Product Recalls in Maine

Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,301 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,301 in last 12 months

Showing 4322143240 of 48,770 recalls

Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: MODULAR AUSTIN MOORE FENE. Item codes starting with 45502001 Recalled by...

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: MOORE HIP PROS LONG FENES Recalled by Zimmer, Inc. Due to Zimmer recently...

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: TRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System: One 1 g...

The Issue: Incorrect instructions for use (IFU).

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: TRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System Recalled by...

The Issue: Incorrect instructions for use (IFU).

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceOctober 11, 2013· GE Healthcare, LLC

Recalled Item: HGE Healthcare Patient Monitor B30 Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· GE Healthcare, LLC

Recalled Item: GE Vivid E9 ultrasound system. GE Vivid E9 is a Recalled by GE Healthcare,...

The Issue: GE became aware of a potential safety issue due to a system slow down and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT Computed Tomography X-Ray System Recalled by Philips Medical...

The Issue: If the couch, with the footrest extension attached, is positioned where the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· St. Jude Medical

Recalled Item: Safire Duo Ablation Catheter MediGuide Enabled Recalled by St. Jude Medical...

The Issue: St. Jude Medical Cardiovascular and Ablation Technologies Division is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi eXtreme ACCELERATOR Dietary Supplement Capsules Recalled by Pure...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi AMP'D UP Advanced Weight Loss Dietary Supplement capsules Recalled...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi BTrim ULTIMATE BOOST Dietary Supplement capsules Recalled by Pure...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi BTrim MAX Dietary Supplement capsules Recalled by Pure Edge...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi INSANE Bee Pollen Dietary Supplement Capsules Recalled by Pure Edge...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugOctober 10, 2013· Pure Edge Nutrition

Recalled Item: Bella Vi INSANE AMP'D Dietary Supplement capsules Recalled by Pure Edge...

The Issue: Marketed without an Approved NDA/ANDA; product was found to contain...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
FoodOctober 10, 2013· Nutrition Center, Inc. dba Nutri-West

Recalled Item: Total Enzyme Recalled by Nutrition Center, Inc. dba Nutri-West Due to...

The Issue: Nutrition Center voluntarily recalled Total Enzymes and Total Probiotics...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodOctober 10, 2013· Nutrition Center, Inc. dba Nutri-West

Recalled Item: Total Probiotics Recalled by Nutrition Center, Inc. dba Nutri-West Due to...

The Issue: Nutrition Center voluntarily recalled Total Enzymes and Total Probiotics...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 10, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: VariAx Compression Plating System Recalled by Stryker Howmedica Osteonics...

The Issue: Stryker received two reports indicating that during screw insertion under a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Mixing Cup Arrays utilized on VITROS 250 Recalled...

The Issue: Ortho Clinical Diagnostics issued a product correction notification for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Nova Biomedical Corporation

Recalled Item: Nova StatStrip/StatSensor Hospital Blood Glucose Meter Recalled by Nova...

The Issue: Revised Battery Instructions for Removal and Expiration Date due to battery...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2013· Mizuho America, Inc.

Recalled Item: Mizuho Sugita Titanium Standard Aneurysm Clip II Recalled by Mizuho America,...

The Issue: Specific item numbers form Lots 27-J and 29-J of Sugita T2 Aneurysm Clips....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing