Product Recalls in North Dakota

Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,535 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,535 in last 12 months

Showing 86818700 of 27,512 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· 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· 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· Wright Medical Technology Inc

Recalled Item: INBONE Total Ankle System Recalled by Wright Medical Technology Inc Due to...

The Issue: The package contents and package labeling do not match.

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· Medtronic Neuromodulation

Recalled Item: Medtronic Wireless Recharger Model WR9220 included in the RS5200 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 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
Medical DeviceNovember 3, 2021· Haag-Streit USA Inc

Recalled Item: OCT-Camera 211 01 A1 Recalled by Haag-Streit USA Inc Due to Malfunction of...

The Issue: Malfunction of the automatic laser beam shut-off, the OCT unit might not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2021· Haag-Streit USA Inc

Recalled Item: OCT-Camera 211 01 A3 Recalled by Haag-Streit USA Inc Due to Malfunction of...

The Issue: Malfunction of the automatic laser beam shut-off, the OCT unit might not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Cardinal Health

Recalled Item: Cardinal Health Poly-Reinforced Surgical Gowns Large SKU: 9010 Recalled by...

The Issue: Potential for open packaging seals compromising the sterility of the...

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

Class II — Potential Health HazardOngoing