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. 2,623 recalls have been distributed to Mississippi in the last 12 months.
Showing 8861–8880 of 28,172 recalls
Recalled Item: Medtronic Custom Perfusion kits Recalled by Medtronic Perfusion Systems Due...
The Issue: Product is labeled as non-pyrogenic but endotoxin testing was not performed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis pheno with software VE20C- diagnostic imaging angiography system...
The Issue: Four potential software issues with Artis pheno and Artis icono systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono biplane with software VE20C-diagnostic imaging angiography...
The Issue: Four potential software issues with Artis pheno and Artis icono systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono floor with software VE20C-diagnostic imaging angiography system...
The Issue: Four potential software issues with Artis pheno and Artis icono systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CareLink SmartSync Device Manager application software (D00U005)...
The Issue: The processing of collected episode data may fail due to a software error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affected components are limited to the Monoprice charging cable (Product...
The Issue: Warning Added: Using damaged cables or chargers, or charging when moisture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFire Blood Culture Identification 2 (BCID2) Panel Part No: RFIT-ASY-0147...
The Issue: Due to an increased risk of false positive Acinetobacter calcoaceticus-...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GM Helix Acqua Implant 3.5x10 Recalled by Jjgc Industria E Comercio De...
The Issue: 3.5x11.5mm implants were mislabeled as 3.5x10mm implants. In borderline...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VirtuTRAX Instrument Navigator Recalled by Civco Medical Instruments Co....
The Issue: There is potential that the VirtuTRAX device will not tighten onto the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VirtuTRAX Instrument Navigator Recalled by Civco Medical Instruments Co....
The Issue: There is potential that the VirtuTRAX device will not tighten onto the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VirtuTRAX Instrument Navigator Recalled by Civco Medical Instruments Co....
The Issue: There is potential that the VirtuTRAX device will not tighten onto the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VirtuTRAX Instrument Navigator Recalled by Civco Medical Instruments Co....
The Issue: There is potential that the VirtuTRAX device will not tighten onto the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transseptal Needle with Catheter. RPN TSN-17-75.0-ENDRYS. GPN G19261....
The Issue: Transseptal needles may contain rust on the interior and/or exterior of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi CustomEyes Kit-Lafayette General Medical Center: CustomEyes Cataract...
The Issue: Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beaver Xstar Crescent Knife Recalled by Beaver Visitec International, Inc....
The Issue: Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi CustomEyes Kit-CustomEyes Cataract Surgical Kits that contain Beaver...
The Issue: Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transseptal Needle Recalled by Cook Inc. Due to Transseptal needles may...
The Issue: Transseptal needles may contain rust on the interior and/or exterior of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi CustomEyes Kit-AMO Germany GmbH Katarakt-set - Dr. Wagner: CustomEyes...
The Issue: Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ComposiTCP 30 Interference screw D 7- L:25 mm Recalled by SCIENCE & BIO...
The Issue: Mislabeled product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Red Dot Electrodes Recalled by 3M Company - Health Care Business Due to...
The Issue: Potential for breakage of the ECG electrode carbon stud from the eyelet.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.