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. 2,429 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,429 in last 12 months

Showing 3606136080 of 49,744 recalls

DrugSeptember 10, 2015· EMD Serono, Inc.

Recalled Item: ClomiPHENE CITRATE Tablets Recalled by EMD Serono, Inc. Due to Chemical...

The Issue: Chemical Contamination: impurity failure due to chemical contamination of...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 10, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software Anomaly...

The Issue: Software Anomaly during ADD Installation on VITROS 5,1 FS Chemistry Systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2015· Smith & Nephew, Inc., Endoscopy Div.

Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 3.5 mm Recalled...

The Issue: Sterility of device is compromised due to breach in the packaging

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2015· Smith & Nephew, Inc., Endoscopy Div.

Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 4.5 mm Recalled...

The Issue: Sterility of device is compromised due to breach in the packaging

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2015· Smith & Nephew, Inc., Endoscopy Div.

Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 6.5 mm Recalled...

The Issue: Sterility of device is compromised due to breach in the packaging

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2015· Smith & Nephew, Inc., Endoscopy Div.

Recalled Item: Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 8.5 mm Recalled...

The Issue: Sterility of device is compromised due to breach in the packaging

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2015· Beckman Coulter Inc.

Recalled Item: MICroSTREP plus 1 Panel Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is recalling MICroSTREP plus 1 and MICroSTREP plus 2 panels...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2015· Beckman Coulter Inc.

Recalled Item: MICroSTREP plus 2 Panel Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is recalling MICroSTREP plus 1 and MICroSTREP plus 2 panels...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2015· Biosense Webster, Inc.

Recalled Item: SOUNDSTAR eco 8F and 10F Diagnostic Ultrasound Catheters. For intra-cardiac...

The Issue: Image disappeared from the cardiac ultrasound system when the CARTO 3 EP...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2015· Biosense Webster, Inc.

Recalled Item: Carto 3 EP Navigation System. Electro physiology system which views Recalled...

The Issue: Image disappeared from the cardiac ultrasound system when the CARTO 3 EP...

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

Class II — Potential Health HazardOngoing
DrugSeptember 9, 2015· Ferring Pharmaceuticals Inc

Recalled Item: Bravelle 75 IU (urofollitropin for injection Recalled by Ferring...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 9, 2015· Abbott Laboratories, Inc

Recalled Item: ARCHITECT i2000SR System The Abbott ARCHITECT System is intended for...

The Issue: Incorrect tubing.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2015· Intuitive Surgical, Inc.

Recalled Item: Fluorescence Imaging Procedure Kits used with the da Vinci Si Recalled by...

The Issue: B. Braun 2 gang 4-way stopcocks in the Fluorescence Imaging Procedure Kit...

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

Class II — Potential Health HazardOngoing
FoodSeptember 8, 2015· Family Dollar Stores - NC Distribution Center

Recalled Item: Family Gourmet Long Grain Enriched White Rice Recalled by Family Dollar...

The Issue: Live insects were noted inside several unopened bags of product.

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 8, 2015· Family Dollar Stores - NC Distribution Center

Recalled Item: Family Gourmet Natural Whole Grain Brown Rice Recalled by Family Dollar...

The Issue: Live insects were noted inside several unopened bags of product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 8, 2015· ErgoSafe Products, LLC (DBA) Prism Medical

Recalled Item: Prism Medical P-300 Portable Consumer Lift Recalled by ErgoSafe Products,...

The Issue: Drive shaft and over speed arm may simultaneously fail potentially resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2015· ErgoSafe Products, LLC (DBA) Prism Medical

Recalled Item: Prism Medical C-300 Consumer Ceiling Lift Recalled by ErgoSafe Products, LLC...

The Issue: Drive shaft and over speed arm may simultaneously fail potentially resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2015· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Orthopaedics Tapers LFIT V40 Vitallium femoral heads. hip prosthesis...

The Issue: Complaints that the femoral head could not be assembled with its...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2015· Stryker Spine

Recalled Item: Stryker UniVise Spinous Process Fixation Plate System Inserter Recalled by...

The Issue: The Inserter Inner Shaft would not fit through the Inserter. The inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2015· DePuy Orthopaedics, Inc.

Recalled Item: Specialist 2 Intramedullary (SP2 IM) Rod 400mm Instrument (PN 96-6120)...

The Issue: DePuy Orthopaedics, Inc. is initiating a voluntary recall of select lots of...

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

Class II — Potential Health HazardOngoing