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. 2,628 recalls have been distributed to Mississippi in the last 12 months.
Showing 6861–6880 of 28,172 recalls
Recalled Item: Outset Tablo Model Numbers (REF): PN-0006000 PN-0007001 Tablo is a Recalled...
The Issue: An observed trend of high conductivity dialysate alarms in a hemodialysis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Side Cart Recalled by Intuitive Surgical, Inc. Due to Preventative...
The Issue: Preventative maintenance data was used to identify instrument Arms, part of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network...
The Issue: Infusion pump PCs with specific software/network cards/IP addresses can have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaStar TS Recalled by Draeger Medical, Inc. Due to The magnets used in the...
The Issue: The magnets used in the swivel frame/tube set and the headgear clips might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaStar TS Recalled by Draeger Medical, Inc. Due to The magnets used in the...
The Issue: The magnets used in the swivel frame/tube set and the headgear clips might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surepulse VS Cap Large component of VS Newborn Recalled by SUREPULSE MEDICAL...
The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surepulse VS Cap Medium component of VS Newborn Recalled by SUREPULSE...
The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surepulse VS Cap Small component of VS Newborn Recalled by SUREPULSE MEDICAL...
The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surepulse VS Cap Extra Small component of VS Recalled by SUREPULSE MEDICAL...
The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surepulse VS Cap Extra Large component of VS Recalled by SUREPULSE MEDICAL...
The Issue: Retroactively reported; Labeling contains incorrect sizing guide for Cap, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SenSight Connector Plug Recalled by Medtronic Neuromodulation Due to...
The Issue: Medtronic is requesting return of a small number of units of the SenSight...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SciCan STATIS SL S10001 Dental Handpieces-Intended for the removal of...
The Issue: Screw connection between the turbine head and the push button may loosen and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue G7m Anesthesia Gas Module Recalled by Philips North America Due...
The Issue: The 866173 lntelliVue G7m Anesthesia Gas Modules could have a component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hologic 3Dimensions/Selenia Dimensions Models: RM-SDM-00001-3D SDM-00001-2D...
The Issue: C-Arm unexpected movement may cause blunt trauma should the tube arm impinge...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Biograph mCT: a) Flow 64-4R Seismic Recalled by Siemens Medical...
The Issue: This is a potential problem with the locking mechanism that is used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Biograph Vision: a) 450 Recalled by Siemens Medical Solutions USA,...
The Issue: This is a potential problem with the locking mechanism that is used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Biograph Horizon 3R Mobile Recalled by Siemens Medical Solutions...
The Issue: This is a potential problem with the locking mechanism that is used to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Folate 140 test kit- For in vitro diagnostic Recalled by Siemens...
The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Folate 700 test kit (REF)-For in vitro diagnostic Recalled by...
The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Folate 100 test kit-For in vitro diagnostic use Recalled by...
The Issue: Negative bias occurred when whole blood calibration (Atellica IM Fol or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.