Product Recalls in Maine

Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,520 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,520 in last 12 months

Showing 95019520 of 27,655 recalls

Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft may go unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2021· Sentinel CH SpA

Recalled Item: ACE Control Set - IVD Control set for the quantitative Recalled by Sentinel...

The Issue: Claim for stability after reconstitution from lyophilized to liquid form...

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

Class III — Low RiskOngoing
Medical DeviceApril 30, 2021· Nico Corp.

Recalled Item: Myriad-LX Light Source-for delivery of light to the surgical field Recalled...

The Issue: (1) Updated IFU for the LX Illumination Packs: Warning - Avoid contact...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2021· Nico Corp.

Recalled Item: NICO Myriad-LX Illumination Pack: Mvriad-LX Illumination Pack. 11ga Recalled...

The Issue: (1) Updated IFU for the LX Illumination Packs: Warning - Avoid contact...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2021· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Synapse Cardiovascular (Synapse CV). Software Versions: 6.0 to 6.2.1 The...

The Issue: Software versions 6.0.4 to 6.2.1 using Advanced Reporting -possibility that...

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

Class II — Potential Health HazardOngoing