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. 2,448 recalls have been distributed to Mississippi in the last 12 months.
Showing 32421–32440 of 49,744 recalls
Recalled Item: CURVED-TIP STAPLER 30 Recalled by Intuitive Surgical, Inc. Due to Field...
The Issue: Field failures were reported related to the da Vinci Xi Surgical System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Bone Level Implant Recalled by Straumann Manufacturing, Inc. Due...
The Issue: Misalignment with the Loxim transfer piece markings, the positioning of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Bone Level Implant Recalled by Straumann Manufacturing, Inc. Due...
The Issue: Misalignment with the Loxim transfer piece markings, the positioning of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Estradiol Reagent Pack Recalled by...
The Issue: Ortho Clinical Diagnostics has issued a recall of their VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIAISON Estradiol II Gen Recalled by Diasorin Inc. Due to DiaSorin is...
The Issue: DiaSorin is issuing an urgent medical device correction for the LIAISON¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Q AND Q.ZEN- MODULAR ANGIOGRAPHIC SYSTEM Recalled by Siemens Medical...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS ZEE AND ZEEGO Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM Recalled by Siemens Medical Solutions...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6F/7F MynxGrip Vascular Closure Device Recalled by AccessClosure, Inc., A...
The Issue: A total of 70 6F/7F Mynx Grip devices were shipped from a distributor using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trokendi XR (topiramate) extended-release capsule Recalled by Supernus...
The Issue: Superpotent Drug: Failure of assay specifications in the capsule.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Breaded stuffed Jalapenos poppers labeled in part: Anchor breaded Fiesta...
The Issue: Firm used Flour from General Mills that has been contaminated with E. Coli O121.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fire roasted Poblano & Jalapeno popper bites packaged in a Recalled by...
The Issue: Firm used Flour from General Mills that has been contaminated with E. Coli O121.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Viva-ProE Systems Recalled by ELITech Group B.V. Due to Software...
The Issue: Software malfunction; The action being taken due to the device becoming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Radiology Recalled by Mckesson Medical Imaging Group Due to The...
The Issue: The STAT priority icon was not displayed in the Study List when the study...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quattro Air FFM MED AMER Recalled by Resmed Corporation Due to Masks in...
The Issue: Masks in this lot, labelled and sold as 62702 vented Quattro Air FFM size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dextroamphetamine Sulfate Extended-Release Capsules Recalled by Actavis Inc...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Laseredge Knife 1.5mm X 1.7mm TRAPEZOID ANGLED Recalled by Bausch & Lomb Inc...
The Issue: Possible dull knife edge
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laseredge 1.1mm Arrow Knife Angled Recalled by Bausch & Lomb Inc Irb Due to...
The Issue: Possible dull knife edge
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinity Biotech Captia Measles IgM Recalled by Clark Laboratories, Inc....
The Issue: The product lot failed to meet QC acceptance criteria during stability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio PT/INR Test Strips Model Number: 0100071 Recalled by Alere San...
The Issue: Alere San Diego is initiating a voluntary recall for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.