Product Recalls in Alabama

Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,684 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,684 in last 12 months

Showing 2140 of 50,591 recalls

Medical DeviceFebruary 6, 2026· Trividia Health, Inc.

Recalled Item: Owner's Booklets and Instructions for Use that are used with Recalled by...

The Issue: The system labeling (user manual and online labeling) did not provide...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 6, 2026· International Life Sciences

Recalled Item: Artelon FLEXBAND TWIST .12 3.85x17mm HEX Anchor (Qty Recalled by...

The Issue: Augmentation devices failed bacterial endotoxin testing.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2026· Trividia Health, Inc.

Recalled Item: Owner's Booklets and Instructions for Use that are used with Recalled by...

The Issue: The system labeling (user manual and online labeling) did not provide...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 6, 2026· Trividia Health, Inc.

Recalled Item: Owner's Booklets and Instructions for Use that are used with Recalled by...

The Issue: The system labeling (user manual and online labeling) did not provide...

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

Class I — Serious Health HazardOngoing
DrugFebruary 5, 2026· Fresenius Kabi Compounding, LLC

Recalled Item: vancomycin HCl Recalled by Fresenius Kabi Compounding, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 5, 2026· Remel, Inc

Recalled Item: Campy CVA Medium 100/PK Recalled by Remel, Inc Due to Customer complaints...

The Issue: Customer complaints report low to no recovery of Campylobacter Jejuni ATCC...

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

Class II — Potential Health HazardOngoing
DrugFebruary 5, 2026· Fresenius Kabi Compounding, LLC

Recalled Item: vancomycin HCl Recalled by Fresenius Kabi Compounding, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 5, 2026· Fresenius Kabi Compounding, LLC

Recalled Item: ketamine HCl Recalled by Fresenius Kabi Compounding, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 5, 2026· Fresenius Kabi Compounding, LLC

Recalled Item: thiamine HCl Recalled by Fresenius Kabi Compounding, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 5, 2026· Fresenius Kabi Compounding, LLC

Recalled Item: acyclovir sodium Recalled by Fresenius Kabi Compounding, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 4, 2026· Diagnostica Stago, Inc.

Recalled Item: Brand Name: STA Liatest Free Protein S Product Name: STA Recalled by...

The Issue: The potential of out-of-range results and an underestimation of the free...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2026· Ion Beam Applications S.A.

Recalled Item: IBA Proton Therapy System - PROTEUS 235 Recalled by Ion Beam Applications...

The Issue: It was identified that eh Universal Beam Triggering Interface (UBTI) is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2026· B Braun Medical Inc

Recalled Item: Brand Name: B. Braun Product Name: 21GA WINGED INFUSION Recalled by B Braun...

The Issue: The potential for the needle tip to be dull/blunt, difficult to advance,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2026· B Braun Medical Inc

Recalled Item: Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM Recalled by B...

The Issue: The potential for the needle tip to be dull/blunt, difficult to advance,...

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

Class II — Potential Health HazardOngoing
DrugFebruary 2, 2026· Pro Numb Tattoo Numbing Spray LLC

Recalled Item: Pro Numb Tattoo Numbing Spray Recalled by Pro Numb Tattoo Numbing Spray LLC...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 2, 2026· B Braun Medical Inc

Recalled Item: Brand Name: B. Braun Product Name: 21GA WINGED INF SET Recalled by B Braun...

The Issue: The potential for the needle tip to be dull/blunt, difficult to advance,...

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

Class II — Potential Health HazardOngoing
DrugFebruary 2, 2026· Pro Numb Tattoo Numbing Spray LLC

Recalled Item: Pro Numb Tattoo Numbing Spray Recalled by Pro Numb Tattoo Numbing Spray LLC...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 30, 2026· Medline Industries, LP

Recalled Item: Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit:...

The Issue: The instructions for use (IFUs) on specified Cardinal Health Chest Drainage...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2026· Beckman Coulter Mishima K.K.

Recalled Item: DxC 700 AU Recalled by Beckman Coulter Mishima K.K. Due to A delay in...

The Issue: A delay in results may occur. When clinical chemistry analyzer calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2026· Covidien LLC

Recalled Item: HealthCast "Vital Sync" Remote Patient Monitoring System which consists of:...

The Issue: Due to complaints and investigations stating that alarms from the primary...

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

Class II — Potential Health HazardOngoing