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. 2,494 recalls have been distributed to Alabama in the last 12 months.
Showing 23341–23360 of 50,591 recalls
Recalled Item: icumedical ChemoClave Vented Vial Spike Recalled by ICU Medical, Inc. Due to...
The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxybutynin Chloride Recalled by Lannett Company Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Meijer Ultimate Chocolate Mint Chip Cookie Cookies in clear plastic Recalled...
The Issue: Undeclared soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ARIES Extraction Kit Recalled by Luminex Corporation Due to Through internal...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES HSV 1&2 Assay Recalled by Luminex Corporation Due to Through internal...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES C. difficile Assay Recalled by Luminex Corporation Due to Through...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES Flu A/B & RSV Assay Recalled by Luminex Corporation Due to Through...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES GBS Assay Recalled by Luminex Corporation Due to Through internal...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIES Group A Strep Assay Recalled by Luminex Corporation Due to Through...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aries Bordetella Assay Recalled by Luminex Corporation Due to Through...
The Issue: Through internal investigation, it was discovered that a portion of side...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXIBLE NEURO-FIBERSCOPE Recalled by Karl Storz Endoscopy Due to The action...
The Issue: The action is being initiated due to Flexible Neuroscopes manufactured with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CELL-DYN Emerald analyzer Recalled by Abbott Laboratories Due to There is a...
The Issue: There is a potential for the device to generate Quality Control (QC) low or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ 3600 Immunoassay System V3.3.2 & below Product Code: Recalled by...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ XT 7600 Integrated System-Software V3.4.1 & below Product Code:...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS ECi Immunodiagnostic System Product Code: 6801059 For use Recalled by...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ 5600 Integrated System V3.3.2 & below Product Code: Recalled by...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ 5600 Integrated System -Software V3.3.2 & below Product Code:...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ ECi/ECiQ Immunodiagnostic System Product Code: 1922814 For use in...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ 3600 Immunoassay System-Software V3.3.2 & below Product Code:...
The Issue: Luminometer Malfunction May Cause Inability to Process MicroWell Assays on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micro Knife 5.0mm 30¿ Recalled by Beaver Visitec Due to The product contains...
The Issue: The product contains a misprinted expiration date on the peel pack. Both...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.