Huntleigh Healthcare recalls disposable intraoperative probes with faceplate detachment risk. Affected units include specific model REF DIPP10, lot 7842006001. Stop using immediately to prevent injury.
Faceplate may become detached from the probe body.
Huntleigh Healthcare is recalling disposable intraoperative probes that may have a faceplate that becomes detached from the probe body. This could lead to injury during medical procedures if the detached faceplate causes a sharp injury or blocks the probe's function.
The faceplate may detach from the probe body during use, potentially causing a sharp injury to the user or interfering with the probe's function. This could lead to complications during medical procedures if the detached faceplate obstructs the surgical field or causes injury.
Medical professionals using the recalled probes during surgery are most at risk. Patients receiving these probes could be affected if the faceplate detaches during procedures.
Check for the model REF DIPP10 (box) with lot number 7842006001 or individual probes with lot number 784006001. The product includes a unique identifier (UDI) starting with 05051968036537 for the box and 05051968036544 for individual probes.
Discontinue use of the recalled probes to prevent potential faceplate detachment and injury.
The recalled probes have model REF DIPP10 (box) with lot number 7842006001 or individual probes with lot number 784006001.
Check for the model REF DIPP10 (box) with lot number 7842006001 or individual probes with lot number 784006001. The product includes a unique identifier (UDI) starting with 05051968036537 for the box and 05051968036544 for individual probes.
Stop using the probes immediately to prevent potential faceplate detachment and injury. Contact Huntleigh Healthcare for further instructions.
We’ve drafted a message you can send Huntleigh Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0960-2022 — Huntleigh Healthcare Huntleigh Healthcare Hello, I own a Huntleigh Healthcare that is covered by recall Z-0960-2022 from Huntleigh Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
