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. 2,536 recalls have been distributed to New Hampshire in the last 12 months.
Showing 9321–9340 of 27,899 recalls
Recalled Item: NEO DELTA Self Safe T Recalled by Delta Med SpA Due to Problems related to...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELTAVEN Y DNL Safety I.V. Catheter in Pur with closed Recalled by Delta Med...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO DELTA SELFSAFE PUR T Recalled by Delta Med SpA Due to Problems related...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WOLF-PAK Self Safe Safety IV Catheter: a) b) Recalled by Delta Med SpA Due...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELTAVEN Safety I.V. Catheter in Pur with closed system: a) Recalled by...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELTAVEN FASTFLASH Recalled by Delta Med SpA Due to Problems related to the...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEO DELTA SELFSAFE PUR 1 Recalled by Delta Med SpA Due to Problems related...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DELTAVEN Y Recalled by Delta Med SpA Due to Problems related to the...
The Issue: Problems related to the sterilization of the medical devices; possible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien HysteroLux Fluid Management System Control Unit Recalled by WOM...
The Issue: When the display of inflow volume to the uterus reaches 32450 ml, the fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermoScientific Oxoid Antimicrobial Susceptibility Discs Rx only Made in...
The Issue: Out of Specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Plus Ventilator with Software Versions 3.00 and...
The Issue: It has been identified that ventilators equipped with High Flow Therapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator with Software Versions 3.00 and 3.10....
The Issue: It has been identified that ventilators equipped with High Flow Therapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemotherm CE Dual Reservoir Cooler/Heater Recalled by Gentherm Medical, LLC...
The Issue: There is a potential risk of device contamination and patient infection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argyle UVC Insertion Tray containing Safety Scalpel N11 (vendor part...
The Issue: The current Argyle UVC Insertion Tray does not include a specific IFU to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235- designed to produce and deliver a proton beam Recalled by Ion...
The Issue: Users may be misled by the popup message displayed by the Proton Therapy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Suture Anchor Recalled by Arthrex, Inc. Due to Not properly sterilized,...
The Issue: Not properly sterilized, because the outer pouch seal on the Tyvek header...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy 100 Recalled by Philips Respironics, Inc. Due to The polyester-based...
The Issue: The polyester-based polyurethane (PE-PUR) foam may degrade into particles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A-Series BiPAP A 40 Recalled by Philips Respironics, Inc. Due to The...
The Issue: The polyester-based polyurethane (PE-PUR) foam may degrade into particles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A-Series BiPAP Hybrid A30 (not marketed in US) Recalled by Philips...
The Issue: The polyester-based polyurethane (PE-PUR) foam may degrade into particles...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoreValve Evolut PRO Delivery Catheter System Recalled by Medtronic Heart...
The Issue: Due to reports of actuator separation for various delivery catheter systems....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.