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. 967 recalls have been distributed to Mississippi in the last 12 months.
Showing 40801–40820 of 49,744 recalls
Recalled Item: External power supply adaptors that accompany Clinitek Status+ The Clinitek...
The Issue: The external power supply for the Clintek Status analyzer, which is provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: External power supply adaptors that accompany Clinitek Status Connect System...
The Issue: The external power supply for the Clintek Status analyzer, which is provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE /IMMULITE 1000 Systems COR Cortisol Recalled by Siemens Healthcare...
The Issue: Customer complaints were received for positive bias reported on the controls...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carescape Patient Data Module Recalled by GE Healthcare, LLC...
The Issue: GE Healthcare has recently become aware of a potential safety issue to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: External power supply adaptors that accompany Clinitek Status Power Supply...
The Issue: The external power supply for the Clintek Status analyzer, which is provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mars Chocolate North America Milk Chocolate M & M's Net Recalled by Mars...
The Issue: Mars Chocolate North America is recalling M & Ms due to undeclared peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: E-Z- GAS II EFFERVESCENT GRANULES Antacid/Antiflatulent Recalled by Bracco...
The Issue: Subpotent Drug: Out of Specification (OOS) result during routine stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Covidien Kendall Adult Multi-Function Defibrillation Electrodes Part Number:...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoWrist Stapler 45 instrument for the da Vinci Si System Recalled by...
The Issue: Intuitive is issuing an urgent product notice to all users of the EndoWrist...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number:...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Medi-Trace Cadence and Kendall Adult Multi-Function Defibrillation...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coviden Medi-Trace Cadence Adult Multi-Function Defibrillation Electrodes...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HEARTSTART Multifunction Electrode Pads Part Number: M3718A Recalled...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice¿ Multifunction Electrode Part Number: MC171 OH Recalled by...
The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Richard-Allan Scientific 10% Neutral Buffered Formalin. Product Usage: 10%...
The Issue: The affected lots could have NBF concentrations that are lower or higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Richard-Allan Scientific Bio-Tite Specimen Containers. Product Usage: 10%...
The Issue: The affected lots could have NBF concentrations that are lower or higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Richard-Allan Scientific 10% Neutral Buffered Formalin. Product Usage: 10%...
The Issue: The affected lots could have NBF concentrations that are lower or higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Protocol 10% NBF Product Usage: 10% NBF is used to Recalled by Richard-Allan...
The Issue: The affected lots could have NBF concentrations that are lower or higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Richard-Allan Scientific Specimen Transportation System. Product Usage: 10%...
The Issue: The affected lots could have NBF concentrations that are lower or higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EndoWrist One Vessel Sealer used in conjunction with the da Recalled by...
The Issue: Intuitive Surgical is initiating a voluntary correction relating to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.