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. 2,609 recalls have been distributed to Alabama in the last 12 months.
Showing 13121–13140 of 50,591 recalls
Recalled Item: Swanson Ultra: Vitamin B12 Methylcobalamin High Absorption 60 serving per...
The Issue: Dietary supplement may contain potential metal shavings greater than or...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold)...
The Issue: The product was distributed without FDA authorization or clearance for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drager Infinity CentralStation Software versions VG2.1.2 and VG2.1.2 SU12....
The Issue: Software issue resulting in temporary loss of central monitoring functionality.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare MR Systems Recalled by GE Healthcare, LLC Due to During the...
The Issue: During the de-installation of an MR system magnet, if all rigging and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Excelsior Medical 10mL Sterile Field Saline Flush ZR Recalled by MEDLINE...
The Issue: Sterility failure of the exterior of the syringe which may impact the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAND SANITIZER Isopropyl Alcohol Antiseptic 75% Recalled by Tennessee...
The Issue: Chemical Contamination: FDA analysis found 1 lot of HAND SANITIZER Isopropyl...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HAND SANITIZER Isopropyl Alcohol Antiseptic 75% Recalled by Tennessee...
The Issue: CGMP Deviations: lots and products of hand sanitizer are being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VESSEL SEALER EXTEND Recalled by Intuitive Surgical, Inc. Due to Placing...
The Issue: Placing excessive tissue in the instrument jaws of the devices prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DAVINCI | Energy SynchroSeal da Vinci X' da Vinci Xi' Recalled by Intuitive...
The Issue: Placing excessive tissue in the instrument jaws of the devices prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single- Use Duodenoscope (Box 2) UPN: M00542421 Recalled by...
The Issue: Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single- Use Duodenoscope (Box 1) UPN: M00542420 Recalled by...
The Issue: Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single-Use Duodenoscope (Box 1) UPN:M0054242CE0 Intended Use:...
The Issue: Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single-Use Duodenoscope (Box 2) UPN: M0054242CE1 Intended...
The Issue: Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Enhanced Estradiol (eE2) 500T - In vitro diagnostic Recalled...
The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Enhanced Estradiol (eE2) (REF) 500T - In vitro Recalled by...
The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Enhanced Estradiol (eE2) (REF) 500T - In vitro Recalled by...
The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Enhanced Estradiol (eE2) 500T - In vitro diagnostic Recalled by...
The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Enhanced Estradiol (eE2) 100T - In vitro diagnostic Recalled...
The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Enhanced Estradiol (eE2) 100T - In vitro diagnostic Recalled by...
The Issue: Falsely Elevated Results Observed with Plasma Specimens, could lead a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Aid Kits containing acetaminophen under brand names Equate (Walmart)...
The Issue: Kits contained recalled acetaminophen.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.