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. 2,494 recalls have been distributed to Alabama in the last 12 months.
Showing 23581–23600 of 50,591 recalls
Recalled Item: Cidofovir Injection 375mg/5mL (75mg/mL) vial injection. 5 mL vials Recalled...
The Issue: Lack of Assurance of Sterility: complaints received about dried powder on...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefdinir for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: CGMP Deviations: Product complaints received indicating reconstituted...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARCHITECT MAGNESIUM Recalled by Abbott Laboratories, Inc Due to Abbott...
The Issue: Abbott internal testing has identified that the Magnesium urine application...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica M220 F12 surgical microscope The Leica M220 F12 surgical Recalled by...
The Issue: The M220 optics may unintentionally drop into the surgical field, risking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curity All Purpose Sponges Recalled by Cardinal Health 200, LLC Due to...
The Issue: Curity All Purpose Sponges were not sterilized and distributed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexima Duodenal Bend Biliary Stent with Delivery System Recalled by Boston...
The Issue: The sterile barrier may contain packaging seal defects.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexima Duodenal Bend Biliary Stent with Delivery System Recalled by Boston...
The Issue: The sterile barrier may contain packaging seal defects.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vergene Amplification Tray - 700uL Recalled by Luminex Corporation Due to On...
The Issue: On lot of VERIGENE(R) BC-GP Utility Kits (20-011-018) were labeled with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATLAS Loading Car Recalled by Steris Corporation Due to The ATLAS loading...
The Issue: The ATLAS loading car may not remain fully engaged with the latch on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eclipse(TM) Treatment Planning System with Proton Convolution Superposition...
The Issue: There is an anomaly with the Eclipse(TM) Treatment Planning System [TPS]...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitrofurantoin Oral Suspension Recalled by LUPIN SOMERSET Due to Subpotent...
The Issue: Subpotent Drug: Expansion of June 2018 recall of lots S700065 and S700619...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Achieva XR 1.5T/3.0T Recalled by Philips Medical Systems Nederlands Due to...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for XR and 3.0T Recalled by Philips Medical Systems...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Achieva CV Nova Recalled by Philips Medical Systems Nederlands...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enterprise 1.5T Recalled by Philips Medical Systems Nederlands Due to There...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T Recalled by Philips Medical Systems Nederlands...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.0T Power/Pulsar Recalled by Philips Medical Systems Nederlands Due...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition X Recalled by Philips Medical Systems Nederlands Due to...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T Recalled by Philips Medical Systems Nederlands Due to There is...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR RT Recalled by Philips Medical Systems Nederlands Due to There is a...
The Issue: There is a potential for the ceiling speaker(s) to fall from their position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.