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Defibtech, LLC: Defibtech DDP-2001: Adult Defibrillation Pads For use with AED

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer

Recall reason: Within the Irish Market, that a Field Safety Notice is being issued due to a select number of authorized labelled Defibtech AED Pads, which have had the authorized label removed and an unauthorized label applied, could potentially lead to expired Defibtech AED Pads appearing as though they are within the acceptable shelf life.there is a possibility of hydrogel drying, which may result in poor electrical connection to the patient, which can reduce the energy delivered to the patient. Recalled by Defibtech, LLC. Distribution: Ireland. Classification (Class II — potential health risk). Affected lots/dates: UDI-DI: 00815098020447, DDP-2001 adult defibrillation pads, single pac

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Category Product Recalls & Refunds
Location CT
Eligibility U.S. consumers who own or purchased the recalled medical device. Contact the manufacturer or the retailer/pharmacy where you purchased it to arrange for a free correction, repair, or replacement. Have the model number ready if possible.
Source Official Source ↗
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