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 58815900 of 29,286 recalls

Medical DeviceJuly 20, 2023· Cosmedent, Inc.

Recalled Item: Cosmedent FlexiCup Composite Finishing & Polishing System Recalled by...

The Issue: Reports were received the elastomer cup material is crumbling.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2023· Aesculap Implant Systems LLC

Recalled Item: For intraventricular indications mainly used for operations within the brain...

The Issue: Trocar manufactured with the shaft too long and does not meet manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2023· Olympus Corporation of the Americas

Recalled Item: Visera Hysterovideoscope Olympus HYF Type V Recalled by Olympus Corporation...

The Issue: IFU labeling is being updated to revise EtO gas mixture and elimination of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2023· Reichert, Inc.

Recalled Item: PHOROPTOR VRX DIGITAL SYSTEM-Digital intended for the subjective Recalled by...

The Issue: Phoroptor VRx Head may detach from the bracket that connects the Phoroptor...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2023· NOXBOX LTD

Recalled Item: NOxBOXi Nitric Oxide Delivery System Recalled by NOXBOX LTD Due to...

The Issue: Replacement of the internal Sample Pump due to high failure rates.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2023· IHB OPERATIONS B.V.

Recalled Item: Freedom Boom models series: F110 Recalled by IHB OPERATIONS B.V. Due to...

The Issue: Weakened connection point on the adjustable suspension arm, potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2023· Philips Medical Systems Nederland B.V.

Recalled Item: Allura Xper series Recalled by Philips Medical Systems Nederland B.V. Due to...

The Issue: A foot switch pedal may get stuck in the active position when the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2023· Philips Medical Systems Nederland B.V.

Recalled Item: Azurion Recalled by Philips Medical Systems Nederland B.V. Due to A foot...

The Issue: A foot switch pedal may get stuck in the active position when the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2023· Philips Medical Systems Nederland B.V.

Recalled Item: MultiDiagnost-Eleva Recalled by Philips Medical Systems Nederland B.V. Due...

The Issue: A foot switch pedal may get stuck in the active position when the user...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2023· Randox Laboratories Ltd.

Recalled Item: Randox Liquid Protein Calibrators-SP CAL-(LIQ)-In vitro diagnostic product...

The Issue: As part of the firm's ongoing quality monitoring (see internal complaint #...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2023· Abbott Medical

Recalled Item: Proclaim" XR 7 Implantable Pulse Generator (previously known Recalled by...

The Issue: Firm has received complaints from patients who are unable to exit MRI...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2023· Abbott Medical

Recalled Item: Proclaim Plus 5 Implantable Pulse Generator Product Description: Recalled by...

The Issue: Firm has received complaints from patients who are unable to exit MRI...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2023· Abbott Medical

Recalled Item: Proclaim XR 5 Implantable Pulse Genterator (previously known Recalled by...

The Issue: Firm has received complaints from patients who are unable to exit MRI...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2023· Abbott Medical

Recalled Item: Infinity 5 Implantable Pulse Generator Product Description: The Recalled by...

The Issue: Firm has received complaints from patients who are unable to exit MRI...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2023· Abbott Medical

Recalled Item: Infinity 7 Implantable Pulse Generator Product Description: The Recalled by...

The Issue: Firm has received complaints from patients who are unable to exit MRI...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2023· Abbott Medical

Recalled Item: Proclaim DRG Implantable Pulse Generator Product Description: The Recalled...

The Issue: Firm has received complaints from patients who are unable to exit MRI...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2023· Abbott Medical

Recalled Item: Proclaim Plus 7 Implantable Pulse Generator Product Description: Recalled by...

The Issue: Firm has received complaints from patients who are unable to exit MRI...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2023· Smiths Medical ASD Inc.

Recalled Item: PORTEX 0.5u HYDROPHOBIC DISC FILTER Recalled by Smiths Medical ASD Inc. Due...

The Issue: Smiths Medical identified a labeling error in which the barcode (UDI) was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2023· WOM World Of Medicine AG

Recalled Item: Aquilex Fluid Control System-Intended to provide fluid distension of the...

The Issue: The display of inflow volume can reach its limit of 30,000 ml during long...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2023· RAYSEARCH LABORATORIES AB

Recalled Item: RayCare software Recalled by RAYSEARCH LABORATORIES AB Due to An issue was...

The Issue: An issue was found in Software RayCare 5A, 5B, 6A, including service packs,...

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

Class II — Potential Health HazardOngoing