Product Recalls in Michigan

Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,707 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,707 in last 12 months

Showing 68016820 of 29,286 recalls

Medical DeviceMarch 1, 2023· Coloplast Manufacturing US, LLC

Recalled Item: Titan Touch NB Infr Zero 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· 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 Touch Pump Recalled by Coloplast Manufacturing US, LLC Due to A...

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 Infra Zero Ang 16cm 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· 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
Medical DeviceMarch 1, 2023· Stryker Corporation

Recalled Item: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 30X4...

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· Stryker Corporation

Recalled Item: Stryker Color Cuff Non-Sterile Disposable Tourniquet Cuff -NS DISP 30X4...

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· 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· 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· 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· Philips Respironics, Inc.

Recalled Item: Trilogy EV300 Portable Electric Ventilator Recalled by Philips Respironics,...

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· 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· 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· 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· 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· 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· Elekta Instrument AB

Recalled Item: Instructions for Use for the following Leksell Stereotactic System and...

The Issue: The incorrect IFU was distributed with the devices.

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

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

Recalled Item: Express Mini 500 Dry Seal Chest Drain Recalled by Atrium Medical Corporation...

The Issue: The Instructions for Use (IFU) for the Pneumostat Chest Drain Valve and the...

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

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

Recalled Item: Color Cuff Single Port Recalled by Stryker Sustainability Solutions Due to...

The Issue: Increased incidence of disposable tourniquet cuffs "not able to achieve...

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

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

Recalled Item: Atrium Pneumostat Chest Drain Valve Recalled by Atrium Medical Corporation...

The Issue: The Instructions for Use (IFU) for the Pneumostat Chest Drain Valve and the...

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

Class II — Potential Health HazardOngoing