Safety Alerts & Recalls

Search all Safety Alerts & Recalls

Latest Alerts

Recall on Ranbaxy's Generic Nitrofurantoin
The generic manufacturer Ranbaxy Pharmaceuticals Inc. announced that it is conducting a voluntary recall of all of their lots of nitrofurantoin (monohydrate/macrocrystals) capsules 100 mg currently on the market in the U.S. Nitrofurantoin is an antibiotic commonly used to treat urinary tract infections. Ranbaxy is recalling their nitrofurantoin product because it does not meet manufacturing standards. For more information, please visit: http://www.ranbaxy.com/news/newsdisp.aspx?cp=921&flag=ARC
Learn More

Recall on Single lot of Calan (Verapamil) 80 mg tablets
Pfizer has announced a recall of a single lot of Calan (verapamil hydrochloride) tablets 80 mg (NDC # 0025-1851-31), a medication commonly used to treat high blood pressure. Lot number C061194, expiration date December 2010 is being recalled because it does not meet manufacturing standards. For more information, please visit: http://www.fda.gov/Safety/Recalls/EnforcementReports/ucm157384.htm
Learn More

Date Published Title Drug Source
2009-05-04 Recall on Ranbaxy's Generic Nitrofurantoin Nitrofurantoin FDA
2009-05-04 Recall on Single lot of Calan (Verapamil) 80 mg tablets Verapamil FDA
2009-05-04 FDA Requires Additional Labeling for Over-the-Counter Pain Relievers and Fever Reducers FDA
2009-05-04 FDA Requires Additional Labeling for Over-the-Counter Pain Relievers and Fever Reducers FDA
2009-05-04 FDA Requires Additional Labeling for Over-the-Counter Pain Relievers and Fever Reducers Acetaminophen with Oxycodone FDA
2009-05-04 FDA Requires Additional Labeling for Over-the-Counter Pain Relievers and Fever Reducers Hydrocodone with Acetaminophen FDA
2009-05-04 FDA Requires Additional Labeling for Over-the-Counter Pain Relievers and Fever Reducers Butalbital, Acetaminophen & Caffeine FDA
2009-05-04 FDA Requires Additional Labeling for Over-the-Counter Pain Relievers and Fever Reducers FDA
2009-05-04 FDA Requires Additional Labeling for Over-the-Counter Pain Relievers and Fever Reducers FDA
2009-05-04 FDA Requires Additional Labeling for Over-the-Counter Pain Relievers and Fever Reducers FDA
2009-05-04 FDA Requires Additional Labeling for Over-the-Counter Pain Relievers and Fever Reducers Acetaminophen with Caffeine / Dihydrocodeine FDA
2009-05-04 FDA Requires Additional Labeling for Over-the-Counter Pain Relievers and Fever Reducers FDA
2009-05-04 FDA Requires Additional Labeling for Over-the-Counter Pain Relievers and Fever Reducers FDA
2009-05-04 FDA Requires Additional Labeling for Over-the-Counter Pain Relievers and Fever Reducers FDA
2009-05-04 New FDA Labeling for OTC Pain Relievers Also Applies to Patients Taking Combination Products Butalbital / Aspirin / Caffeine FDA
2009-05-04 New FDA Labeling for OTC Pain Relievers Also Applies to Patients Taking Combination Products Soma Compound with Codeine FDA
2009-05-04 New FDA Labeling for OTC Pain Relievers Also Applies to Patients Taking Combination Products Carisoprodol with Aspirin FDA
2009-05-04 New FDA Labeling for OTC Pain Relievers Also Applies to Patients Taking Combination Products Ibuprofen with Propoxyphene FDA
2009-05-04 New FDA Labeling for OTC Pain Relievers Also Applies to Patients Taking Combination Products Ibuprofen with Pseudoephedrine FDA
2009-05-04 New FDA Labeling for OTC Pain Relievers Also Applies to Patients Taking Combination Products FDA