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. 2,467 recalls have been distributed to Alabama in the last 12 months.
Showing 28741–28760 of 50,591 recalls
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...
The Issue: A delay in transit may have contributed to nonconformity as the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PC-1000 Recalled by Panoramic Rental Corp. Due to The lift motor used to...
The Issue: The lift motor used to raise and lower the overhead chassis will wear if not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Euphora Rapid Exchange Balloon Dilatation Catheter Recalled by Medtronic...
The Issue: Stylette removal difficulties on the Euphora and Solarice products.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ReNew Reusable Grasper and Dissector Tips are to be Recalled by...
The Issue: The heat-shrink insulation tube may split during autoclave...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solarice Rapid Exchange Balloon Dilatation Catheter Recalled by Medtronic...
The Issue: Stylette removal difficulties on the Euphora and Solarice products.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chlorhexidine Gluconate Oral Rinse Recalled by Akorn Inc Due to...
The Issue: Crystallization with subpotent out of specification assay results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Deferoxamine Mesylate for injection Recalled by Pfizer Inc. Due to CGMP...
The Issue: CGMP Deviations: Firm failed to control impurity for color change at the API...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Halyard 24-Hour Oral Care Kit q4 Recalled by Akorn Inc Due to...
The Issue: Crystallization with subpotent out of specification assay results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Halyard 24-Hour Oral Care Kit q2 Recalled by Akorn Inc Due to...
The Issue: Crystallization with subpotent out of specification assay results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pravastatin Sodium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: high out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brilliance iCT SP - Model 728311 Brilliance iCT - Model Recalled by Philips...
The Issue: Numerous software issues with Brilliance iCT 4.1.6 version. Issues affect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT - Model 728306 Computed Tomography X-ray systems Recalled by...
The Issue: Numerous software issues with Brilliance iCT 4.1.6 version. Issues affect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Scientific Solutions Americas Corporation ( OSSA ) Model: VANTA...
The Issue: Instruments may, under certain specific circumstances listed below, fail to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Qualigen(R) The FastPack(R) IP Vitamin D Complete Immunoassay Kit Recalled...
The Issue: Specific lots have been reported to produce falsely lower than expected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ondamed Biofeedback Device Recalled by Ondamed Inc Due to The firm was...
The Issue: The firm was marketing the Ondamed System in the US without marketing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceres Self-Drilling Variable Screw 4.0 x 12mm The Ceres screws Recalled by...
The Issue: Incorrect direct marking and color identification for the affected lot of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fogarty Adherent Clot Catheter Model Numbers 1408010 and 140806 Product...
The Issue: The diameter of the Fogarty Catheter balloon, measures 6mm instead of 10mm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.