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. 2,576 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,576 in last 12 months

Showing 1646116480 of 29,286 recalls

Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee biplane MN Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zeego Recalled by Siemens Medical Solutions USA, Inc Due to After the...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Philips Medical Systems Nederlands

Recalled Item: OmniDiagnost-Eleva X-ray system Angiographic and Diagnostic Recalled by...

The Issue: The fixation of the upper and lower tilt actuator, of the Omnidiagnost...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee MP Recalled by Siemens Medical Solutions USA, Inc Due to After the...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee biplane Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Philips Medical Systems Nederlands

Recalled Item: OmniDiagnost Classic X-ray system Angiographic and Diagnostic Recalled by...

The Issue: The fixation of the upper and lower tilt actuator, of the Omnidiagnost...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee ceiling Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee floor Recalled by Siemens Medical Solutions USA, Inc Due to After...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen biplane Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee floor MN Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· TP Orthodontics, Inc.

Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...

The Issue: The firm has received 106 complaints of the device breaking in the patient's...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· TP Orthodontics, Inc.

Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...

The Issue: The firm has received 106 complaints of the device breaking in the patient's...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· TP Orthodontics, Inc.

Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...

The Issue: The firm has received 106 complaints of the device breaking in the patient's...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· TP Orthodontics, Inc.

Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...

The Issue: The firm has received 106 complaints of the device breaking in the patient's...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· TP Orthodontics, Inc.

Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...

The Issue: The firm has received 106 complaints of the device breaking in the patient's...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· TP Orthodontics, Inc.

Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...

The Issue: The firm has received 106 complaints of the device breaking in the patient's...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· TP Orthodontics, Inc.

Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...

The Issue: The firm has received 106 complaints of the device breaking in the patient's...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· TP Orthodontics, Inc.

Recalled Item: Jasper Vektor Recalled by TP Orthodontics, Inc. Due to The firm has received...

The Issue: The firm has received 106 complaints of the device breaking in the patient's...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2018· Philips Electronics North America Corporation

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...

The Issue: Five warning statements are missing from the instructions for use.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2018· Philips Electronics North America Corporation

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...

The Issue: Five warning statements are missing from the instructions for use.

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

Class II — Potential Health HazardOngoing