Product Recall Archives

Mar 7
FDA Finds Contaminant in Recalled Heparin
At the end of January Baxter Healthcare issued a voluntary recall of specific batches of their heparin products due to reports of adverse events. On Wednesday the U.S. Food and Drug Administration announced that test had revealed a "heparin-like contaminant...
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Jan29
Baxter Issues Urgent Recall of Certain Lots of Heparin
Baxter Healthcare Corporation has issued an immediate voluntary recall of nine lots of heparin sodium injection 1000 units/ml and 30 ml multi-dose vials.The lots recalled are:NDC NUMBERS 0641-2440-45, 0641-2440-41, 0641-2450-45 and 0641-2450-41LOTS: 107054, 117085, 047056, 097081, 107024, 107064, 107066, 107074,... Continue Reading
Oct29
Wyeth Voluntary Recall of Some Robitussin and Children's Dimetapp Products
While there is no issue with the medication, Wyeth has initiated a voluntary recall and replacement for all U.S retail outlets concerning several Robitussin and Children's Dimetapp Cold and Chest Congestion products.The recall involves the removal of all products that... Continue Reading
Sep24
Axcil and Desirin Dietary Supplements Recalled
TWC Global LLC Inc. has issued an nationwide recall of its products Axcil and Desirin, which are marketed as dietary supplements, as they contain potentially harmful ingredients.The FDA found that the products contained sildenafil, the active ingredient of an FDA approved... Continue Reading
Sep19
Abbott Notifies Users of Blood Glucose Meters of Potential Screen Display Problems
Users of the following Abbott Laboratories manufactured glucose meters: Precision Xtra™, Optium™, ReliOn® Ultima, Rite Aid® and Kroger® are being warned that dropping the units on a hard surface could cause improper function of the display screens.  Units manufactured after January... Continue Reading
 


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