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. 1,110 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
1,110 in last 12 months

Showing 4921–4940 of 29,286 recalls

Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Cefotaxime - 30 ug¿ Recalled by Becton Dickinson & Co. Due...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Cefaclor - 30 ug¿ Recalled by Becton Dickinson & Co. Due...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Minocycline - 30 ug Recalled by Becton Dickinson & Co. Due...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: Sensi Disc Amoxicillin with Clavulanic Acid 20/10 ¿g Recalled by Becton...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Cefpodoxime - 10 ug Recalled by Becton Dickinson & Co. Due...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Rifampin- 5 ug Recalled by Becton Dickinson & Co. Due to...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Azithromycin -15 ¿g Recalled by Becton Dickinson & Co. Due...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Piperacillin/Tazobactam- 100/10 ug Recalled by Becton...

The Issue: There is a possibility of reproducibility, accuracy, and/or QC failures in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2024· Microbiologics Inc

Recalled Item: Microbiologics Enteric Pathogens Control Panel (Inactivated Pellet) Recalled...

The Issue: The negative control was contaminated with one of the positive control...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2024· IMPULSE DYNAMICS (USA) INC

Recalled Item: OPTIMIZER model CCM X11 implantable pulse generator (IPG) devices - Recalled...

The Issue: OPTIMIZER devices may cease to deliver CCM therapy if the device incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Contro-Bulb Syringe Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Packaging material was updated for the Bulb Irrigation Syringe (DYND20125),...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Beckman Coulter, Inc.

Recalled Item: Beckman Coulter DxI 9000 Access Immunoassay Analyzer Recalled by Beckman...

The Issue: A software error caused an increase in tray gripper motion errors that...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Achieva 1.5T. Model (REF) Numbers 781196 Recalled by Philips North America...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Achieva 1.5T Initial system. Model (REF) Numbers 781178. Recalled by Philips...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· United Orthopedic Corporation

Recalled Item: USTAR II Knee System : Cemented Curved Stem Recalled by United Orthopedic...

The Issue: Their is a potential that the implant curved stem may be oriented incorrectly.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· United Orthopedic Corporation

Recalled Item: USTAR II Hip System Press-Fit Curved Stem Recalled by United Orthopedic...

The Issue: Their is a potential that the implant curved stem may be oriented incorrectly.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· United Orthopedic Corporation

Recalled Item: USTAR II Knee System Cemented curved stem Recalled by United Orthopedic...

The Issue: Their is a potential that the implant curved stem may be oriented incorrectly.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Achieva XR. Model (REF) Numbers 781153 Recalled by Philips North America Due...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· FUJIFILM Healthcare Americas Corporation

Recalled Item: Synapse CV 6. with AR. A web-based application as the Recalled by FUJIFILM...

The Issue: The LV Mass (2D Bullet) equation may be calculated incorrectly, resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 3, 2024· Philips North America

Recalled Item: Achieva 3.0T. Model. (REF) Numbers 781277 Recalled by Philips North America...

The Issue: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges...

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

Class II — Potential Health HazardOngoing