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. 2,429 recalls have been distributed to Alabama in the last 12 months.
Showing 39901–39920 of 50,591 recalls
Recalled Item: Charleys Recalled by Lavoi Corporation d/b/a/ Epi De France Due to...
The Issue: Undeclared allergen: Bread products were manufactured using raw material...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Epi breads Recalled by Lavoi Corporation d/b/a/ Epi De France Due to...
The Issue: Undeclared allergen: Bread products were manufactured using raw material...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Epi breads Recalled by Lavoi Corporation d/b/a/ Epi De France Due to...
The Issue: Undeclared allergen: Bread products were manufactured using raw material...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Epi breads Recalled by Lavoi Corporation d/b/a/ Epi De France Due to...
The Issue: Undeclared allergen: Bread products were manufactured using raw material...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Epi breads Recalled by Lavoi Corporation d/b/a/ Epi De France Due to...
The Issue: Undeclared allergen: Bread products were manufactured using raw material...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zaxbys Recalled by Lavoi Corporation d/b/a/ Epi De France Due to Undeclared...
The Issue: Undeclared allergen: Bread products were manufactured using raw material...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medtronic Recalled by Medtronic Inc. Cardiac Rhythm Disease Management Due...
The Issue: Clinicians observed debris, appearing to originate from the hemostasis valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RECLAIM Assembled Implant Inserter Adaptor orthopedic manual surgical...
The Issue: This lot of the RECLAIM Assembled Implant Inserter Adaptor Instrument may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROMETHAZINE DM SYRUP (Promethazine Hydrochloride Recalled by Qualitest...
The Issue: Presence of Foriegn Substance: Plastic cap closure particulates may be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atracurium Besylate Injection Recalled by Sagent Pharmaceuticals Inc Due to...
The Issue: Lack of Assurance of Sterility: Recall initiated due to FDA observations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atracurium Besylate Injection Recalled by Sagent Pharmaceuticals Inc Due to...
The Issue: Lack of Assurance of Sterility: Recall initiated due to FDA observations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mobius3D Product Usage: Mobius3D software is used for quality assurance...
The Issue: Mobius3D version 1.5.0 contained a defect in software code which affects...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 Series Hemodialysis Machines: 2008K with the following product code...
The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 Series Hemodialysis Machines: 2008T with the following product code...
The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OptiMedica Catalys Precision Laser System Recalled by Abbott Medical Optics,...
The Issue: Device may experience loss of suction during treatment resulting in scoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 Series Hemodialysis Machines: 2008Kathome - 190895 2008T GEN 2 Recalled...
The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coblator II System Recalled by ArthroCare Medical Corporation Due to The...
The Issue: The recalling firm was notified by the contract manufacturer that they had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GAP Nail 4.8mm (diameter size) of the GAP ENDO-EXO MEDULLARY Recalled by...
The Issue: Failures of the 4.8mm of the GAP Endo-Exo Medullary System have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalys Precision Laser System-Catalys - U - US product Recalled by...
The Issue: Software anomaly on OptiMedica CATALYS System version 3.00.05 that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 Series Hemodialysis Machines: 2008K2 with the following product code...
The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.