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. 2,548 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,548 in last 12 months

Showing 1846118480 of 49,744 recalls

DrugApril 20, 2020· Glaxosmithkline Consumer Healthcare Holdings

Recalled Item: ChapStick Total Hydration Moisture + Tint + SPF15 Very Berry Recalled by...

The Issue: Labeling: Not elsewhere classified: Observed separation in the secondary...

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

Class III — Low RiskOngoing
Refund
DrugApril 20, 2020· Glaxosmithkline Consumer Healthcare Holdings

Recalled Item: ChapStick Total Hydration Moisture + Tint + SPF15 Pretty in Recalled by...

The Issue: Labeling: Not elsewhere classified: Observed separation in the secondary...

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

Class III — Low RiskOngoing
Refund
DrugApril 20, 2020· Glaxosmithkline Consumer Healthcare Holdings

Recalled Item: ChapStick Total Hydration Moisture + Tint + SPF15 Peachy Keen Recalled by...

The Issue: Labeling: Not elsewhere classified: Observed separation in the secondary...

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

Class III — Low RiskOngoing
Refund
DrugApril 20, 2020· Lupin Pharmaceuticals Inc.

Recalled Item: Lisinopril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to Product...

The Issue: Product Mix-Up: a complaint received indicating mix-up of 10 mg Lisinopril...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 20, 2020· Suntech Medical, Inc.

Recalled Item: Oscar 2 Recalled by Suntech Medical, Inc. Due to The device display, when...

The Issue: The device display, when activated, can show an incorrect decimal point when...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· ROi CPS LLC

Recalled Item: Regard. Item number: 830034. GS0348D- CVC Triple Lumen 20CM non Sulfa-Mercy....

The Issue: Custom procedure kits contains affected lots of PosiFlush Syringe, a product...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Trividia Health, Inc.

Recalled Item: TRUE METRIX SELF MONITORING BLOOD GLUCOSE SYSTEM - Product Usage: Recalled...

The Issue: One (1) TRUE METRIX AIR blood glucose meter distributed in the United States...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Philips North America, LLC

Recalled Item: Philips Sterilizable Defibrillator Internal Paddles - Internal paddles are...

The Issue: Internal Paddles may wear over time and may not be safe or ready for use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Bovie Medical Corporation

Recalled Item: Renuvion/ J-Plasma Precise Handpiece. Catalog numbers BVX-150B Recalled by...

The Issue: Unexpected stress fractures on the shaft of the hand piece may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Cardinal Health Inc.

Recalled Item: Professional Urine Drug Control Recalled by Cardinal Health Inc. Due to...

The Issue: Three products requiring storage conditions were incorrectly stored outside...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Bovie Medical Corporation

Recalled Item: Renuvion/ J-Plasma Precise Open Handpiece. Catalog numbers BVX-044-BPS...

The Issue: Unexpected stress fractures on the shaft of the hand piece may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Cardinal Health Inc.

Recalled Item: B-Hydroxybutyrate LiquiColor Recalled by Cardinal Health Inc. Due to Three...

The Issue: Three products requiring storage conditions were incorrectly stored outside...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Cardinal Health Inc.

Recalled Item: Strep B Carrot Broth One-Step Recalled by Cardinal Health Inc. Due to Three...

The Issue: Three products requiring storage conditions were incorrectly stored outside...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Cios Alpha VA30-mobile X-Ray system Recalled by Siemens Medical...

The Issue: Main cable can be plugged or unplugged from the X10 connector which is part...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Cios Alpha VA20-mobile X-Ray system Material # 10308191 The Recalled...

The Issue: Main cable can be plugged or unplugged from the X10 connector which is part...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Cios Spin VA30-mobile X-Ray system Recalled by Siemens Medical...

The Issue: Main cable can be plugged or unplugged from the X10 connector which is part...

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

Class II — Potential Health HazardOngoing
DrugApril 18, 2020· B. Braun Medical Inc

Recalled Item: Ceftazidime for Injection USP and Dextrose for Injection USP Recalled by B....

The Issue: Failed Stability Specifications: Out-of-Specification (OOS) results for High...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 17, 2020· Alcon Research LLC

Recalled Item: Acrysof Recalled by Alcon Research LLC Due to Incorrect IOL diopter

The Issue: Incorrect IOL diopter

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2020· Baxter Healthcare Corporation

Recalled Item: Gambro Cartridge Low Weight-Low Volume Blood Transport System for...

The Issue: Potential disconnection of tubing set.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2020· Baxter Healthcare Corporation

Recalled Item: Gambro Cartridge Blood Set Prime Line - Product Usage: is Recalled by Baxter...

The Issue: Potential disconnection of tubing set.

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

Class II — Potential Health HazardOngoing