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. 2,680 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,680 in last 12 months

Showing 31813200 of 28,641 recalls

Medical DeviceAugust 8, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Allura Xper systems (R8.1 with Poly-G Stand) Interventional...

The Issue: A half-threaded bolt was included in the LTE kits instead of the correct...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2024· Howmedica Osteonics Corp.

Recalled Item: MAKO Integrated Cutting System (MICS) HANDPIECE Recalled by Howmedica...

The Issue: Stryker has identified an issue with the characterization process that...

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: Pacemaker 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 Inguinal Hernia Graft C-IHM-10X15 - To reinforce soft tissues...

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: Hand Pack 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 Fistula Plug C-FPB-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: Vaginal Delivery 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: IR Procedure 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: Nasal Sinus 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: PACEMAKER 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: Neuro Vascular 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: Bilateral Tubal Ligation 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· Cook Biotech, Inc.

Recalled Item: Biodesign Recto-Vaginal Fistula Plug RVP-0.2 - 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-0.7-2 - 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: Paracentesis Thoracente 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· 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