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. 2,661 recalls have been distributed to Mississippi in the last 12 months.
Showing 861–880 of 28,172 recalls
Recalled Item: LOW PROF LCKNG SCREW Recalled by Synthes (USA) Products LLC Due to Although...
The Issue: Although the etched length on the screw is correct, the length marked on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cold Form Wrap: Back Recalled by DJO, LLC Due to The IFU (Information for...
The Issue: The IFU (Information for Use) on the wrap instructs the user to heat the hot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm...
The Issue: A manufacturing issue could lead to a malformed cover tube press which can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm...
The Issue: A manufacturing issue could lead to a malformed cover tube press which can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONIC FOCUS Shears + Adaptive Tissue Technology Recalled by Stryker...
The Issue: Due to manufacturing issue, reprocessed shears, may become stuck in the "on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Aesculap Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AESCULAP Product Name: REDUCING CONVERTER 10/12MM TO 5MM...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Aesculap Product Name: SEALING CAP FOR 10/12MM TROCARS Recalled...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AESCULAP Product Name: SEALING UNIT FOR 10/12MM TROCARS Recalled...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Klassic BiPolar Head Model/Catalog Number: 3205.41.022 Klassic...
The Issue: Potential packaging issue that could compromise the sterile barrier. Defect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Veritor Connect Software Recalled by Becton Dickinson & Co. Due to...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD EpiCenter Microbiology Data Management System Recalled by Becton...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC Blood Culture System Recalled by Becton Dickinson & Co. Due to...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC Blood Culture System Recalled by Becton Dickinson & Co. Due to...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MAX System Recalled by Becton Dickinson & Co. Due to Product service...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix M50 Instrument Recalled by Becton Dickinson & Co. Due to Product...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxFLEX Flow Cytometer Catalog Number C78500 UDI-DI code: 15099590754013 The...
The Issue: Due to a software error code that crashes during acquisition on patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Assay: IMMULITE 2000 Intact PTH Recalled by Siemens Healthcare Diagnostics,...
The Issue: The potential for falsely depressed Intact PTH patient results at the low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virata Preassembled Polyaxial Screw Recalled by Orthofix U.S. LLC Due to...
The Issue: Polyaxial screws do not meet performance standards.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...
The Issue: Beckman Coulter has confirmed a software anomaly on DxI 9000 Access...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.