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 36413660 of 49,744 recalls

DrugDecember 2, 2024· RemedyRepack Inc.

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by RemedyRepack Inc. Due to...

The Issue: CGMP Deviations; presence of N-nitroso-duloxetine impurity above recommended...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 2, 2024· Coloplast Manufacturing US, LLC

Recalled Item: X-Flow prostatectomy catheter Recalled by Coloplast Manufacturing US, LLC...

The Issue: A possible sterility issue was detected in Coloplast's facility on some...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· A L I Technologies Ltd

Recalled Item: Change Healthcare Cardiology Hemo software Recalled by A L I Technologies...

The Issue: Software defect concerning autosave mechanism may result in the clinician...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· Accriva Diagnostics, Inc.

Recalled Item: VerifyNow P2Y12 Platelet Reactivity Test Recalled by Accriva Diagnostics,...

The Issue: Platelet Reactivity Test distributed without appropriate US-FDA market...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· A L I Technologies Ltd

Recalled Item: McKesson Cardiology Hemo software Recalled by A L I Technologies Ltd Due to...

The Issue: Software defect concerning autosave mechanism may result in the clinician...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· A L I Technologies Ltd

Recalled Item: Change Healthcare Cardiology Hemodynamics software Recalled by A L I...

The Issue: Software defect concerning autosave mechanism may result in the clinician...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· Coloplast Manufacturing US, LLC

Recalled Item: Folysil Silicone Foley Catheters Recalled by Coloplast Manufacturing US, LLC...

The Issue: A possible sterility issue was detected in Coloplast's facility on some...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2024· Moximed, Inc.

Recalled Item: MISHA Knee System Implant Small Recalled by Moximed, Inc. Due to Knee...

The Issue: Knee implant may fracture due to a supplier-related issue with one component...

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

Class II — Potential Health HazardOngoing
FoodNovember 29, 2024· Terry and Joe Baker Farms, LLC dba Baker Farms

Recalled Item: Baker Farms CURLY MUSTARD 16 oz NET WT 16 oz Recalled by Terry and Joe Baker...

The Issue: The firm was notified by the Texas Department of Agriculture that the...

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 27, 2024· Bazzini LLC

Recalled Item: NuGo Dark Chocolate Pretzel with Sea Salt Recalled by Bazzini LLC Due to...

The Issue: The product is being recalled because of undeclared milk .

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 27, 2024· Bazzini LLC

Recalled Item: NuGo Dark Pretzel/Chocolate Chip Multipack 18 ct. Recalled by Bazzini LLC...

The Issue: The product is being recalled because of undeclared milk .

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

Class I — Serious Health HazardOngoing
Refund
FoodNovember 27, 2024· Bazzini LLC

Recalled Item: NuGo Dark Chocolate Chip Recalled by Bazzini LLC Due to Undeclared Milk

The Issue: The product is being recalled because of undeclared milk .

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 27, 2024· AvKARE

Recalled Item: Cinacalcet Tablets Recalled by AvKARE Due to CGMP deviations: Presence of...

The Issue: CGMP deviations: Presence of Nitrosamine Drug Substance Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 27, 2024· AvKARE

Recalled Item: Cinacalcet Tablets Recalled by AvKARE Due to CGMP deviations: Presence of...

The Issue: CGMP deviations: Presence of Nitrosamine Drug Substance Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 27, 2024· AvKARE

Recalled Item: Cinacalcet Tablets Recalled by AvKARE Due to CGMP deviations: Presence of...

The Issue: CGMP deviations: Presence of Nitrosamine Drug Substance Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 27, 2024· IsoTis OrthoBiologics, Inc.

Recalled Item: OsteoSurge 100 Demineralized Bone Matrix Putty with Accell Bone Matrix...

The Issue: Incorrect expiration date listed on the outer box, which does not align with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2024· IsoTis OrthoBiologics, Inc.

Recalled Item: OsteoCove Putty Recalled by IsoTis OrthoBiologics, Inc. Due to Hydration...

The Issue: Hydration issue resulting in the product being less cohesive and moldable...

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

Class II — Potential Health HazardOngoing
DrugNovember 26, 2024· Curium US, LLC

Recalled Item: Kit for the Preparation of Technetium Tc 99m Sestamibi Injection Recalled by...

The Issue: Lack of Assurance of Sterility; Improper crimps on vials impacting the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 26, 2024· O&M HALYARD, INC.

Recalled Item: Brand Name: HALYARD Product Name: Laparotomy Pack Model/Catalog Number:...

The Issue: Elevated residues of anti-block/slip additive used in manufacturing found...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2024· Beckman Coulter, Inc.

Recalled Item: Access Intact PTH assay Recalled by Beckman Coulter, Inc. Due to Beckman...

The Issue: Beckman Coulter has identified that some Access PTH reagent packs from lot...

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

Class II — Potential Health HazardOngoing