- AS Medications Solution LLC. Announces a Nationwide Recall of All Lots of Digoxin Tablets 0.25mg Due to Size Variability
- Disetronic Medical Systems Inc.Announces a recall of the ACCU-CHEK Spirit insulin pump due to "up" and/or "down" butto
- Neilgen Pharma Inc. and Advent Pharmaceutical Recall All Prescription Cough and Cold Drug Products Sold on or after Marc
- FDA Statement on the Voluntary Withdrawal of Raptiva From the U.S. Market
- FDA Works With Drugmakers to Increase Oxycodone Production
- Digoxin Recall made by CARACO pharm.
- Watson Announces a Nationwide Voluntary Recall of Propafenone HCL Tablets Due to Oversized Tablets (March 23)
- Non-safety-related voluntary market withdrawal of a limited portion of DAYTRANA (methylphenidate transdermal system) pat
- Ther-Rx Corporation Issues Voluntary Nationwide Recall Of Prescription Prenatal and Iron Supplements To Wholesale Level
- ETHEX Corporation Issues Voluntary Nationwide Recall Of Prescription Prenatal and Iron Supplements To Wholesale Level (
- ETHEX Corporation Issues Voluntary Nationwide Recall (February 3)
- KV Pharmaceutical Voluntarily Suspends All Shipments of its Approved Tablet-form Drugs (December 23)
- FDA Warns Consumers About Tainted Weight Loss Pills (December 22)
- Genentech issues 2nd "Dear Healthcare Provider letter" re: PML with Raptiva
- Johnson and Johnson--Merck Consumer Pharmaceuticals Company Announces Urgent Voluntary Nationwide Recall Of Infants' Myl
- ETHEX Corporation Initiated Nationwide Voluntary Recalls of Specific Lots of Five Generic Products Due to the Potential
- FDA Reports Nationwide Recall of Mislabeled ReliOn Insulin Syringes (November 5)
- FDA Warns Consumers About Potential Problems at Two Baltimore Pharmacies
- Actavis Totowa Announces Voluntary Recall at the Retail Level of All Drug Products Manufactured at its Little Falls, New
- Roxane Laboratories, Inc. Initiates a Nationwide Voluntary Recall of Two Manufacturing Lots of Sodium Polystyrene Sulfon
- Sage Products Inc. Issues Voluntary Recall of 2% Chlorhexidine Gluconate Cloth Patient Preoperative Skin Preparation (Ju
- ETHEX Corporation Voluntarily Recalls Specific Lots of 30 mg. and 60 mg. Morphine Sulfate Extended Release Tablets Due t
- ETHEX Corporation Voluntarily Recalls a Single Lot of Morphine Sulfate 60 mg Extended Release Tablets Due to the Potenti
- Actavis Totowa (formerly known as Amide Pharmaceutical, Inc.) recalls all lots of Bertek and UDL Laboratories Digitek (d
- Herbal Science International, Inc. Recalls Twelve Dietary Herbal Supplements Nationwide Because of Possible Health Risk
- Actavis Recalls Remaining Fentanyl Patches in the US as Precaution (Mar. 1)
- Baxter to Proceed with Recall of Remaining Heparin Sodium Vial Products (Feb. 28)
- PriCara Recalls 25 mcg/hr DURAGESIC (fentanyl transdermal system) CII Pain Patches (F