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. 2,645 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,645 in last 12 months

Showing 39413960 of 49,744 recalls

Medical DeviceOctober 28, 2024· GE Medical Systems, LLC

Recalled Item: SIGNA Architect AIR Recalled by GE Medical Systems, LLC Due to Gradient...

The Issue: Gradient coils for certain MR systems (see affected product list in this...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2024· GE Medical Systems, LLC

Recalled Item: Discovery MR750w 3.0T Recalled by GE Medical Systems, LLC Due to Gradient...

The Issue: Gradient coils for certain MR systems (see affected product list in this...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2024· GE Medical Systems, LLC

Recalled Item: SIGNA Architect Recalled by GE Medical Systems, LLC Due to Gradient coils...

The Issue: Gradient coils for certain MR systems (see affected product list in this...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2024· GE Medical Systems, LLC

Recalled Item: Tomographic Imager Combining Emission Computed Tomography With Nuclear...

The Issue: Gradient coils for certain MR systems (see affected product list in this...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2024· Remote Diagnostic Technologies Ltd.

Recalled Item: Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a...

The Issue: Due to incorrect labels applied to devices during servicing. Labels contain...

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

Class III — Low RiskOngoing
DrugOctober 25, 2024· Lannett Company Inc.

Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by Lannett Company Inc. Due to...

The Issue: Failed Content Uniformity Specifications: Product failed to meet the action...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 25, 2024· Noah Medical

Recalled Item: Galaxy bronchoscope (Product GALB-001) used with Instructions for use...

The Issue: Not all biopsy tools meant to fit bronchoscope channel (2.1mm inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 25, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: ENDO KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Identified...

The Issue: Identified lots of Olympus product may be missing sterile and manufacturing...

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

Class II — Potential Health HazardOngoing
DrugOctober 24, 2024· Unexo Life Sciences Private Limited

Recalled Item: THERACARE Cold Hot Medicated Patch Recalled by Unexo Life Sciences Private...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2024· Unexo Life Sciences Private Limited

Recalled Item: ABSORBINE jr. Extra Large BACK PATCH Recalled by Unexo Life Sciences Private...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2024· Unexo Life Sciences Private Limited

Recalled Item: PARCHE LEON PAIN RELIEVING HOT PATCH Recalled by Unexo Life Sciences Private...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2024· Unexo Life Sciences Private Limited

Recalled Item: THERACARE MAXIMUM STRENGTH PAIN RELIEF 4% LIDOCAINE PATCH Recalled by Unexo...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2024· Unexo Life Sciences Private Limited

Recalled Item: LILAS Feminine Pain Relief Patch Recalled by Unexo Life Sciences Private...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2024· Unexo Life Sciences Private Limited

Recalled Item: EQUATE MAXIMUM STRENGTH LIDOCAINE PAIN RELIEVING PATCH Lidocaine 4% Topical...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2024· Unexo Life Sciences Private Limited

Recalled Item: JR WATKINS COOLING PAIN RELIEF PATCHES Recalled by Unexo Life Sciences...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2024· Unexo Life Sciences Private Limited

Recalled Item: ABSORBINE jr ULTRA STRENGTH PAIN PATCH Recalled by Unexo Life Sciences...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2024· Unexo Life Sciences Private Limited

Recalled Item: CHEEKY BONSAI PAIN RELIEF PATCHES Recalled by Unexo Life Sciences Private...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2024· Unexo Life Sciences Private Limited

Recalled Item: ABSORBINE JR PAIN RELIEVING KNEE PATCH Recalled by Unexo Life Sciences...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2024· Unexo Life Sciences Private Limited

Recalled Item: HealthWise PERIOD PATCH Menstrual Pain Relief Recalled by Unexo Life...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 24, 2024· GE Healthcare (China) Co., Ltd.

Recalled Item: GE Proteus XR/A radiographic system Recalled by GE Healthcare (China) Co.,...

The Issue: Steel cables in the Wall Stand for certain Proteus XR/a systems serviced by...

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

Class II — Potential Health HazardOngoing