Product Recalls in Nevada

Product recalls affecting Nevada — including food, drugs, consumer products, medical devices, and vehicles distributed to Nevada. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,095 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
1,095 in last 12 months

Showing 8821–8840 of 28,334 recalls

Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Medtronic Neuromodulation

Recalled Item: Medtronic Wireless Recharger Model WR9200 included in the RS6200 Recharger...

The Issue: The wireless rechargers (WR; WR9200 and WR9220; included in the Recharger...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Medtronic Neuromodulation

Recalled Item: Medtronic Wireless Recharger Model WR9200 included in the RS7200 Recharger...

The Issue: The wireless rechargers (WR; WR9200 and WR9220; included in the Recharger...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2021· Leica Microsystems, Inc.

Recalled Item: Leica Microsystems M220 F12 Microscope Systems Recalled by Leica...

The Issue: In May 2021, Leica Microsystems received one (1) complaint pertaining to the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing