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. 2,448 recalls have been distributed to Alabama in the last 12 months.
Showing 35281–35300 of 50,591 recalls
Recalled Item: Morning Star Disaster Supplies Butternut Squash Soup Recalled by Wilderness...
The Issue: Wilderness Family Naturals Organic Coconut Milk Powder and other products...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Wilderness Family Naturals Coconut Chia Pudding Mix Sweetened with Coconut...
The Issue: Wilderness Family Naturals Organic Coconut Milk Powder and other products...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BD SurePathTM Preservative Collection Vials Recalled by Becton Dickinson &...
The Issue: BD has confirmed that a portion of BD SurePath" collection vials associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Paliperidone Extended-release Tablets Recalled by Mylan Pharmaceuticals Inc....
The Issue: Failed Dissolution Specifications; three month stability time point.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minocycline Hydrochloride Capsules USP Recalled by Apace KY LLC Due to...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: the individual blisters...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Scrub-Stat 4 (chlorhexidine gluconate) Foam Forming Solution Recalled by...
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: sulfur8 medicated LIGHT FORMULA (sulfur) anti-dandruff hair & scalp...
The Issue: Subpotent Drug: failed at the 3 and 6 month stability time points.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alendronate Sodium Tablets Recalled by Sun Pharma Global Fze Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Observed levels of highest...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IFS Web Bulk Pistachio Raw Shelled 80% Wholes Net Wt. Recalled by...
The Issue: Raw pistachios may be contaminated with Salmonella which was determined...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Valued Natural Raw Pistachio Kernels Net Wt 5 oz. (141 Recalled by...
The Issue: Raw pistachios may be contaminated with Salmonella which was determined...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sam International Bulk Raw Whole Pistachio 80% VP Net Wt. Recalled by...
The Issue: Raw pistachios may be contaminated with Salmonella which was determined...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: IFS Club Bag Pistachio Raw Shelled 80% Wholes Net Wt. Recalled by...
The Issue: Raw pistachios may be contaminated with Salmonella which was determined...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Organic traditions SPROUTED FLAX SEED POWDER Recalled by Health Matters...
The Issue: The repacked product has the potential to be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Organic traditions SPROUTED CHIA & FLAX SEED POWDER Recalled by Health...
The Issue: The repacked product has the potential to be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Accu-Chek Inform II Base Unit as a part of the Recalled by Roche Diagnostics...
The Issue: Accu-Chek Inform II Base Unit might produce physical transmission errors in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Insertion Tray Recalled by Arrow International, Inc., Division...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Insertion Tray Recalled by Arrow International, Inc., Division...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraFlex IAB: 7.5Fr 40cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FiberOptix Ultra 8 IAB: 8Fr 30cc The Arrow¿ IAB is Recalled by Arrow...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraFlex IAB: 7.5Fr 30cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.