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. 2,394 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,394 in last 12 months

Showing 4192141940 of 49,744 recalls

Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens syngo RT Dosimetrist 2.7 system Product Usage: The intended Recalled...

The Issue: An update to the Virtual Simulation software of the syngo RT Dosimetrist is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Synthes, Inc.

Recalled Item: Synthes B37 Replacement Screws. M3.5 Screw for insertion handle guide/aiming...

The Issue: All lots of B37 Replacement Screws are being recalled due to potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Focus Diagnostics Inc

Recalled Item: Simplexa" Flu A/B & RSV Direct Recalled by Focus Diagnostics Inc Due to...

The Issue: Focus Diagnostics is providing an urgent safety notice for a correction to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Biomet, Inc.

Recalled Item: DISCOVERY ELBOW prosthesis Recalled by Biomet, Inc. Due to Surface finish is...

The Issue: Surface finish is different than specified. The implant has 30 grit blast on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips MR systems: Trolley Variable Height IRF (for Ingenia 1.5T Recalled...

The Issue: Ingenia customers have experienced clamping of the foot under the central...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Ebi, Llc

Recalled Item: Biomet Spine Recalled by Ebi, Llc Due to The Cypher MIS Screw Inserter may...

The Issue: The Cypher MIS Screw Inserter may exhibit an increased rate of instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips MR systems: Ingenia HA FLEX TRAK Trolley (for Ingenia Recalled by...

The Issue: Ingenia customers have experienced clamping of the foot under the central...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2014· Boston Scientific Corporation

Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...

The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...

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

Class II — Potential Health HazardOngoing
DrugMay 14, 2014· Oasis Medical Inc

Recalled Item: Oasis TEARS Recalled by Oasis Medical Inc Due to Labeling: Missing Label;...

The Issue: Labeling: Missing Label; The label on the immediate bottle is missing.

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

Class III — Low RiskOngoing
Refund
FoodMay 14, 2014· Diamond Crystal Brands, Inc.

Recalled Item: Poco Pac Salad Dressing Recalled by Diamond Crystal Brands, Inc. Due to...

The Issue: Undeclared Allergen: Egg

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 14, 2014· Beckman Coulter, Inc.

Recalled Item: MicroScan -Neg Breakpoint Combo Panel Type 34 Recalled by Beckman Coulter,...

The Issue: Siemens Healthcare Diagnostics has received complaints regarding panel...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 14, 2014· NxStage Medical, Inc.

Recalled Item: NxStage Dialysate Sack (SAK) with Concentrate for Use with PureFlow Recalled...

The Issue: SAK Dialysate Concentrate contain aluminum levels which exceed internal...

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

Class II — Potential Health HazardOngoing