Product Recalls in Minnesota

Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,654 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,654 in last 12 months

Showing 92219240 of 29,186 recalls

Medical DeviceAugust 13, 2021· Philips North America Llc

Recalled Item: The Azurion series (within the limits of the used Operation Recalled by...

The Issue: Early life failure of the ADUs only occurs when the hospital mains provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2021· Quidel Corporation

Recalled Item: Lyra Direct SARS-CoV-2 Assay Emergency Use Authorization- . The Recalled by...

The Issue: Revised Instructions for Use: Potential for specimens from patients with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2021· Philips North America Llc

Recalled Item: The Allura Xper series is intended for use on human Recalled by Philips...

The Issue: Early life failure of the ADUs only occurs when the hospital mains provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2021· AMTEC SALES Inc

Recalled Item: EcoGel 100 Imaging Gel Recalled by AMTEC SALES Inc Due to Ultrasound gels...

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 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· 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: Stretch Leveller Model Number: 3156200 - 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 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· 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 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 1.5T- a Magnetic Resonance Medical Electrical Systems indicated for...

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: SmartPath to dStream for XR and 3.0T-a Magnetic Resonance Medical Recalled...

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 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 11, 2021· Philips North America Llc

Recalled Item: Ingenia 3.0T 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 1.5T Evolution-a Magnetic Resonance Medical Electrical Systems...

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