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. 2,598 recalls have been distributed to Mississippi in the last 12 months.
Showing 12541–12560 of 28,172 recalls
Recalled Item: BriteBlade Pro Single-Use Fiber Optic Handle and Blade Mac 3 Recalled by...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-se Fiber Optic Miller 2 Recalled by Flexicare Medical...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-Use Fiber Optic Handle and Blade Miller 2 Recalled by...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BriteBlade Pro Single-Use Fiber Optic Mac 3 Recalled by Flexicare Medical...
The Issue: The firm has received reports that the spring/washer/bearing components in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bellavista 1000 ventilator Recalled by Vyaire Medical Due to The G6...
The Issue: The G6 bellavista 1000 US ventilators may experience intermittent failures:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE TUBE Recalled by Greiner Bio-One North America, Inc. Due to The...
The Issue: The Vacuette 3.5mL Serup Sep Clot Activator Tubes may have been damaged at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestation 620/650/650c A2 Product Usage: anesthesia systems are intended...
The Issue: GE Healthcare has become aware that there is a potential for a loose cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestation 620/650/650c A1 Product Usage: anesthesia systems are intended...
The Issue: GE Healthcare has become aware that there is a potential for a loose cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Alpha Recalled by Siemens Medical Solutions USA, Inc Due to During a...
The Issue: During a routine inspection of a system, a crack on the C-arm holder was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOCATOR OVERDENTURE IMPLANT SYSTEM STERILE R Rx Only QTY 1 . Recalled by...
The Issue: The abutment provided with the Implant System may be out of specification,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX Recalled by Radiometer Medical ApS Due to The analyzers fail on...
The Issue: The analyzers fail on S7950 (Range +) QC measurements due to the hemolyzer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX PLUS Recalled by Radiometer Medical ApS Due to The analyzers fail...
The Issue: The analyzers fail on S7950 (Range +) QC measurements due to the hemolyzer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 630G System with SmartGuard Recalled by Medtronic Inc. Due...
The Issue: There have been reported incidents of a loose reservoir that can no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 640G Insulin Infusion Pump Recalled by Medtronic Inc. Due...
The Issue: There have been reported incidents of a loose reservoir that can no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 620G Insulin Infusion Pump Recalled by Medtronic Inc. Due...
The Issue: There have been reported incidents of a loose reservoir that can no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 670G System with SmartGuard Recalled by Medtronic Inc. Due...
The Issue: There have been reported incidents of a loose reservoir that can no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE MODEL: FreeStyle Comfort Oxygen Concentrator - Product Usage: The...
The Issue: Four units of European version FreeStyle Comfort were distributed in the US,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Pin To Rod Coupling External Fixation System Hoffmann II Recalled by...
The Issue: Pin To Rod Coupling could not clamp the pin and rod as intended
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The products involved are DeWALT laser distance measurers Recalled by...
The Issue: The products are labeled as Class II lasers. However, the level of laser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Durapore Advanced Recalled by 3M Company - Health Care Business Due to...
The Issue: While the product meets all safety and efficacy criteria, long term exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.