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. 2,377 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,377 in last 12 months

Showing 4832148340 of 50,591 recalls

FoodNovember 8, 2012· Nestle USA

Recalled Item: Nesquik Chocolate Powder Recalled by Nestle USA Due to Potential Salmonella...

The Issue: Nestle is recalling Nesquik Chocolate Powder because certain lots of its...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 8, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: ShapeMatch Cutting Guides Product Usage: The ShapeMatch Cutting Guides are...

The Issue: With regards to ShapeMatch Cutting Guides using MRI Imaging, Stryker...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 8, 2012· Toshiba American Medical Systems Inc

Recalled Item: Toshiba Infinix-i X-Ray System. A radiographic and fluoroscopic x-ray system...

The Issue: Lost and incorrect images. When using the "F-Rec" fluoroscopy image...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2012· Medline Industries Inc

Recalled Item: Medline Angio Drape Pack Radiology-LF Recalled by Medline Industries Inc Due...

The Issue: The non-sterile Waste Bag component in the custom pack was attached to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 8, 2012· MOOG Medical Devices Group

Recalled Item: EnteraLite Infinity Enteral Feeding Pump identified with the following list...

The Issue: MOOG Medical Devices Group is conducting a voluntary for a limited set of...

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

Class II — Potential Health HazardOngoing
FoodNovember 7, 2012· Reaction Nutrition LLC

Recalled Item: Clinical LIVE Dietary Supplement Immune Support 694.325 mg 90 capsules...

The Issue: The product contained an undeclared allergen, Colostrum, which is considered...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 8 X80MM Tl Product Recalled by DePuy Spine,...

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 10 X 80MM Tl Recalled by DePuy Spine, Inc....

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 8 X100MM Tl Product Recalled by DePuy...

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 8 X70MM Tl Product Recalled by DePuy Spine,...

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 10X100MM Tl Product Code: Recalled by DePuy...

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 9 X 80MM Tl Recalled by DePuy Spine, Inc....

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 9 X100MM Tl Product Recalled by DePuy...

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 9 X70MM Tl Product Recalled by DePuy Spine,...

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 10 X 70MM Tl Recalled by DePuy Spine, Inc....

The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2012· IDS (Immunodiagnostic Systems Ltd.)

Recalled Item: 25-Hydroxy Vitamin D EIA Recalled by IDS (Immunodiagnostic Systems Ltd.) Due...

The Issue: Immunodiagnostic Systems is recalling the 25-Hydroxy Vitamin D EIA, AC-57F1...

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

Class II — Potential Health HazardOngoing
DrugNovember 6, 2012· Alkermes, Inc.

Recalled Item: VIVITROL (naltrexone for extended-release injectable suspension) a) 380 mg...

The Issue: Lack of Assurance of Sterility: Product did not meet the criteria for...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 6, 2012· Omya Inc

Recalled Item: Ground limestone also known as calcium carbonate. Omya's food grade Recalled...

The Issue: Omya Inc. is voluntarily recalling certain lots of food grade ground...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 6, 2012· Ethicon Endo-Surgery Inc

Recalled Item: Ethicon Endo-Surgery Inc. The ENSEAL¿ G2 Tissue Sealers are indicated...

The Issue: Potential for self activation while the device is in use, which may result...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2012· Invacare Corporation

Recalled Item: Invacare Height Adjustable (walking) Canes Recalled by Invacare Corporation...

The Issue: Following their receipt of several customer complaints, Invacare recalled...

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

Class II — Potential Health HazardOngoing