Product Recalls in Idaho
Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,581 recalls have been distributed to Idaho in the last 12 months.
Showing 6881–6900 of 27,833 recalls
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: Irvine Scientific Oil for Embryo Culture (Light Mineral Oil) # 9305 Recalled...
The Issue: Due to the detection of oil toxicity in several lots of Oil for Embryo...
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.
Recalled Item: Atellica IM Folate 700 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: ADVIA Centaur Folate 500 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 500 test kit- 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.