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. 1,068 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
1,068 in last 12 months

Showing 11741–11760 of 27,655 recalls

Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· Philips North America, LLC

Recalled Item: Magnetic Resonance Imaging Diagnostic Device accessory - Product Usage: The...

The Issue: The labeling of the Philips Chest Pneumograph does not include a statement...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· American Contract Systems

Recalled Item: Sterile Custom Packs to be used in surgical procedures. Recalled by American...

The Issue: The surgical gowns were manufactured in a facility that is not registered by...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· Philips North America, LLC

Recalled Item: Cardiovascular Monitoring Device accessory - Product Usage: The chest...

The Issue: The labeling of the Philips Chest Pneumograph does not include a statement...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2020· K2M, Inc

Recalled Item: K2M Recalled by K2M, Inc Due to The Aleutian Anatomically Narrow Lordotic...

The Issue: The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2020· Philips North America, LLC

Recalled Item: HeartStart MRx Processor Board PCA Replacement Kits 453563478461 Recalled by...

The Issue: Damaged ESD bags used for storing components in Processor PCA Replacement Kits

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2020· Philips North America, LLC

Recalled Item: Philips Zenition 70 Recalled by Philips North America, LLC Due to When...

The Issue: When strain relief is lost at the stand side of the Stand MVS Trolley Cable,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2020· Philips North America, LLC

Recalled Item: Philips Zenition 50 Recalled by Philips North America, LLC Due to When...

The Issue: When strain relief is lost at the stand side of the Stand MVS Trolley Cable,...

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

Class II — Potential Health HazardOngoing