Product Recalls in Vermont
Product recalls affecting Vermont — including food, drugs, consumer products, medical devices, and vehicles distributed to Vermont. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,515 recalls have been distributed to Vermont in the last 12 months.
Showing 5981–6000 of 47,027 recalls
Recalled Item: libigrow RED DRAGON+ Recalled by Pyramids Wholesale Inc. Due to Undeclared...
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GoHARD 25000 Recalled by Pyramids Wholesale Inc. Due to Undeclared Sildenafil
The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.