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. 2,102 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,102 in last 12 months

Showing 29813000 of 29,286 recalls

Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard KIT Recalled by AVID Medical, Inc. Due to Foreign Object Contamination

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard SPECIALS PACK - Medical convenience kits Model Number: VAST031-08...

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard CPT PEDS ADULT CH PACK - Medical convenience kits Recalled by AVID...

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard LINE INSERTION PACK - Medical convenience kits Model Number:...

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard SAMMC-N PACEMAKER - Medical convenience kits Model Number:...

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard GYN TRAY - Medical convenience kits Model Number: LANC014-19...

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard C SECTION PACK - Medical convenience kits Model Number: SJCS66-02...

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard ENT - Medical convenience kits Model Number: VMED011-01 Recalled by...

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard PACEMAKER INSTRUMENT PACK - Medical convenience kits Model Number:...

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2024· AVID Medical, Inc.

Recalled Item: Halyard EP TRAY - Medical convenience kits Model Number: VAST038-04 Recalled...

The Issue: Sponge forceps and towel clamps associated with small loose metal flakes...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2024· Ad-Tech Medical Instrument Corporation

Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...

The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2024· Ad-Tech Medical Instrument Corporation

Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...

The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2024· Covidien LP

Recalled Item: Chameleon PTA Balloon Catheter with Injection Port 5mm x 40mm Recalled by...

The Issue: Specific lots of the Chameleon PTA Balloon Catheter failed to meet in-house...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2024· Ad-Tech Medical Instrument Corporation

Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...

The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2024· Nihon Kohden America Inc

Recalled Item: Nihon Kohden Adult Ear Clip SpO2 Sensor Recalled by Nihon Kohden America Inc...

The Issue: Due to oximeters not having FDA market approval or clearance to distribute...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2024· Olympus Corporation of the Americas

Recalled Item: Brand Name: EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190 Product...

The Issue: To better define the drying procedures described in the IFU to improve the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2024· Medtronic Neuromodulation

Recalled Item: Medtronic Recharger Kits Recalled by Medtronic Neuromodulation Due to The...

The Issue: The Wireless Rechargers in the kits may be unable to enter a recharging...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2024· Nihon Kohden America Inc

Recalled Item: Nihon Kohden Adult/Pediatric Forehead Disposable SpO2 Sensor Recalled by...

The Issue: Due to oximeters not having FDA market approval or clearance to distribute...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2024· Baxter Healthcare Corporation

Recalled Item: a. Hillrom Centrella Smart+ Medical-Surgical Hospital Bed Recalled by Baxter...

The Issue: The beds have a potential for an interface issue with the Rauland Responder...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2024· Polymer Technology Systems, Inc. dba PTS Diagnostics, Inc.

Recalled Item: A1CNow+ Multi-Test HbA1c System consists of (1) a semi-disposable...

The Issue: The reason for this recall is PTS Diagnostics, Inc. received complaints of...

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

Class II — Potential Health HazardOngoing