Drug and Medicine Product Recalls and Safety Alerts

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Drug and Medicine Recalls and Alerts

0 - 49 of 1039 Drug and Medicine recalls/alerts

1/23/2007

Ebek, Inc. Issues Voluntary Nationwide Recall of Liviro3, a Product Marketed as a Dietary Supplement

12/28/2006

Alcon Announces Voluntary Recall of Systane Free LIQUID GEL Lubricant Eye Drops in the United States, Including Puerto Rico

12/28/2006

Boston Scientific Announces Nationwide Recall of 51 Mach 1 Guide Catheters

11/28/2006

Rockline Announces Voluntary Product Withdrawal of Wet Wipes Products

11/28/2006

Advanced Medical Optics Announces Voluntary Recall of 18 Lots of Complete(R) MoisturePLUS(TM) Contact Lens Care Products Distributed and Sold in the U.S.

10/17/2006

FDA Issues Nationwide Alert on Counterfeit One Touch Basic/Profile and One Touch Ultra Blood Glucose Test Strips

9/21/2006

Nasutra, LLC Issues a Voluntary Nationwide Recall of Nasutra, a Product Marketed as a Dietary Supplement To Support Male Sexual Performance, Due to Unlisted, Potentially Hazardous Ingredient

9/20/2006

Orth Evra Labeling Information Changed

9/8/2006

Ibuprofen and Aspirin Take Together

8/11/2006

The Mentholatum Company Issues a Nationwide Voluntary Recall of WellPatch Cough & Cold Soothing Vapor Pads in the U.S.

7/14/2006

Roxane Laboratories Initiates a Nationwide Voluntary Recall of a Single Manufacturing Lot of Azathioprine Tablets in the U.S. and Puerto Rico

7/14/2006

Disetronic Medical Systems Inc Announces a Voluntary Nationwide Recall of Disetronic D-TRONplus Power Packs used in D-TRON plus Insulin Pumps

7/7/2006

Boston Scientific Announces Faulty Battery in Certain Defibrullator Devices

7/7/2006

MRL, Inc. Issues a Voluntary Worldwide Recall of Selected PIC50 External Monitor/Defibrillators

6/19/2006

Novartis Consumer Health Conducts Nationwide Voluntary Recall of Triaminic Vapor Patch Product in U.S.

6/19/2006

MRL, Inc., Issues a Voluntary Worldwide Recall of Selected AED20 Automatic External Defibrillators

6/12/2006

Hamilton Medical Issues a Medical Device Safety Alert on certain RAPHAEL Ventilators

6/12/2006

Hamilton Medical Issues a Medical Device Safety Alert on certain RAPHAEL Ventilators

5/25/2006

Spectrum Laboratory Products, Inc. Issues Nationwide Recall of Tacrolimus Active Pharmaceutical Ingredient

5/15/2006

Bausch & Lomb Pulls ReNu With Moisturloc Lens-Solution

5/4/2006

IVAX Pharmaceuticals Issues a Nationwide Recall of Goldline Brand Extra Strength Genapap and Extra Strength Genebs

5/1/2006

Ortho-Clinical Diagnostics Issues Class I Recall on Vitros Immunodiagnostic Products

5/1/2006

Oxygen Regulator Fires Resulting from Incorrect Use of CGA 870 Seals

5/1/2006

The FDA Issues Alert on Phernergan

5/1/2006

FDA Issues Public Health Notification on Baxter's Colleage Infusion Pumps

5/1/2006

Pascal Company, Inc. recalls all lots and all flavors of NeutraGard 0.05% Neutral Sodium Fluoride Anticavity Treatment Rinse and NeutraGard Plus 0.2% Neutral Sodium Fluoride Anticavity Treatment Rinse

4/17/2006

Blackstone Medical, Inc. Issues Voluntary Recall of ICON(tm) Modular Fixation System

4/17/2006

Boca Medical Products, Inc. Issues Nationwide Recall of Insulin Syringe Product

4/11/2006

Serious Eye Infections Associated With Soft Contact Lens Use and Bausch & Lomb's ReNu Moistureloc

4/5/2006

The FDA Issues a Public Health Advisory on Diastat AcuDial Diazepam Rectal Gel

4/5/2006

Disetronic Medical Systems, Inc. Announces a Voluntary Nationwide Recall Of ALL ACCU-CHEK Ultraflex Infusion Sets

4/3/2006

Ossur Announces Voluntary Recall of Certain Models of the Total Knee

3/24/2006

FDA Issues Guidance on Hospital Bed Design to Reduce Patient Entrapment

3/23/2006

FDA Warns Manufacturers About Illegal Steroid Products Sold as Dietary Supplements

3/23/2006

Ligand Pharmaceuticals and the FDA Changes Ontak Labeling

3/23/2006

FDA Issues Public Health Advisory on Mifeprex

3/3/2006

Class 1 Recall of Bard Composix Kugel Mesh X-Large Patch Oval Used to Repair Hernias

3/3/2006

FDA Issues Update of Information About BioMedical Tissue Services

3/3/2006

Actelion Updates Tracleer Labeling

3/1/2006

Hanford Pharmaceuticals Issues a Nationwide Recall of Cefazolin for Injection Because of Possible Health Risk

2/22/2006

Bayer Adds Warning to Nimotop Label

2/22/2006

Bristol Myers Squibb Proposes Changes to Tequin Label

2/14/2006

FDA Requests Recall of Balanced Salt Solution

2/3/2006

FDA, Boston Scientific Recalls Flextome Cutting Balloon Systems

1/26/2006

Vapotherm Issues Urgent Nationwide Recall Of All Vapotherm 2000i Respiratory Gas Humidification Devices

1/20/2006

FDA Approves Updated Labeling for Elidel and Protopic

1/20/2006

FDA Issues Public Health Advisory on Ketek Tablets

1/18/2006

Novartis and FDA Notifies Doctors and Patients to Revisions to the Boxed Warnings for Clozaril Tablets.

1/18/2006

FDA Warns Consumers about Brazilian Diet Pills Found to Contain Active Drug Ingredients

1/18/2006

Roche Diagnostics Issues a Worldwide Voluntary Recall of Some of its ACCU-CHEK Aviva Meters

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