recalls

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Latest Alerts

Sertraline 100 mg Tablets: Single Lot Recalled
Aurobindo Pharma Limited is recalling a single lots of Sertraline Hydrochloride Tablets, 100 mg. Lot number SR1009068-A is being recalled because a tablet of Zolpidem Tartrate, 10 mg was found in a bottle from this lot. Sertraline is used in the treatment of depression, anxiety, and other mood disorders. Sertraline is also sold under the brand name Zoloft. No other lots, strengths, or brands of sertraline were involved in this recall. To view the FDA notice about this recall, please visit: http://www.fda.gov/Safety/Recalls/EnforcementReports/ucm217780.htm
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Zolpidem: Two Lots Recalled Because of Oversized Tablets
Aurobindo Pharma Limited is recalling two lots of Zolpidem Tartrate Tablets, 10 mg. Lot numbers ZT1009034-A and ZT1009036-A are being recalled because an oversized tablet was found in these lots. Zolpidem is used in the treatment of insomnia and is also sold under the brand name Ambien and Ambien CR. No other lots, strengths, or brands of zolpidem were involved in this recall. To view the FDA notice about this recall, please visit: http://www.fda.gov/Safety/Recalls/EnforcementReports/ucm217780.htm
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Date Published Title Drug Source
2010-07-21 Sertraline 100 mg Tablets: Single Lot Recalled Sertraline FDA
2010-07-21 Zolpidem: Two Lots Recalled Because of Oversized Tablets Zolpidem FDA
2010-07-21 Little Tummy's Stimulant Laxative Drops: Manufacturer Recalls Four Lots Senna FDA
2010-07-21 Ortho-McNeil Pharmaceutical, Inc. Recalls Select Lots of Ultram ER (tramadol HCl) Extended-Release Tablets, 100 mg Tramadol FDA
2010-07-21 Itch Relief Eye Drops Recalled from Popular Store Brands (Target, Walgreens, CVS, Kroger, H-E-B and Others) Ketotifen FDA
2010-07-20 Amoxicillin for Oral Suspension: Recall by Teva Pharmaceuticals Amoxicillin FDA
2010-07-20 Select Lots of Nifediac CC Extended Release 60 mg Tablets Recalled By Biovail Pharmaceuticals Nifedipine FDA
2010-07-20 Paroxetine 40 mg Tablets: Single Lot Recalled by Aurobindo Pharma Paroxetine FDA
2010-07-20 Tretinoin Cream: Three lots recalled by Ortho Pharmaceutical Tretinoin FDA
2010-07-20 Recall of Two Lots of Sulfacetamide Sodium Topical Suspension Sulfacetamide FDA
2010-07-20 Clear Nicotine Patch 7 mg, 14 mg, and 21 mg Recalled At Warehouse/Retail Level Nicotine FDA
2010-07-20 Lorazepam 0.5 mg Tablets: Sandoz Recalls Single Lot Lorazepam FDA
2010-07-20 Quixin: Recall of Two Lots Levofloxacin FDA
2010-07-16 Stolen Advair Inhalers Appear in Pharmacies Fluticasone Propionate with Salmeterol FDA
2010-07-16 FDA Announces Ongoing Safety Review of Angiotensin Receptor Blockers (ARBs) for Cancer Risk Telmisartan FDA
2010-07-13 Leflunomide (Arava): FDA Adds Information on Severe Liver Injury to the Boxed Warning Leflunomide FDA
2010-07-11 McNeil Expands Recall To Include Additional Lots of Benadryl Allergy Ultratab, Children's Tylenol Meltaways, Motrin, IB, Tylenol Extra Strength, and Tylenol PM Acetaminophen with Diphenhydramine Hydrochloride Manufacturer
2010-07-09 McNeil Expands Recall To Include Additional Lots of Benadryl Allergy Ultratab, Children's Tylenol Meltaways, Motrin, IB, Tylenol Extra Strength, and Tylenol PM Ibuprofen Manufacturer
2010-07-09 FDA Warns Using Malaria Medication for Leg Cramps Can Lead to Serious Side Effects Quinine Sulfate FDA
2010-07-06 Bristol-Myers Recalls Coumadin Blister Pack Samples Warfarin Manufacturer