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 4378143800 of 49,744 recalls

Medical DeviceOctober 25, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: 1) Accolade II 127 Neck Angle Hip Stem Recalled by Stryker Howmedica...

The Issue: Stryker received a report from the field indicating that an Accolade II Hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2013· Biomet, Inc.

Recalled Item: Security (TM) Enclosed Carpal Tunnel System Blade ( Recalled by Biomet, Inc....

The Issue: Security Blades were manufactured oversized and potentially won't advance or...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2013· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Aviva Combo Blood Glucose Meter (as a part of Recalled by Roche...

The Issue: There is a software synchronization issue with the ACCU-CHEK Combo system....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Discovery NMCT 670 Recalled by GE Healthcare, LLC Due to GE...

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

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

Class II — Potential Health HazardOngoing
DrugOctober 24, 2013· Teva Pharmaceuticals USA

Recalled Item: Copaxone (glatiramer acetate injection) Recalled by Teva Pharmaceuticals USA...

The Issue: Presence of Particulate Matter: A foreign particle found in a pre-filled...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 24, 2013· Irwin Naturals

Recalled Item: Dual Action Cleanse by Cellular Research Formulas Recalled by Irwin Naturals...

The Issue: Irwin Naturals is recalling Daily Digestive Enzymes and Dual Action Cleanse...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 24, 2013· Irwin Naturals

Recalled Item: Irwin Naturals Daily Digestive Enzymes 45 ct Recalled by Irwin Naturals Due...

The Issue: Irwin Naturals is recalling Daily Digestive Enzymes and Dual Action Cleanse...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 24, 2013· Irwin Naturals

Recalled Item: Dual Action Cleanse by Cellular Research Formulas with Green Tea Bonus 60 ct...

The Issue: Irwin Naturals is recalling Daily Digestive Enzymes and Dual Action Cleanse...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 24, 2013· Kimberly-Clark Corporation

Recalled Item: Kimberly-Clark Single Shot Epidural Pain Management Trays containing the BD...

The Issue: Kimberly-Clark Single Shot Epidural Pain Management Trays contain the BD 7...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2013· Varian Medical Systems, Inc.

Recalled Item: C-Series: Clinac Recalled by Varian Medical Systems, Inc. Due to This...

The Issue: This correction is to notify users that a solution to a previous correction...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 24, 2013· Nobel Biocare Usa Llc

Recalled Item: Osseocare Pro Console & Set Osseocare Pro Recalled by Nobel Biocare Usa Llc...

The Issue: The recall was initiated because there is a potential for malfunction of the...

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

Class II — Potential Health HazardOngoing
FoodOctober 23, 2013· New Algae Company

Recalled Item: Flex Recalled by New Algae Company Due to Flex dietary supplement product is...

The Issue: Flex dietary supplement product is recalled because the finished label does...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 23, 2013· New Algae Company

Recalled Item: EDGE Recalled by New Algae Company Due to EDGE dietary supplement product is...

The Issue: EDGE dietary supplement product is recalled because the finished label does...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 23, 2013· Philips Medical Systems, Inc.

Recalled Item: BrightView XCT is a gamma camera for Single Photon Emission Recalled by...

The Issue: It was discovered the CT portion of the scan was interrupted ( stopping the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS brand ARTISTE Linear Accelerator Linac systems with component: any...

The Issue: A safety risk regarding a potentially existing dark current radiation...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS brand ONCOR series Linear Accelerator Linac systems with component:...

The Issue: A safety risk regarding a potentially existing dark current radiation...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Alere San Diego, Inc.

Recalled Item: Product Brand Name(s): Alere Cholestech LDX¿ Lipid Profile"GLU Test Cassette...

The Issue: Alere initiated a recall of Cholestech LDX Lipid Profile-GLU test cassettes,...

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

Class III — Low RiskOngoing
Medical DeviceOctober 23, 2013· ConMed Corporation

Recalled Item: ALTRUS¿ THERMAL TISSUE FUSION Recalled by ConMed Corporation Due to The...

The Issue: The affected lots were exposed to a higher than acceptable level of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Carl Zeiss Meditec, Inc.

Recalled Item: Zeiss brand IOLMaster 500 Recalled by Carl Zeiss Meditec, Inc. Due to The...

The Issue: The user database delivered for download contained an erroneous value....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2013· Carl Zeiss Meditec, Inc.

Recalled Item: Zeiss brand IOLMaster Recalled by Carl Zeiss Meditec, Inc. Due to The user...

The Issue: The user database delivered for download contained an erroneous value....

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

Class II — Potential Health HazardOngoing