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. 2,742 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,742 in last 12 months

Showing 10211040 of 29,286 recalls

Medical DeviceSeptember 5, 2025· Spacelabs Healthcare, Inc.

Recalled Item: Brand Name: Branding is not applied to this product. Product Recalled by...

The Issue: Due to display cables used for monitors were not in compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2025· Spacelabs Healthcare, Inc.

Recalled Item: Brand Name: Branding is not applied to this product. Product Recalled by...

The Issue: Due to display cables used for monitors were not in compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2025· MICROVENTION INC.

Recalled Item: Flow Re-Direction Endoluminal Devices: FRED 27 Recalled by MICROVENTION INC....

The Issue: Flow diverter may have a manufacturing issue related to the tantalum length...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2025· GE Medical Systems, SCS

Recalled Item: AW Server 2.0 Recalled by GE Medical Systems, SCS Due to Firm has identified...

The Issue: Firm has identified a security vulnerability in AW Server products. If...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description HSAN63N ANGIO PACK IHAN02W...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description BFCT04X CATARACT PACK -...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description BUCY78E CYSTO PACK CMCP10X...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item number/ Product description AHLD15X LABOR...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits IHDC30R D AND C PACK Recalled by American Contract...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Basic Biopsy Tray Recalled by American Contract Systems Inc. Due to...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description ANSH14AF SHOULDER PACK -...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Basic Biopsy Tray Recalled by American Contract Systems Inc. Due to...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits UDPG88W PICC G-TUBE PACK-230209 Recalled by...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description LKRA40G RADIOLOGY PACK...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description EVLH67F LEFT HEART CATH...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description FHCP08Y C SECTION PK...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· Lutronic Corporation

Recalled Item: XERF EFFECTOR 60. Electrosurgical unit. Recalled by Lutronic Corporation Due...

The Issue: Manufacturing defects in devices manufactured from 4/1/25 to 8/20/25 can on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item number/ Product description AKGN82E GENERAL...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description ANCV78BC HEART PACK -...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· Contego Medical LLC

Recalled Item: Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon Recalled by...

The Issue: Carotid stent and post-dilation balloon system with integrated embolic...

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

Class II — Potential Health HazardOngoing