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 38661–38680 of 50,591 recalls
Recalled Item: Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit with Sunscreen Recalled by...
The Issue: Microbial Contamination of Non-Sterile Products: Product failed USP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ortho-Cept (0.15 mg desogestrel and 0.03 mg ethinyl estradiol) tablets...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lerner Laboratories Mucolexx Recalled by Richard-Allan Scientific Company...
The Issue: Richard Allan Scientific (RAS) is initiating a recall of Mucolytic agent and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and...
The Issue: Complaints with the HVAD Internal Controller Alarm Battery failures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac...
The Issue: Complaints with the HVAD Discolored and Cracked Driveline Outer Sheath.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cortical Screw for M/DN Intramedullary Fixation. Metaphyseal/Diaphyseal Nail...
The Issue: The entire scope of 4.5mm Cortical Screws listed as compatible with the M/DN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD) Pump Driveline Splice Kit Product...
The Issue: Failures of the splice repair kit if exposed to excessive force.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mucolytic Agent 1 pint/473 ml Recalled by Richard-Allan Scientific Company...
The Issue: Richard Allan Scientific (RAS) is initiating a recall of Mucolytic agent and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyLink Data Management System Recalled by Siemens Healthcare Diagnostics,...
The Issue: System Limitations and Software Issues related to the following features:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac...
The Issue: Complaints with the HVAD Abnormal Power Source Switching.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #: 1101 Recalled by...
The Issue: Complaints with the HVAD Retraction of Pins within the driveline connector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and...
The Issue: HeartWare has received complaints relating to damage or bent connection pins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azithromycin Tablets Recalled by PD-Rx Pharmaceuticals, Inc. Due to cGMP...
The Issue: cGMP Deviations: This recall is a result of the original manufacturer's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azithromycin 500 mg tablets Recalled by PD-Rx Pharmaceuticals, Inc. Due to...
The Issue: cGMP Deviations: This recall is a result of the original manufacturer's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adrucil (fluorouracil injection Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Presence of Particulate Matter: Black particulate matter was identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KABIVEN [(3.9%) Lipid Injectable Emulsion with (3.1%) Amino Acids and...
The Issue: Labeling: Label Error on Declared Strength: Labeled 3.1% Amino Acids but...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Alcon Custom Pak. The Alcon Customer Pak is an Recalled by Alcon...
The Issue: The supplier of the Devon Light Glove, a component of the Alcon Custom PAK,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by MRP, LLC dba AMUSA Due to...
The Issue: Incorrect expiration date on label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Surgical Kits containing Medtronic Covidien Devon(TM) Light Gloves:...
The Issue: Surgical kits contain Medtronic Covidien Devon(TM) Light Gloves which were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRIT-LINE Blood Chamber- an accessory to the Crit line III- Recalled by...
The Issue: Blood chamber connection leaks during the use of the CRIT-LINE¿ Blood Chamber
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.