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. 2,673 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,673 in last 12 months

Showing 92419260 of 29,286 recalls

Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: SmartPath to dStream for 1.5T-a Magnetic Resonance Medical Electrical...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Red Medical Supplies

Recalled Item: EcoGel 200 - RED Medical Supplies Blue Ultrasound Gel Recalled by Red...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 11, 2021· Red Medical Supplies

Recalled Item: EcoGel 200 - RED Medical Supplies Clear Ultrasound Gel Recalled by Red...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 11, 2021· Red Medical Supplies

Recalled Item: EcoGel 100 - RED Medical Supplies Green Ultrasound Gel Recalled by Red...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia 1.5T CX-a Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia Ambition S-a Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia Elition X-a Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Hill-Rom, Inc.

Recalled Item: LikoStretch Mod 600 IC Model Number: 3156065 LikoStretch Mod 600 IC Recalled...

The Issue: Stretch Leveller has the potential to lose the function of maintaining a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Hill-Rom, Inc.

Recalled Item: LikoStretch 1900 Model Number: 3156051 - The combination of this Recalled by...

The Issue: Stretch Leveller has the potential to lose the function of maintaining a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Hill-Rom, Inc.

Recalled Item: FlexoStretch Model Number: 3156057 - The combination of this products...

The Issue: Stretch Leveller has the potential to lose the function of maintaining a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Hill-Rom, Inc.

Recalled Item: OctoStretch with Stretch Leveller - The combination of this products...

The Issue: Stretch Leveller has the potential to lose the function of maintaining a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2021· Philips North America Llc

Recalled Item: Ingenia Ambition X- Magnetic Resonance Medical Electrical Systems indicated...

The Issue: When using manual mode, the tabletop may not completely move in or out and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· ROi CPS LLC

Recalled Item: REGARD Ultrasound Tray Recalled by ROi CPS LLC Due to Povidone-Iodine...

The Issue: Povidone-Iodine swabstick manufactured by PDI, Inc. recalled due to Out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: 10 drops/ml Recalled by B. Braun Medical, Inc. Due to Leakage of the pump...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: Outlook¿ Pump 15 Drop 0.2 Micron Filtered IV Set with Recalled by B. Braun...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: PUMP SET Recalled by B. Braun Medical, Inc. Due to Leakage of the pump set...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT PIN GUIDE KIT R- TruMatch Patient Specific Instruments Recalled...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT CUT GUIDE KIT R- TruMatch Patient Specific Instruments Recalled...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· DePuy Orthopaedics, Inc.

Recalled Item: TRUMATCH CT PIN GUIDE KIT L- TruMatch Patient Specific Instruments Recalled...

The Issue: Software: A coding error associated with the Fast3D Segmentation software....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2021· B. Braun Medical, Inc.

Recalled Item: OUTLOOK PUMP SET Recalled by B. Braun Medical, Inc. Due to Leakage of the...

The Issue: Leakage of the pump set within the cassette portion of the pump sets,...

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

Class II — Potential Health HazardOngoing