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. 2,722 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,722 in last 12 months

Showing 47214740 of 29,286 recalls

Medical DeviceFebruary 7, 2024· Smiths Medical ASD Inc.

Recalled Item: smiths medical Pneupac paraPAC plus 300 ventilator kit without PEEP and CPAP...

The Issue: When a paraPAC plus ventilator is switched to the operating mode of...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 7, 2024· Natus Neurology Inc

Recalled Item: natus neurology Recalled by Natus Neurology Inc Due to Natus has become...

The Issue: Natus has become aware that its third-party supplier Parker Laboratories...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: DCA Systems HbA1c Reagent Kit Recalled by Siemens Healthcare Diagnostics,...

The Issue: The reason for the recall is that the Siemens DCA HbA1c Reagent Kit was...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...

The Issue: Due to two complaints, has come to our attention that additional guidance is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...

The Issue: Due to two complaints, has come to our attention that additional guidance is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...

The Issue: Due to two complaints, has come to our attention that additional guidance is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Waldemar Link GmbH & Co. KG (Mfg Site)

Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...

The Issue: Due to two complaints, has come to our attention that additional guidance is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM Recalled by Howmedica Osteonics...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM Recalled by Howmedica Osteonics...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: X3 TRIATHLON CS INSERT NO 6 10 MM Recalled by Howmedica Osteonics Corp. Due...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: X3 TRIATHLON CS INSERT NO 3 10 MM Recalled by Howmedica Osteonics Corp. Due...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: NO 3 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM Recalled by Howmedica Osteonics...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: X3 TRIATHLON CS INSERT NO 7 9 MM Recalled by Howmedica Osteonics Corp. Due...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: X3 TRIATHLON CS INSERT NO 6 11 MM Recalled by Howmedica Osteonics Corp. Due...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· Howmedica Osteonics Corp.

Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM Recalled by Howmedica Osteonics...

The Issue: Potential packaging breaches of inner blister and outer sterile blister.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 7 with a Certeray generator-To perform image guidance in diagnostic...

The Issue: Generator may fail due to a potential short circuit in the Printed Circuit...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 3 with a Certeray generator -To perform image guidance in diagnostic...

The Issue: Generator may fail due to a potential short circuit in the Printed Circuit...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 5 with a Certeray generator-To perform image guidance in diagnostic...

The Issue: Generator may fail due to a potential short circuit in the Printed Circuit...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2024· Abbott Medical

Recalled Item: Abbott Aveir Leadless Pacemaker Recalled by Abbott Medical Due to Their is a...

The Issue: Their is a potential that electromagnetic interference may cause leadless...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2024· Retractable Technologies, Inc.

Recalled Item: EasyPoint Needle Recalled by Retractable Technologies, Inc. Due to The...

The Issue: The needle cannula of a retractable needle may detach from the needle holder...

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

Class II — Potential Health HazardOngoing