Product Recalls in Mississippi
Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,590 recalls have been distributed to Mississippi in the last 12 months.
Showing 13201–13220 of 49,744 recalls
Recalled Item: The IFU for the Autoclavable Temperature Probes: Part # 453564635891...
The Issue: Update to instructions for use regarding the cleaning and disinfection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brius Patient Specific Brackets (components in a set of custom Recalled by...
The Issue: Pontics, brackets, and customized orthodontic appliances were sold and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Customized Brius Appliances (custom metal orthodontic devices) Recalled by...
The Issue: Pontics, brackets, and customized orthodontic appliances were sold and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brius Pontics (components in a set of custom metal orthodontic devices)...
The Issue: Pontics, brackets, and customized orthodontic appliances were sold and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prevantics (chlorhexidine gluconate and isopropyl alcohol) Swab Recalled by...
The Issue: cGMP deviations: uncertainty of the adequacy of the validation of the test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prevantics (chlorhexidine gluconate and isopropyl alcohol) Maxi Swabstick...
The Issue: cGMP deviations: uncertainty of the adequacy of the validation of the test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prevantics (chlorhexidine gluconate and isopropyl alcohol) Swabstick...
The Issue: cGMP deviations: uncertainty of the adequacy of the validation of the test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PARAGARD T380A (intrauterine copper contraceptive) Recalled by...
The Issue: Non-sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MegMan Performance Booster Recalled by Junp Hydration LLC Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips Recalled by Philips North America LLC Due to There is a potential...
The Issue: There is a potential for AED pads to experience gel separation from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Recalled by Philips North America LLC Due to There is a potential...
The Issue: There is a potential for AED pads to experience gel separation from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic TurboHawk Plus Directional Atherectomy System 6F Recalled by ev3...
The Issue: The device has similarities in design to another device that the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic TurboHawk Plus Directional Atherectomy System 6F Recalled by ev3...
The Issue: The device has similarities in design to another device that the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiovascular Procedure Kit catalog # 76645 & 73806 Recalled by Terumo...
The Issue: Potential for Cardiovascular Procedure Kit packaging damage that occurred...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MM-TSM (Touch Screen Module/Secondary Controller/Bedside Controller)...
The Issue: Multi-Modality Touch Screen Modules (MM-TSM), used with integrated IVUS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity s System software version2.8.0 Recalled by Abbott Laboratories, Inc...
The Issue: Software error associated with the immunoassay analyzer wash cycle which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: El Chavito¿ Saladitos Dried Salted Plums Recalled by El Chavito Due to...
The Issue: Potential to be contaminated with lead.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: El Chavito¿ Saladitos Enchilados Salted Plums with Chili Recalled by El...
The Issue: Potential to be contaminated with lead.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Philips StentBoost Live R2.0 application Recalled by Philips Healthcare Due...
The Issue: Due to an incorrect configuration setting in the EPX database of StentBoost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura (Model Numbers 722010 Recalled by Philips North America Llc...
The Issue: Due to a software defect, the Philips StentBoost Live R2.0 might not process...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.