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. 2,546 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,546 in last 12 months

Showing 43214340 of 27,655 recalls

Medical DeviceMarch 19, 2024· TriMed Inc.

Recalled Item: TriMed Recalled by TriMed Inc. Due to Nail system contains an out of...

The Issue: Nail system contains an out of specification driver-socket which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Universal Ventilator Recalled by Philips Respironics, Inc. Due...

The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2024· Philips Respironics, Inc.

Recalled Item: LifeVentEVO2 Recalled by Philips Respironics, Inc. Due to Potential for...

The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2024· Philips Respironics, Inc.

Recalled Item: Aeris EVO Recalled by Philips Respironics, Inc. Due to Potential for sudden...

The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo O2 Recalled by Philips Respironics, Inc. Due to Potential for...

The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy EV300 Recalled by Philips Respironics, Inc. Due to Potential for...

The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2024· Philips Respironics, Inc.

Recalled Item: Garbin EVO Recalled by Philips Respironics, Inc. Due to Potential for sudden...

The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 19, 2024· Philips Respironics, Inc.

Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Potential for...

The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 18, 2024· GE Medical Systems, SCS

Recalled Item: GE Healthcare Allia IGS 7 OR Recalled by GE Medical Systems, SCS Due to GE...

The Issue: GE HealthCare has become aware of the potential that adhesive material might...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· GE Medical Systems, SCS

Recalled Item: GE Healthcare Interact Discovery RT Recalled by GE Medical Systems, SCS Due...

The Issue: GE HealthCare has become aware of the potential that adhesive material might...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· GE Medical Systems, SCS

Recalled Item: GE Healthcare Allia IGS 5 Pulse Recalled by GE Medical Systems, SCS Due to...

The Issue: GE HealthCare has become aware of the potential that adhesive material might...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· GE Medical Systems, SCS

Recalled Item: GE Healthcare Innova IGS 5 Recalled by GE Medical Systems, SCS Due to GE...

The Issue: GE HealthCare has become aware of the potential that adhesive material might...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· GE Medical Systems, SCS

Recalled Item: GE Healthcare Allia IGS 7 Recalled by GE Medical Systems, SCS Due to GE...

The Issue: GE HealthCare has become aware of the potential that adhesive material might...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· GE Medical Systems, SCS

Recalled Item: GE Healthcare Innova IGS 6 Recalled by GE Medical Systems, SCS Due to GE...

The Issue: GE HealthCare has become aware of the potential that adhesive material might...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· GE Medical Systems, SCS

Recalled Item: GE Healthcare Allia IGS 5 Pulse Recalled by GE Medical Systems, SCS Due to...

The Issue: GE HealthCare has become aware of the potential that adhesive material might...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2024· XENEX Disinfection Services Inc.

Recalled Item: LightStrike Blackout Curtains Recalled by XENEX Disinfection Services Inc....

The Issue: Blackout curtains are no longer recommended as a protective barrier against...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2024· SPINEART SA

Recalled Item: PERLA TL 25D SCREW 45 25-S TLF-DS 45 Recalled by SPINEART SA Due to Due to...

The Issue: Due to receiving information regarding difficulties with the insertion of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter Seprafilm Adhesion Barrier 1 Half Sheet Recalled by Baxter Healthcare...

The Issue: Product was distributed in the United States without proper regulatory approval.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2024· Covidien LP

Recalled Item: Palindrome Precision HSI Chronic Catheter Sport Pack 14.5 Fr/Ch (4.8mm)...

The Issue: Products may not be heparin coated as indicated on the label-leads to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2024· Alcon Research, LLC

Recalled Item: Various Alcon Custom Paks Surgical Procedure Pack containing Oasis 27Ga...

The Issue: Due to complaints of particulates, residue, occlusions, and bent tips for...

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

Class II — Potential Health HazardOngoing