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. 2,716 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,716 in last 12 months

Showing 58615880 of 29,286 recalls

Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: EVIS EXERA III DUODENOVIDEOSCOPE OLYMPUS TJF-Q190V Recalled by Olympus...

The Issue: Recent reports of patient infection.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Bronchovideoscope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Airway Mobilescope Recalled by Olympus Corporation of the Americas...

The Issue: Complaint of endoscope model becoming lodged in the endotracheal tube...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-MR1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-C1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton C1/T1/MR1 Recalled by Hamilton Medical, Inc. Due to Degrading...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-T1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-T1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Hamilton Medical, Inc.

Recalled Item: Hamilton-T1 Recalled by Hamilton Medical, Inc. Due to Degrading capacitors...

The Issue: Degrading capacitors on the control board of ventilators and spare parts may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 26, 2023· Zimmer, Inc.

Recalled Item: M/L Taper Hip Prosthesis Extended Offset Recalled by Zimmer, Inc. Due to The...

The Issue: The outer package labeling and product etch are for a Size 6, however, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2023· SenTec AG

Recalled Item: Membrane Changer Single-Use Recalled by SenTec AG Due to During rework of...

The Issue: During rework of components during the manufacturing process, an additional...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2023· Diversatek Healthcare

Recalled Item: ZVU Functional GI Software Recalled by Diversatek Healthcare Due to GI...

The Issue: GI Software labelled as revision 3.3.0 is incorrectly labeled and is in fact...

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

Class III — Low RiskOngoing
Medical DeviceJuly 25, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by...

The Issue: There is a potential for ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2023· Medtronic Navigation, Inc.-Littleton

Recalled Item: The O-arm O2 Imaging System is a mobile x-ray system Recalled by Medtronic...

The Issue: Ground cable installed incorrectly.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2023· Cook Vandergrift, Inc.

Recalled Item: Cook Lead Clipper- An auxiliary tool indicated for use in Recalled by Cook...

The Issue: Sterility of device may be compromised due to breach of the chevron seal of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2023· Ambu Inc.

Recalled Item: Ambu aView 2 A Monitor-The Ambu aView 2 Advance is Recalled by Ambu Inc. Due...

The Issue: Multiple impacts, for example from being dropped, can cause to the Ambu...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2023· Keystone Industries

Recalled Item: Keystone Bosworth Copaliner Cavity Varnish .5oz (14 ml)- Intended to...

The Issue: A bottle of Copaliner Solvent was inadvertently packaged into a box labeled...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2023· Philips Medical Systems Nederland B.V.

Recalled Item: Zenition 70. The device is to be used in health Recalled by Philips Medical...

The Issue: Philips has become aware of the potential for unintended radiation exposure...

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

Class II — Potential Health HazardOngoing