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 32213240 of 49,744 recalls

Medical DeviceJanuary 28, 2025· GE Medical Systems, LLC

Recalled Item: Definium 656HD & Discovery XR656HD (GTINs: 00840682138598 Recalled by GE...

The Issue: The user can continue to take the next exposure after reaching the Automatic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2025· GE Medical Systems, LLC

Recalled Item: Discovery XR656 HD. X-Ray imaging system. Recalled by GE Medical Systems,...

The Issue: The user can continue to take the next exposure after reaching the Automatic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 28, 2025· GE Medical Systems, LLC

Recalled Item: Discovery XR656HD. X-Ray imaging system. Recalled by GE Medical Systems, LLC...

The Issue: The user can continue to take the next exposure after reaching the Automatic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Hiossen Inc.

Recalled Item: ET Rigid Abutment (Mini) SIze: 4.5D 4.0G/H 4.0H - Intended Recalled by...

The Issue: Patient chart stickers provided inside the packaging may incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Hiossen Inc.

Recalled Item: Osstem Implant System - Abutment ET Multi Abutment Size: 4.8D Recalled by...

The Issue: Patient chart stickers provided inside the packaging may incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Hiossen Inc.

Recalled Item: ET Rigid Abutment (Mini) Size 4.5D 1.0G/H 5.0H - Intended Recalled by...

The Issue: Patient chart stickers provided inside the packaging may incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Hiossen Inc.

Recalled Item: ET Rigid Abutment (Mini) SIze: 4.5D 3.0G/H 7.0H - Intended Recalled by...

The Issue: Patient chart stickers provided inside the packaging may incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Hiossen Inc.

Recalled Item: ET Rigid Abutment (Mini) Size: 4.5D 2.0G/H 4.0H- Intended for Recalled by...

The Issue: Patient chart stickers provided inside the packaging may incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· TAS Medical Inc

Recalled Item: TISSUE APPROXIMATION SYSTEM (TAS) Recalled by TAS Medical Inc Due to Tissue...

The Issue: Tissue approximation straps (zip-ties) have broken before or during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Hiossen Inc.

Recalled Item: Osstem Implant System - Abutment: ET Multi AbutmentSize: 4.8D 5.0GH Recalled...

The Issue: Patient chart stickers provided inside the packaging may incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Dexcom, Inc.

Recalled Item: Dexcom G6 Recalled by Dexcom, Inc. Due to Under very rare situations, the...

The Issue: Under very rare situations, the Dexcom G6 touchscreen receiver may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Dexcom, Inc.

Recalled Item: Dexcom G6 Recalled by Dexcom, Inc. Due to Under very rare situations, the...

The Issue: Under very rare situations, the Dexcom G6 touchscreen receiver may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 27, 2025· Dexcom, Inc.

Recalled Item: Dexcom G6 Recalled by Dexcom, Inc. Due to Under very rare situations, the...

The Issue: Under very rare situations, the Dexcom G6 touchscreen receiver may not...

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

Class II — Potential Health HazardOngoing
FoodJanuary 25, 2025· Amazon Retail LLC

Recalled Item: ASIN B0CY2RDW5T Recalled by Amazon Retail LLC Due to Undeclared Egg

The Issue: Undeclared egg.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 25, 2025· Amazon Retail LLC

Recalled Item: ASIN B084PZ7K98 Recalled by Amazon Retail LLC Due to Undeclared Egg

The Issue: Undeclared egg.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2025· SKY PACKAGING

Recalled Item: HydrALAZINE Hydrochloride Recalled by SKY PACKAGING Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 24, 2025· SKY PACKAGING

Recalled Item: HydrALAZINE Hydrochloride Recalled by SKY PACKAGING Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 24, 2025· Guangzhou Pluslife Biotech Co., Ltd.

Recalled Item: Brand Name: Pluslife SARS-CoV-2 Card Product Name: SARS-CoV-2 Nucleic Acid...

The Issue: Devices were distributed in the U.S. market without obtaining the required...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2025· Guangzhou Pluslife Biotech Co., Ltd.

Recalled Item: Brand Name: MiniDock Product Name: Integrated Nucleic Acid Testing Device...

The Issue: Devices were distributed in the U.S. market without obtaining the required...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2025· CareFusion 303, Inc.

Recalled Item: BD Alaris Pump Module The BD Alaris System Recalled by CareFusion 303, Inc....

The Issue: Due to User Manual/Direction for Use incorrectly instructing user to leave...

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

Class II — Potential Health HazardOngoing