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. 2,661 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,661 in last 12 months

Showing 14811500 of 28,172 recalls

Medical DeviceJune 11, 2025· CooperSurgical, Inc.

Recalled Item: Endosee System Convenience Kit with IV Tube. Model Number: ES-TRAY-IV....

The Issue: The HSG Procedure Trays and Endosee System Convenience Kits contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· CooperSurgical, Inc.

Recalled Item: Endosee System Convenience Kit. Model Number: ES-TRAY. Endosee System...

The Issue: The HSG Procedure Trays and Endosee System Convenience Kits contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· CooperSurgical, Inc.

Recalled Item: HSG Procedure Tray. Model Number: 6050T. The HSG Procedure Tray Recalled by...

The Issue: The HSG Procedure Trays and Endosee System Convenience Kits contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 11, 2025· RECORDATI RARE DISEASES INC.

Recalled Item: Caphosol Artificial Saliva (32 doses sachet box). 64 x 15 Recalled by...

The Issue: Out of specification stability test result for the Caphosol B solution from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Foundation For Sight

Recalled Item: BostonSight SCLERAL Lens Recalled by Boston Foundation For Sight Due to...

The Issue: Select orders of lenses were manufactured with errors impacting sagittal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Foundation For Sight

Recalled Item: BostonSight PROSE Lens. Recalled by Boston Foundation For Sight Due to...

The Issue: Select orders of lenses were manufactured with errors impacting sagittal...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry...

The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry...

The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products CHE Slides Recalled by Ortho-Clinical Diagnostics,...

The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products CHE Slides (Japan) Recalled by Ortho-Clinical...

The Issue: Quality control (QC) drift when certain lots of Performance Verifiers (PVs)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Scientific Corporation

Recalled Item: Torflex Transseptal Guiding Sheath Kit (TFK-M) TF85-32-63-45 TORFLEX 8.5F...

The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Scientific Corporation

Recalled Item: VersaCross Access Solution (VXSK) Recalled by Boston Scientific Corporation...

The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Scientific Corporation

Recalled Item: VersaCross RF Wire (VXW). Indicated for creation of an atrial Recalled by...

The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2025· Boston Scientific Corporation

Recalled Item: VersaCross Transseptal Sheath Kit (VXS) Product Description/IDs VXS0201 VXS...

The Issue: Potential for hole in the Tyvek layer of the sterile barrier pouch, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2025· Boston Scientific Neuromodulation Corporation

Recalled Item: Superion IDS Kit Superion Indirect Decompression System 8MM Recalled by...

The Issue: As a result of a comprehensive product performance review it was determine...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2025· Merit Medical Systems, Inc.

Recalled Item: Custom Manifold Kit: Recalled by Merit Medical Systems, Inc. Due to High...

The Issue: High pressure tubing may relax over time causing it to partially separate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2025· Merit Medical Systems, Inc.

Recalled Item: Custom Tubing Kit: Recalled by Merit Medical Systems, Inc. Due to High...

The Issue: High pressure tubing may relax over time causing it to partially separate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2025· Merit Medical Systems, Inc.

Recalled Item: High Pressure Tubing: Recalled by Merit Medical Systems, Inc. Due to High...

The Issue: High pressure tubing may relax over time causing it to partially separate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2025· Merit Medical Systems, Inc.

Recalled Item: Custom Waste Management Kit: Recalled by Merit Medical Systems, Inc. Due to...

The Issue: High pressure tubing may relax over time causing it to partially separate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2025· Waismed Ltd.

Recalled Item: Brand Name: NIO+ Product Name: NIO Intraosseous Device Adult Model/Catalog...

The Issue: Due to manufacturing error, Intraosseous device built-in stabilizer may not...

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

Class II — Potential Health HazardOngoing