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. 1,057 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
1,057 in last 12 months

Showing 16981–17000 of 53,342 recalls

Medical DeviceFebruary 9, 2021· Philips North America LLC

Recalled Item: Philips Recalled by Philips North America LLC Due to Customers were not...

The Issue: Customers were not notified of previous recalls associated with various...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2021· Philips North America LLC

Recalled Item: Philips Recalled by Philips North America LLC Due to Customers were not...

The Issue: Customers were not notified of previous recalls associated with various...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2021· Meridian Bioscience Inc

Recalled Item: The ImmunoCard Mycoplasma EIA detects the presence of IgM to Recalled by...

The Issue: Use of the kits after incorrect storage could lead to a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2021· Mizuho OSI

Recalled Item: Mizuho CE IPX4 Recalled by Mizuho OSI Due to There is a potential that hand...

The Issue: There is a potential that hand control units may cause the tabletop to slide...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2021· Sharp Medical Products

Recalled Item: SHARP MEDICAL PRODUCTS Recalled by Sharp Medical Products Due to...

The Issue: Non-conformity (holes/punctures or deep creases) in the sterile barrier.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2021· GE Healthcare, LLC

Recalled Item: NM/CT 850 Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC Due...

The Issue: GE Healthcare has become aware of a potential issue on 800 family NM/CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2021· GE Healthcare, LLC

Recalled Item: NM/CT 860 Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC Due...

The Issue: GE Healthcare has become aware of a potential issue on 800 family NM/CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 7, 2021· GE Healthcare, LLC

Recalled Item: NM/CT 870 DR Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC...

The Issue: GE Healthcare has become aware of a potential issue on 800 family NM/CT...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2021· Canon Medical System, USA, INC.

Recalled Item: System INFX-8000F Recalled by Canon Medical System, USA, INC. Due to The...

The Issue: The x-ray irradiation field may shift with respect to image receiving...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2021· Canon Medical System, USA, INC.

Recalled Item: System INFX-8000C Recalled by Canon Medical System, USA, INC. Due to The...

The Issue: The x-ray irradiation field may shift with respect to image receiving...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2021· Canon Medical System, USA, INC.

Recalled Item: System INFX-8000V Recalled by Canon Medical System, USA, INC. Due to The...

The Issue: The x-ray irradiation field may shift with respect to image receiving...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2021· OraSure Technologies, Inc.

Recalled Item: Methamphetamine Intercept Microplate kit EIA - IVD qualitative determination...

The Issue: Incorrect lot of Substrate Reagent (TMB) may be included in the kit. The...

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

Class III — Low RiskOngoing
DrugFebruary 5, 2021· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Pantoprazole Sodium for Injection 40mg/vial For I.V. infusion only...

The Issue: Failed Impurity/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodFebruary 5, 2021· Shenandoah Growers, Inc.

Recalled Item: Organic fresh cut basil packaged in plastic clamshell containers. Shenandoah...

The Issue: Possible contamination with Cyclospora in basil

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic Custom Pack CP Kinderset 1/4-1/4 MIT Pixie 1/B (PERFUSION Recalled...

The Issue: Products being recalled due to potentially elevated level of bacterial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic Custom Pack Infant Tubingset Pixie Flow 0 Recalled by Medtronic...

The Issue: Products being recalled due to potentially elevated level of bacterial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Custom Perfusion System (CUSTOM PACK BB7W03R8 CCSM NEON). The Affinity...

The Issue: Products being recalled due to potentially elevated level of bacterial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Siemens Medical Solutions USA, Inc.

Recalled Item: Product Label - ACUSON Sequoia *** Power Input: 100-240V~ Recalled by...

The Issue: The ultrasound system averages the Mean Sac Diameter (MSD) and Gestational...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Custom Perfusion System (CUSTOM PACK HY10J00R6 ECC SMALL CAR). The Recalled...

The Issue: Products being recalled due to potentially elevated level of bacterial...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 4, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic Custom Pack EVNP Clinical with AP40 1/B (PERFUSION M448036B...

The Issue: Products being recalled due to potentially elevated level of bacterial...

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

Class I — Serious Health HazardOngoing