Product Recalls in Mississippi

Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,372 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,372 in last 12 months

Showing 4412144140 of 49,744 recalls

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
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
Medical DeviceOctober 10, 2013· Biomet, Inc.

Recalled Item: Juggerknotless Drill Bit Recalled by Biomet, Inc. Due to Investigation...

The Issue: Investigation identified that the design of the drill bit may make the...

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

Class II — Potential Health HazardOngoing
DrugOctober 9, 2013· Actavis Elizabeth LLC

Recalled Item: Alprazolam Orally Disintegrating Tablets Recalled by Actavis Elizabeth LLC...

The Issue: Failed Tablet/Capsule Specifications; partial tablet erosion resulting in...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2013· Sandoz, Inc

Recalled Item: Ropinirole Recalled by Sandoz, Inc Due to Cross contamination with other...

The Issue: Cross contamination with other products: Sandoz is recalling certain lots of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 9, 2013· GE Healthcare, LLC

Recalled Item: GE Optima CT520 and Optima CT540 Computed Tomography (CT) systems. Recalled...

The Issue: There is an issue with the Manual Film Composer feature on some CT products....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2013· Arrow International Inc

Recalled Item: Continuous Peripheral Nerve Block Catheter Kit and Set Continuous Peripheral...

The Issue: A labeling inconsistency was discovered in which the lidstock states that...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 9, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS CA 125 II Calibrators For use in the calibration Recalled by...

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 9, 2013· Arrow International Inc

Recalled Item: Arrow Transradial Artery Access products Arrow Transradial Artery Access...

The Issue: There is a risk that the introducer needles packaged within the kits can be...

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

Class II — Potential Health HazardOngoing