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. 2,645 recalls have been distributed to Mississippi in the last 12 months.
Showing 3741–3760 of 28,172 recalls
Recalled Item: QIAcube Connect MDx - IVD Instrument designed to perform automated Recalled...
The Issue: Heater shaker module does not perform heating if the temperature is set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RTL190395: 2008K@HOME MACHINE Recalled by Fresenius Medical Care Holdings,...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RTLR190395: 2008K@HOME MACHINE Recalled by Fresenius Medical Care Holdings,...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 190904 2008K@HOME HEMODIALYSIS SYSTEM W/ BIBAG - Blood Pump Rotor spare part...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 190395: 2008K@HOME MACHINE Recalled by Fresenius Medical Care Holdings, Inc....
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 190828: 2008K@HOME HEMODIALYSIS SYSTEM - Blood Pump Rotor spare part...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RTL190904: 2008K@HOME HEMODIALYSIS SYSTEM W/ BIBAG - Blood Pump Rotor spare...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 191014: 2008K@HOME HD SYSTEM W/BIBAG (CANADA) - Blood Pump Rotor spare part...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RTL190828: 2008K@HOME HEMODIALYSIS SYSTEM - Blood Pump Rotor spare part...
The Issue: An increased number of complaints were reported on the Blood Pump Rotor (P/N...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Non-Sterile Flyte hood covers the user s head and Recalled by Stryker...
The Issue: Expired Products distributed to customers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neurostimulation Kit (Ported Recalled by Nalu Medical, Inc. Due to...
The Issue: Neurostimulation Systems have a manufacturing non-conformance that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This product is a single use sterile device that is Recalled by Stryker...
The Issue: Expired Products distributed to customers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Curved Recalled by Stryker Corporation Due to Expired Products distributed...
The Issue: Expired Products distributed to customers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Kittner Blunt Dissecting Instrument Recalled by ASPEN SURGICAL...
The Issue: The affected products may have been packaged with a defect in the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nanoplasty 3D Bunion Correction System Implant Recalled by Treace Medical...
The Issue: Potential issue causing a higher frequency of interference with locking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIC-KEY* Gastric-Jejunal Feeding Tube Kit Recalled by Avanos Medical, Inc....
The Issue: The IFU was missing some risk information requested by another country to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive Premium SuperPulsed Laser System Recalled by Olympus Corporation of...
The Issue: Difficulties in pairing the wireless footswitch with the Soltive Laser,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive Pro SuperPulsed Laser System Recalled by Olympus Corporation of the...
The Issue: Difficulties in pairing the wireless footswitch with the Soltive Laser,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soltive SuperPulsed Laser System Wireless Footswitch Recalled by Olympus...
The Issue: Difficulties in pairing the wireless footswitch with the Soltive Laser,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL800 FLEX Model Numbers 393-800 and 393-801 The ABL800 FLEX Recalled by...
The Issue: Issue with analyzer when the pH of the calibration solution decreases during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.