Product Recalls in New Hampshire

Product recalls affecting New Hampshire — including food, drugs, consumer products, medical devices, and vehicles distributed to New Hampshire. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,563 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,563 in last 12 months

Showing 43214340 of 27,899 recalls

Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Zimmer, Inc.

Recalled Item: ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular...

The Issue: Thread form issue for the locking holes in that the locking screws may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Abbott Molecular, Inc.

Recalled Item: Alinity m System Recalled by Abbott Molecular, Inc. Due to The Alinity m...

The Issue: The Alinity m System camera detects whether tubes are "capped." If the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· 3M Company - Health Care Business

Recalled Item: 3M Durapore Surgical Tape Recalled by 3M Company - Health Care Business Due...

The Issue: Select lots of the 3M Durapore Surgical Tape, Catalog Number 1538-118, were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2024· Draeger Medical, Inc.

Recalled Item: Dr¿ger Perseus A500 Anesthesia Workstation Recalled by Draeger Medical, Inc....

The Issue: Unexpected shutdown while operating on battery power.

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

Class I — Serious Health HazardOngoing
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· 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