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 1194111960 of 27,899 recalls

Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: T12. Incorporates wireless electrocardiographic technology to achieve the...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: Q-Tel. The Q-Tel RMS system is a computer-based cardiac and Recalled by...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: Q-Stress/XScribe. Q-Stress or XScribe is a diagnostic device capable of...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: ELI PC. The ELI PC Service automatically converts resting ECG Recalled by...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: S4 and patient cable for the S4 Wireless Telemeter with Recalled by WELCH...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2020· WELCH ALLYN, INC/MORTARA

Recalled Item: H12+ and patient cable for the H12+ Holter Recorders with Recalled by WELCH...

The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew FOOTPRINT Ultra PK Suture Anchor Recalled by Smith & Nephew,...

The Issue: Space between the device and the packaging permits excessive movement which...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Rayner Intraocular Lenses Limited

Recalled Item: RaySert PLUS RSP01. LOT K030. Expiry of 2024-01 - Product Recalled by Rayner...

The Issue: RaySert PLUS RSP01 LOT K030 labeled with an expiry of 2024-01 contained an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Degania Medical Devices Pvt. Ltd.

Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania Medical...

The Issue: Inadequate incoming inspection practices were utilized on thermistor sensors...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2020· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew FOOTPRINT ULTRA PK SUTURE ANCHOR 4.5 Part Number: 72202901...

The Issue: Space between the device and the packaging permits excessive movement which...

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

Class II — Potential Health HazardOngoing