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. 2,508 recalls have been distributed to Alabama in the last 12 months.
Showing 23081–23100 of 50,591 recalls
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...
The Issue: The MX40 may experience increased power consumption and may have a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...
The Issue: The MX40 may experience increased power consumption and may have a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...
The Issue: The MX40 may experience increased power consumption and may have a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T7 Driver Cannulated AO (Part Number 110018531) Product Usage: The Recalled...
The Issue: There is a potential of fracture, bending or shearing of the driver.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T7 Driver Solid AO (Part Number 110018541) Product Usage: The Recalled by...
The Issue: There is a potential of fracture, bending or shearing of the driver.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Recalled by Edwards Lifesciences, LLC Due to Difficulty...
The Issue: Difficulty with atrioseptostomy catheter balloon deflation after deployment,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Recalled by Edwards Lifesciences, LLC Due to Difficulty...
The Issue: Difficulty with atrioseptostomy catheter balloon deflation after deployment,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sea Salt 70% Dark Chocolate 3 oz. bars Recalled by Theo Chocolate Inc Due to...
The Issue: Theo Chocolate Sea Salt 70% Dark Chocolate Bar is recalled due to undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Thallous Chloride TI 201 Injection Recalled by Medi-Physics Inc. dba GE...
The Issue: Chemical Contamination: Trace amounts of an impurity was detected in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EZ Derm Porcine Xenograft Recalled by Molnlycke Health Care, Inc Due to...
The Issue: Intermittent heat seal failures on the outer pouch of some EZ Derm products.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pravastatin Sodium Tablets USP Recalled by Glenmark Pharmaceuticals Inc.,...
The Issue: Presence Of Foreign Tablet: in a bottle of Pravastatin Sodium Tablets 20 mg.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HAMILTON-G5 Recalled by Hamilton Medical AG Due to New software version for...
The Issue: New software version for affected ventilators reduces the probability of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Cardiology Hemo Recalled by Change Healthcare Israel Ltd. Due to...
The Issue: users are not notified of procedure medication discrepancies between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon Cardiology Hemo Recalled by Change Healthcare Israel Ltd. Due to...
The Issue: users are not notified of procedure medication discrepancies between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Testosterone Cypionate Injection Recalled by InvaGen Pharmaceuticals, Inc....
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate Injection Recalled by InvaGen Pharmaceuticals, Inc....
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate Injection Recalled by InvaGen Pharmaceuticals, Inc....
The Issue: Presence of Particulate Matter.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Biotin 10 mg/mL Injection Recalled by Auro Pharmacies Inc. DBA Central Drugs...
The Issue: Failed pH Specification: product does not meet pH label claim.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fayosim (levonorgestrel and ethinyl estradiol) tablets USP Recalled by Lupin...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Berchtold Chromophare F628 Surgical Lights. Product Usage: The medical...
The Issue: The back cover of the light head was insufficiently assembled and could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.