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. 2,455 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,455 in last 12 months

Showing 1572115740 of 27,655 recalls

Medical DeviceApril 20, 2018· Torax Medical, Inc.

Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...

The Issue: Possible out of specification condition which may allow a bead component to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Torax Medical, Inc.

Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...

The Issue: Possible out of specification condition which may allow a bead component to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM go.Now Recalled by Siemens Medical Solutions USA, Inc Due to There...

The Issue: There is a potential for a software issue that may cause the need for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Go.Up Recalled by Siemens Medical Solutions USA, Inc Due to There is...

The Issue: There is a potential for a software issue that may cause the need for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Torax Medical, Inc.

Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...

The Issue: Possible out of specification condition which may allow a bead component to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· Torax Medical, Inc.

Recalled Item: LINX Management System Recalled by Torax Medical, Inc. Due to Possible out...

The Issue: Possible out of specification condition which may allow a bead component to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 20, 2018· CareFusion 303, Inc.

Recalled Item: Alaris Infusion Pump administration sets labeled as: -Infusion Set Alaris...

The Issue: Complaints where users were unable to prime the administration set.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Gentamicin Flex reagent cartridge Recalled by Siemens Healthcare...

The Issue: The affected lots may exhibit inaccuracy for Quality Control and patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Gentamicin Flex reagent cartridge Recalled by Siemens...

The Issue: The affected lots may exhibit inaccuracy for Quality Control and patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2018· MicroAire Surgical Instruments, LLC

Recalled Item: MicroAire SmartRelease Endoscopic System Recalled by MicroAire Surgical...

The Issue: The Instructions for Use (IFU) is incorrect with regards to sterilization...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2018· Maquet SAS

Recalled Item: VOLISTA StandOP (model 600) surgical lights shipped from October 2012...

The Issue: Potential keypad failure on VOLISTA StandOP Surgical Lights.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2018· Gyrus Acmi, Incorporated

Recalled Item: Gyrus ACMI Reusable Active Cord for Bovie/ValleyLab Generators Recalled by...

The Issue: There is a potential for the cord to spark and cause a fire.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2018· Tactical Medical Solutions, Inc.

Recalled Item: BLAST Bandage Recalled by Tactical Medical Solutions, Inc. Due to Blast...

The Issue: Blast Bandages (part# BLAST) with Lot# 0617 were not terminally sterilized.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· Bard Peripheral Vascular Inc

Recalled Item: BARD PERIPHERAL VASCULAR SEEKER(R) Crossing Support Catheter Recalled by...

The Issue: Device is at risk of having detectable levels of bacterial endotoxin present...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Merlin PCS programmer (Model # 3650) Recalled by St Jude Medical Inc. Due to...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Merlin PCS Programmer Software: 3330 The Merlin PCS programmer (model...

The Issue: The firm is advising physicians that exposure to sub-freezing temperatures...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: St. Jude Medical CONFIRM Rx Insertable Cardiac Monitor Recalled by St Jude...

The Issue: The firm is advising physicians that exposure to sub-freezing temperatures...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Quadra Assura Recalled by St Jude Medical Inc. Due to The firm is releasing...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Unify Recalled by St Jude Medical Inc. Due to The firm is releasing new...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Promote Recalled by St Jude Medical Inc. Due to The firm is releasing new...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing