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. 2,467 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,467 in last 12 months

Showing 3212132140 of 50,591 recalls

FoodOctober 28, 2016· Aldi Inc

Recalled Item: Simply Nature Organic Red Split Lentils Recalled by Aldi Inc Due to...

The Issue: Product may contain undeclared wheat

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 28, 2016· Aldi Inc

Recalled Item: Simply Nature Organic Green Lentils Recalled by Aldi Inc Due to Undeclared Wheat

The Issue: Product may contain undeclared wheat

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 28, 2016· Life Rising Corp S

Recalled Item: Life Rising TT Side Head Regulator Recalled by Life Rising Corp S Due to...

The Issue: High levels of lead discovered in product.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 28, 2016· Mondelez International

Recalled Item: Nabisco Oreo Fudge Creme Original Variety Recalled by Mondelez International...

The Issue: Mondelez Global LLC is recalling certain Oreo Fudge Cremes (Original and...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 28, 2016· Mondelez International

Recalled Item: Nabisco Oreo Fudge Creme Mint Variety Recalled by Mondelez International Due...

The Issue: Mondelez Global LLC is recalling certain Oreo Fudge Cremes (Original and...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 28, 2016· Ion Beam Applications S.A.

Recalled Item: 12C (AdaPTinsight) Affected component: AdaPTinsight software Product Usage:...

The Issue: IBA is initiating this recall to address an issue identified with...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2016· The Binding Site Group, Ltd.

Recalled Item: Freelite Human Lambda Free Kit for use on SPAPLUS Product Code: LK018.S...

The Issue: A change in the calibration curve causing an increase in false prozone flags.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2016· Aesculap Implant Systems LLC

Recalled Item: Gomco Circumcision Clamps with separate O-Ring Component: The device is...

The Issue: Aesculap has received complaints of excessive bleeding after use of Gomco...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2016· Natus Medical Incorporated

Recalled Item: Natus neoBLUE blanket LED Phototherapy system Recalled by Natus Medical...

The Issue: neoBLUE blanket LED Phototherapy System distributed since release of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2016· Hologic, Inc

Recalled Item: SURESOUND22US Multipack (US Distribution) containing 2 packs of six devices....

The Issue: Breach in sterile barrier compromising product sterility

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

Class II — Potential Health HazardOngoing
DrugOctober 27, 2016· Amerisource Health Services

Recalled Item: Bupropion Hydrochloride Extended-Release Tablets Recalled by Amerisource...

The Issue: Failed Dissolution Specifications: The firm was notified that there was a...

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

Class III — Low RiskOngoing
Refund
FoodOctober 27, 2016· Back To Nature Foods, Llc

Recalled Item: Back to Nature Mini Chocolate Chunk Cookies Recalled by Back To Nature...

The Issue: Produces contains undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 27, 2016· Back To Nature Foods, Llc

Recalled Item: Back to Nature Recalled by Back To Nature Foods, Llc Due to Undeclared Milk

The Issue: Produces contains undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 27, 2016· Back To Nature Foods, Llc

Recalled Item: Back to Nature Chocolate Chunk Cookies Recalled by Back To Nature Foods, Llc...

The Issue: Produces contains undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 27, 2016· Back To Nature Foods, Llc

Recalled Item: Back to Nature Recalled by Back To Nature Foods, Llc Due to Undeclared Milk

The Issue: Produces contains undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: Mucosal Atomization Device (MAD) Recalled by Teleflex Medical Due to Product...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: LMA MADomizer Recalled by Teleflex Medical Due to Product Defect; These...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: LMA MADdy Recalled by Teleflex Medical Due to Product Defect; These products...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: LMA MADett Recalled by Teleflex Medical Due to Product Defect; These...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2016· Teleflex Medical

Recalled Item: FLEXI NOZZLE LONG Recalled by Teleflex Medical Due to Product Defect; These...

The Issue: Product Defect; These products may produce a straight stream instead of a...

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

Class II — Potential Health HazardOngoing