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. 2,442 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,442 in last 12 months

Showing 3732137340 of 50,591 recalls

Medical DeviceAugust 18, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software and firmware bugs

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2015· Brainlab AG

Recalled Item: Disposable Marker Spheres The Disposable Marker Spheres used Recalled by...

The Issue: Disposable Marker Spheres (DRMS) for Brainlab Image Guided Surgery (IGS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2015· Zien Medical Technologies, Inc

Recalled Item: PenBlade Safety Scalpel Recalled by Zien Medical Technologies, Inc Due to...

The Issue: Cracks were discovered in the PET tray of a small population of sterile...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2015· St Jude Medical Cardiac Rhythm Management Division

Recalled Item: Merlin@home RF Remote Monitoring Transmitter Model EX1150. Intended to aid...

The Issue: Some devices exhibit backup VVI operation due to a backup reset.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2015· Medtronic Perfusion Systems

Recalled Item: MEDTRONIC PERFUSION TUBING PACKS (with potentially affected...

The Issue: Hemocor High Performance Hemoconcentrators demonstrate low ultrafiltration...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2015· Medtronic Perfusion Systems

Recalled Item: MEDIVATORS HEMOCOR HPH700 Recalled by Medtronic Perfusion Systems Due to...

The Issue: Hemocor High Performance Hemoconcentrators demonstrate low ultrafiltration...

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

Class II — Potential Health HazardOngoing
DrugAugust 17, 2015· Apotex Inc.

Recalled Item: Cevimeline Hydrochloride Capsules Recalled by Apotex Inc. Due to Failed...

The Issue: Failed Stability Specifications: product may not meet specification limit...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 17, 2015· Bausch & Lomb, Inc.

Recalled Item: Bromfenac Ophthalmic Solution Recalled by Bausch & Lomb, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility: Failed preservative effectiveness testing.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 17, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet Getinge Group Recalled by Maquet Cardiovascular Us Sales, Llc Due to...

The Issue: Two serious thromboembolic events were reported involving the Adjustable...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet Getinge Group Recalled by Maquet Cardiovascular Us Sales, Llc Due to...

The Issue: Two serious thromboembolic events were reported involving the Adjustable...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: CIOS ALPHA Recalled by Siemens Medical Solutions USA, Inc Due to patient...

The Issue: patient procedure interruption due to a potential system failure

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2015· Intuitive Surgical, Inc.

Recalled Item: da Vinci Xi Surgical System P4 software Recalled by Intuitive Surgical, Inc....

The Issue: Complaints regarding the Exposed Knife Blade recoverable fault for the Xi...

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

Class II — Potential Health HazardOngoing
FoodAugust 14, 2015· Anhing Corporation

Recalled Item: Caravelle ABC Cookies Banh Chu NET WT: 7oz (200gr) Product of Vietnam...

The Issue: Anhing Corporation is recalling Caravelle ABC Cookies because recent...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 14, 2015· Toshiba American Medical Systems Inc

Recalled Item: INFX-8000V Bi-Plane X-Ray Interventional System X-ray systems Recalled by...

The Issue: When a fontal DA (Digital Angiography) acquisition was done, scattered x-ray...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Edge Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: software bug issues for SW-Version VA48A_SP0. The following safety issues...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2015· Limacorporate S.p.A

Recalled Item: SMR Shoulder/Spalla Trial Heads ECC .4 mm Adaptor Recalled by Limacorporate...

The Issue: The dimensions of the mating features of the recalled products are out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2015· Limacorporate S.p.A

Recalled Item: SMR Shoulder/Spalla Trial Humeral Head diameter .42 mm Recalled by...

The Issue: The dimensions of the mating features of the recalled products are out of...

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

Class II — Potential Health HazardOngoing
DrugAugust 13, 2015· GlaxoSmithKline, LLC.

Recalled Item: Bactroban Ointment (mupirocin calcium) Recalled by GlaxoSmithKline, LLC. Due...

The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...

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

Class II — Potential Health HazardOngoing
Refund