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. 2,509 recalls have been distributed to Alabama in the last 12 months.
Showing 20881–20900 of 50,591 recalls
Recalled Item: Dario Blood Glucose Monitoring System Recalled by LABSTYLE INNOVATIONS Due...
The Issue: The Dario-Blood Glucose Tracker Android App versions 4.3.0-4.3.2 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVKARE Fexofenadine Hydrochloride Tablets USP Antihistamine 180 mg Recalled...
The Issue: Failed Stability Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Centurion CIRCLAMP W/1.3 CM BELL-single-use Recalled by Centurion Medical...
The Issue: A mismatch between the angle of the hole in the base and the angle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas c 701 and 702 Analyzer/Module-RF interference claims for the Recalled...
The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion CIRCLAMP W/1.1CM BELL - single-use Recalled by Centurion Medical...
The Issue: A mismatch between the angle of the hole in the base and the angle of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas c 311 Recalled by Roche Diagnostics Operations, Inc. Due to Tina-quant...
The Issue: Tina-quant Soluble Transferrin Receptor (STFR) Assays Updated Claims for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lamivudine Tablets Recalled by American Health Packaging Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Package Insert; an error in the Dosage Forms...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Karl Storz NEURO-FIBERSCOPE Recalled by Karl Storz Endoscopy Due to During a...
The Issue: During a complaint investigation it was determined that an error was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz RHINO-LARYNGO-BRONCHO FIBERSCOPE Recalled by Karl Storz Endoscopy...
The Issue: During a complaint investigation it was determined that an error was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz Recalled by Karl Storz Endoscopy Due to During a complaint...
The Issue: During a complaint investigation it was determined that an error was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Low Volume Cartridge IFU (SKU CAR-125-B) used with the following Recalled by...
The Issue: There is a potential patient health risk while performing chronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Martha White Gluten Free Sweet Yellow Cornbread & Muffin Mix Recalled by...
The Issue: Product tested positive for gluten but is labeled as Gluten free
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PediaSmart Organic Soy Vanilla Beverage Mix Recalled by Natures One Inc Due...
The Issue: Undeclared milk allergen.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Positron Emission Tomograpy and Computed Tomography System Recalled by...
The Issue: Potential sporadic software bugs in R001.3.0.0.750505 software version may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Entropic Labs SARM RAD-140 Recalled by Tuscano and Delucia Group (DBA...
The Issue: Marketed Without An Approved NDA/ANDA: product contains Selective Androgen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fexofenadine hydrochloride tablets USP Recalled by Aurolife Pharma, LLC Due...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fexofenadine Hydrochloride Tablets USP Recalled by Aurolife Pharma, LLC Due...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wal-Fex (Fexofenadine Hydrochloride) Tablets USP Recalled by Aurolife...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Allergy (Fexofenadine Hydrochloride) Tablets USP Recalled by Aurolife...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fexofenadine HCL Tablets USP Recalled by Aurolife Pharma, LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.