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. 1,814 recalls have been distributed to Alabama in the last 12 months.
Showing 35221–35240 of 50,591 recalls
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyrogen (thyrotropin alfa for injection) Recalled by Genzyme Corporation...
The Issue: Presence of Particulate Matter: Glass particles found in the product after...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyrogen (thyrotropin alfa for injection) Recalled by Genzyme Corporation...
The Issue: Presence of Particulate Matter: Glass particles found in the product after...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BIG BOB GIBSON B-B-Q Seasoning and dry rub Recalled by Ingredients...
The Issue: Glass shards were found in a sealed bag of dehydrated minced garlic. Parts...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ICA GOURMET SEASONINGS Recalled by Ingredients Corporation Of America Due to...
The Issue: Glass shards were found in a sealed bag of dehydrated minced garlic. Parts...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: C & J BUTCHER SHOP Recalled by Ingredients Corporation Of America Due to...
The Issue: Glass shards were found in a sealed bag of dehydrated minced garlic. Parts...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KD's GOOD STUFF SEASONING Recalled by Ingredients Corporation Of America Due...
The Issue: Glass shards were found in a sealed bag of dehydrated minced garlic. Parts...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ICA GOURMET SEASONINGS Recalled by Ingredients Corporation Of America Due to...
The Issue: Glass shards were found in a sealed bag of dehydrated minced garlic. Parts...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ICA GOURMET SEASONINGS Recalled by Ingredients Corporation Of America Due to...
The Issue: Glass shards were found in a sealed bag of dehydrated minced garlic. Parts...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 4.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.5 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.0 mm and 7.3 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5 mm Cancellous Screw Recalled by Synthes (USA) Products LLC Due to...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.5 mm and 4.0 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.0 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.