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 44814500 of 29,286 recalls

Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: GYROSCAN ACS-NT Recalled by Philips North America Llc Due to Patient support...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Achieva XR Recalled by Philips North America Llc Due to Patient support...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Intera 1.5T Achieva Nova-Dual Recalled by Philips North America Llc Due to...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Ingenia 1.5T CX Recalled by Philips North America Llc Due to Patient support...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Intera 0.5T Standard Recalled by Philips North America Llc Due to Patient...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Intera 1.5T Power/Pulsar Recalled by Philips North America Llc Due to...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Achieva 3.0TX for PET Recalled by Philips North America Llc Due to Patient...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: GYROSCAN T5 Recalled by Philips North America Llc Due to Patient support...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Achieva 3.0T Recalled by Philips North America Llc Due to Patient support...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Intera Achieva 1.5T Pulsar Recalled by Philips North America Llc Due to...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Namic FLUID DELIVERY SET Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Products have a lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: namic CONVENIENCE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Products have a lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Achieva 1.5T Initial Recalled by Philips North America Llc Due to Patient...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: Intera 1.5T R11 Recalled by Philips North America Llc Due to Patient support...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 12, 2024· Philips North America Llc

Recalled Item: MR 7700 Recalled by Philips North America Llc Due to Patient support table...

The Issue: Patient support table floor plate may be incorrectly installed.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2024· Advanced Instruments, LLC

Recalled Item: OsmoPRO MAX Automated Osmometer- IVD Osmometer for Clinical Use. Uses...

The Issue: System error messages may delay the ability to test patient samples and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2024· Baxter Healthcare Corporation

Recalled Item: HDS Traction Boot II Recalled by Baxter Healthcare Corporation Due to Baxter...

The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2024· Conformis, Inc.

Recalled Item: Identity Imprint PS Tibial Tray Size 4: Lot 540287 Recalled by Conformis,...

The Issue: Size 5 Tibial Tray from Lot 508287 was packaged in a Size 4 box from Lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2024· Smith & Nephew Medical, Ltd.

Recalled Item: RENASYS EDGE 300ML CANISTER WITH Solidifier- Indicated for patients who...

The Issue: Black particulate matter from the carbon filter component of the canisters...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2024· Smith & Nephew Medical, Ltd.

Recalled Item: RENASYS EDGE 800ML CANISTER WITH Solidifier- Indicated for patients who...

The Issue: Black particulate matter from the carbon filter component of the canisters...

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

Class II — Potential Health HazardOngoing