Product Recalls in Missouri
Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,918 recalls have been distributed to Missouri in the last 12 months.
Showing 23901–23920 of 52,570 recalls
Recalled Item: BD Synapsys Laboratory Solutions Catalog Number:444150 Product Usage: BD...
The Issue: BD Synapsys version 2.1 allowed the potential for a test order to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Best Choice Pancake & Waffle Complete Mix Original 32oz. retail carton...
The Issue: Undeclared milk. Buttermilk pancake mix which contains milk was packed in...
Recommended Action: Do not consume. Return to store for a refund or discard.
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: 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: 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: 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: 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: 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¿ 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¿ 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 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¿ 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¿ 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: 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: Lovastatin Tablets USP Recalled by American Health Packaging Due to CGMP...
The Issue: CGMP Deviations: Finished product made with lovastatin drug substance that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.