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 21012120 of 49,744 recalls

DrugJune 27, 2025· Sandoz Inc

Recalled Item: Cefazolin for Injection Recalled by Sandoz Inc Due to Labeling: Label...

The Issue: Labeling: Label Mix-Up; cartons of Cefazolin for Injection, USP 1 gram were...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 27, 2025· Sandoz Inc

Recalled Item: Buffered Penicillin G Potassium for Injection Recalled by Sandoz Inc Due to...

The Issue: Labeling: Label Mix-Up; Some vials of Cefazolin for Injection, USP 1 gram...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 27, 2025· Maquet Cardiopulmonary Gmbh

Recalled Item: Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold...

The Issue: Device does not comply with the labeling requirements of international...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2025· Microbiologics Inc

Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to KWIK-STIK : 0894P, 0894K and...

The Issue: KWIK-STIK : 0894P, 0894K and LYFO DISK" 0894L may result in failure to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2025· Spiggle & Theis Mt Gmbh

Recalled Item: Injection needle Recalled by Spiggle & Theis Mt Gmbh Due to Affected product...

The Issue: Affected product show elevated cytotoxicity values. Use of affected...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2025· Microbiologics Inc

Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to KWIK-STIK : 0894P, 0894K and...

The Issue: KWIK-STIK : 0894P, 0894K and LYFO DISK" 0894L may result in failure to...

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

Class II — Potential Health HazardOngoing
DrugJune 26, 2025· AvKARE

Recalled Item: Pitavastatin Tablets Recalled by AvKARE Due to Failed Impurity/Degradation...

The Issue: Failed Impurity/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugJune 26, 2025· AvKARE

Recalled Item: Pitavastatin Tablets Recalled by AvKARE Due to Failed Impurity/Degradation...

The Issue: Failed Impurity/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 26, 2025· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPoint 500 Systems Wash/Waste Cartridge (4 Pack). Material Number:...

The Issue: Siemens Healthcare Diagnostics is recalling the RAPIDPoint 500 Systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2025· Hamilton Medical AG

Recalled Item: Breathing circuit set Recalled by Hamilton Medical AG Due to Ventilator...

The Issue: Ventilator coaxial breathing circuit may have a crack in blue tubing, which...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 25, 2025· Preat Corp

Recalled Item: NobelBiocare Tri-Lobe-compatible WP X 6.0mm Engaging Titanium Base Recalled...

The Issue: Engaging titanium base was manufactured 180 degrees around the post from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2025· Boston Scientific Corporation

Recalled Item: FARAWAVE 1.0 Pulsed Field Ablation Catheter Recalled by Boston Scientific...

The Issue: The potentially impacted units were manufactured using specific equipment...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2025· Beckman Coulter, Inc.

Recalled Item: DxI 800 Access Immunoassay Analyzer W/Dual Gantry Recalled by Beckman...

The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2025· Beckman Coulter, Inc.

Recalled Item: DxI 600 Access Immunoassay Analyzer W/Spot B Recalled by Beckman Coulter,...

The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2025· Beckman Coulter, Inc.

Recalled Item: DxI 800 Access Immunoassay Analyzer W/Spot B Recalled by Beckman Coulter,...

The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2025· Beckman Coulter, Inc.

Recalled Item: DxI 600 Access Immunoassay Analyzer W/Dual Gantry Recalled by Beckman...

The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2025· Beckman Coulter, Inc.

Recalled Item: UniCel DxI 600 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc....

The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2025· Beckman Coulter, Inc.

Recalled Item: UniCel DxI 800 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc....

The Issue: Beckman Coulter has identified that the UniCel DxI 600/800 systems with...

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

Class II — Potential Health HazardOngoing
FoodJune 24, 2025· Enjoy Nutrition, LLC; dba Weyland Brain Nutrition

Recalled Item: Lithium Orotate Recalled by Enjoy Nutrition, LLC; dba Weyland Brain...

The Issue: Under potency / misbranding: product fails to meet labeled lithium orotate...

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

Class III — Low RiskOngoing
Refund
FoodJune 24, 2025· Enjoy Nutrition, LLC; dba Weyland Brain Nutrition

Recalled Item: Lithium Orotate Recalled by Enjoy Nutrition, LLC; dba Weyland Brain...

The Issue: Under potency / misbranding: product fails to meet labeled lithium orotate...

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

Class III — Low RiskOngoing
Refund