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. 2,660 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,660 in last 12 months

Showing 46814700 of 50,591 recalls

Medical DeviceAugust 7, 2024· American Contract Systems, Inc.

Recalled Item: Cath Lab Pack Recalled by American Contract Systems, Inc. Due to ACS...

The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· American Contract Systems, Inc.

Recalled Item: Endovascular AAA Pack Recalled by American Contract Systems, Inc. Due to ACS...

The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· American Contract Systems, Inc.

Recalled Item: Shoulder Recalled by American Contract Systems, Inc. Due to ACS identified...

The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· Cook Biotech, Inc.

Recalled Item: Biodesign Recto-Vaginal Fistula Plug RVP-0.7 - For implantation to reinforce...

The Issue: Products expire prior to the expiration date printed on the product labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· Cook Biotech, Inc.

Recalled Item: Biodesign Fistula Plug C-FPS-0.4-2 - For implantation to reinforce soft...

The Issue: Products expire prior to the expiration date printed on the product labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· American Contract Systems, Inc.

Recalled Item: Cysto Recalled by American Contract Systems, Inc. Due to ACS identified that...

The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· Cook Biotech, Inc.

Recalled Item: Biodesign Fistula Plug C-FPS-0.2 - For implantation to reinforce soft...

The Issue: Products expire prior to the expiration date printed on the product labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· Cook Biotech, Inc.

Recalled Item: Biodesign Fistula Plug C-FPB-0.4 - For implantation to reinforce soft...

The Issue: Products expire prior to the expiration date printed on the product labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· American Contract Systems, Inc.

Recalled Item: Essentia MAJ Laparotomy Std Pack Recalled by American Contract Systems, Inc....

The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· American Contract Systems, Inc.

Recalled Item: Day Surgery General Pack Recalled by American Contract Systems, Inc. Due to...

The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· Cook Biotech, Inc.

Recalled Item: Biodesign Fistula Plug C-FPS-0.2-2 - For implantation to reinforce soft...

The Issue: Products expire prior to the expiration date printed on the product labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· Cook Biotech, Inc.

Recalled Item: Biodesign Recto-Vaginal Fistula Plug RVP-0.4 - For implantation to reinforce...

The Issue: Products expire prior to the expiration date printed on the product labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· American Contract Systems, Inc.

Recalled Item: ENT Recalled by American Contract Systems, Inc. Due to ACS identified that...

The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· Cook Biotech, Inc.

Recalled Item: Biodesign Fistula Plug C-FPS-0.7 - For implantation to reinforce soft...

The Issue: Products expire prior to the expiration date printed on the product labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· American Contract Systems, Inc.

Recalled Item: Arthroscopy Pack Recalled by American Contract Systems, Inc. Due to ACS...

The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· American Contract Systems, Inc.

Recalled Item: Open Shoulder Recalled by American Contract Systems, Inc. Due to ACS...

The Issue: ACS identified that due to an inoperable chart recorder, humidity readings...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· Cook Biotech, Inc.

Recalled Item: Biodesign Fistula Plug C-FPS-0.4 - For implantation to reinforce soft...

The Issue: Products expire prior to the expiration date printed on the product labeling

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· BioFire Diagnostics, LLC

Recalled Item: FILMARRAY 2.0 INSTRUMENT Recalled by BioFire Diagnostics, LLC Due to...

The Issue: Some automated in vitro diagnostic modules and instruments manufactured or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· B Braun Medical Inc

Recalled Item: Infusomat Space Infusion System/ Large Volume Pump Recalled by B Braun...

The Issue: Extension of previous recall RES 92978. Pumps have the potential for...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 7, 2024· BioFire Diagnostics, LLC

Recalled Item: FILMARRAY TORCH MODULE BOX Recalled by BioFire Diagnostics, LLC Due to...

The Issue: Some automated in vitro diagnostic modules and instruments manufactured or...

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

Class II — Potential Health HazardOngoing