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. 2,508 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,508 in last 12 months

Showing 1292112940 of 27,899 recalls

Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: External Toco Transducer (M1355A) Recalled by Pacific Medical Group Inc. Due...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Button-Style Tocotransducer (Nautilus) Recalled by Pacific Medical Group...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Loop-Style Ultrasound Transducer (Nautilus) Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS chemistry Products K+ Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Users may experience intermittent slide dispense issues with some cartridges...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Exactech, Inc.

Recalled Item: Ergo 3.2mm K-wire - Product Usage: The devices is used Recalled by Exactech,...

The Issue: Potential for the wire to fracture at the threads and remain in the glenoid.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Novarad Corporation

Recalled Item: NovaPACS Diagnostic Viewer. NovaPACS is a picture archiving and...

The Issue: The firm received a report of an atypical dataset being generated. When...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Users may experience intermittent slide dispense issues with some cartridges...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· MEDTECH SAS

Recalled Item: Rosa Brain 3.0 Recalled by MEDTECH SAS Due to The instrument holder may be...

The Issue: The instrument holder may be sent on a trajectory that is not within the...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 10, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Users may experience intermittent slide dispense issues with some cartridges...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2019· Medline Industries Inc

Recalled Item: MEDLINE ELECTRIC SURGICAL CLIPPER AND BASE Recalled by Medline Industries...

The Issue: The recall is being conducted due to a potential defective component on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2019· CooperSurgical, Inc.

Recalled Item: Embryology Heated Plate within the RI Witness Recalled by CooperSurgical,...

The Issue: The touchpad may not work properly after cleaning.

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

Class III — Low RiskOngoing
Medical DeviceSeptember 4, 2019· Elekta Inc

Recalled Item: Monaco RTP System Recalled by Elekta Inc Due to It is possible that the...

The Issue: It is possible that the forced electron density settings will be changed for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2019· Elekta Inc

Recalled Item: Monaco RTP System Recalled by Elekta Inc Due to It is possible that the...

The Issue: It is possible that the forced electron density settings will be changed for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2019· GE Healthcare, LLC

Recalled Item: Achilles Insight Bone Sonometer Recalled by GE Healthcare, LLC Due to...

The Issue: Certain Achilles Express and Achilles Insight systems were shipped with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2019· GE Healthcare, LLC

Recalled Item: Achilles Express Bone Sonometer Recalled by GE Healthcare, LLC Due to...

The Issue: Certain Achilles Express and Achilles Insight systems were shipped with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· Philips Ultrasound Inc

Recalled Item: Transducer S8-3t UDI (01)00884838067523 Can be used with: Recalled by...

The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· Philips Ultrasound Inc

Recalled Item: Transducer S7-3t UDI (01)00884838061439 Can be used with: Recalled by...

The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· Spacelabs Healthcare, Inc.

Recalled Item: Xhibit Central Recalled by Spacelabs Healthcare, Inc. Due to The firm...

The Issue: The firm received reports of loss of audio alarm after a power failure or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· GE Healthcare, LLC

Recalled Item: ApexPro Telemetry Server System. Also identified as Modification To: ApexPro...

The Issue: May not provide visual and/or audible alarms at the CARESCAPE Central...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2019· Philips Ultrasound Inc

Recalled Item: Transducer S7-3t UDI (01)00884838067530 Used as accessory with: Recalled by...

The Issue: The firm has discovered an issue associated with some Transesophageal (TEE)...

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

Class II — Potential Health HazardOngoing