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. 1,061 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,061 in last 12 months

Showing 6641–6660 of 27,512 recalls

Medical DeviceMarch 1, 2023· Stryker Corporation

Recalled Item: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 18X4...

The Issue: Not able to achieve desired pressure and not holding pressure result from...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Covidien, LP

Recalled Item: Mild Chromic Gut Absorbable Sutures Recalled by Covidien, LP Due to...

The Issue: Medtronic was made aware of a supplier calibration issue during the contract...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Terumo Cardiovascular Systems Corporation

Recalled Item: CAPIOX RX15 Hollow Fiber Oxygenator Recalled by Terumo Cardiovascular...

The Issue: Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Coloplast Manufacturing US, LLC

Recalled Item: Titan Touch Scro Zero Ang 16cm Recalled by Coloplast Manufacturing US, LLC...

The Issue: A decrease in wall thickness has the potential for a premature pump failure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Terumo Cardiovascular Systems Corporation

Recalled Item: CAPIOX FX25 Hollow Fiber Oxygenator Recalled by Terumo Cardiovascular...

The Issue: Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Stryker Corporation

Recalled Item: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 18X4...

The Issue: Not able to achieve desired pressure and not holding pressure result from...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Coloplast Manufacturing US, LLC

Recalled Item: Titan 0-Deg Infrapubic 20 Cm Recalled by Coloplast Manufacturing US, LLC Due...

The Issue: A decrease in wall thickness has the potential for a premature pump failure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Coloplast Manufacturing US, LLC

Recalled Item: Titan Touch NB Scrot Zero 16cm Recalled by Coloplast Manufacturing US, LLC...

The Issue: A decrease in wall thickness has the potential for a premature pump failure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Philips Respironics, Inc.

Recalled Item: Trilogy Evo O2 and LifeVentEVO2 Portable Electric Ventilator Recalled by...

The Issue: The accuracy of delivered oxygen may deviate below the required tolerance of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2023· Coloplast Manufacturing US, LLC

Recalled Item: Titan Touch NB Infr Zero 16cm Recalled by Coloplast Manufacturing US, LLC...

The Issue: A decrease in wall thickness has the potential for a premature pump failure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Covidien, LP

Recalled Item: Chromic Gut Absorbable Sutures Recalled by Covidien, LP Due to Medtronic was...

The Issue: Medtronic was made aware of a supplier calibration issue during the contract...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Coloplast Manufacturing US, LLC

Recalled Item: Titan 0-Deg Scrotal 18 Cm Recalled by Coloplast Manufacturing US, LLC Due to...

The Issue: A decrease in wall thickness has the potential for a premature pump failure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Coloplast Manufacturing US, LLC

Recalled Item: Titan NB Scrotal Zero Ang 18cm Recalled by Coloplast Manufacturing US, LLC...

The Issue: A decrease in wall thickness has the potential for a premature pump failure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Stryker Corporation

Recalled Item: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 34X4...

The Issue: Not able to achieve desired pressure and not holding pressure result from...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Coloplast Manufacturing US, LLC

Recalled Item: Titan Touch Scro Zero Ang 20cm Recalled by Coloplast Manufacturing US, LLC...

The Issue: A decrease in wall thickness has the potential for a premature pump failure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Coloplast Manufacturing US, LLC

Recalled Item: Titan Touch Scro Zero Ang 22cm Recalled by Coloplast Manufacturing US, LLC...

The Issue: A decrease in wall thickness has the potential for a premature pump failure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Universal Portable Electric Ventilator Recalled by Philips...

The Issue: The accuracy of delivered oxygen may deviate below the required tolerance of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2023· Coloplast Manufacturing US, LLC

Recalled Item: Titan 0-Deg Scrotal 20 Cm Recalled by Coloplast Manufacturing US, LLC Due to XXX

The Issue: XXX

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: Shanghai United Imaging Healthcare Co. Recalled by Shanghai United Imaging...

The Issue: Due to a software issue where the process of patient scanning, the scatter...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2023· Terumo Cardiovascular Systems Corporation

Recalled Item: CAPIOX NX19 Hollow Fiber Oxygenator Recalled by Terumo Cardiovascular...

The Issue: Some Capiox NX, RX and FX Oxygenators may contain an arterial thermistor...

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

Class II — Potential Health HazardOngoing