Ninepoint Medical recalls NvisionVLE Low-Profile Optical Probes with catalog numbers 95501-LP and 95501-LP-5 due to risk of distal tips detaching during use. Affected units include specific lot numbers.
Distal tips of the probes may detach from the probe shaft during use.
Ninepoint Medical is recalling NvisionVLE Low-Profile Optical Probes with catalog numbers 95501-LP and 95501-LP-5 because the distal tips may detach during use. This could lead to injury if the probe is not securely attached to the imaging system.
The distal tips of the probes may detach from the probe shaft while in use. This could cause the probe to become unstable or move unexpectedly, potentially leading to injury if the probe is not securely attached to the imaging system.
Users of the NvisionVLE Low-Profile Optical Probe for medical imaging are affected. Patients and medical staff using the probe with the NvisionVLE Imaging System are at risk if the distal tips detach.
Check for catalog numbers 95501-LP or 95501-LP-5 on the product. Affected units include lot numbers 005196, 005251, and 005275.
Look for catalog numbers 95501-LP or 95501-LP-5 and lot numbers 005196, 005251, or 005275 on the product.
The distal tips of the probes may detach from the probe shaft during use, which could lead to injury if the probe is not securely attached to the imaging system.
Catalog numbers 95501-LP and 95501-LP-5 are affected.
Lot numbers 005196, 005251, and 005275 are affected.
We’ve drafted a message you can send Ninepoint Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1781-2018 — Ninepoint Medical Ninepoint Medical Hello, I own a Ninepoint Medical that is covered by recall Z-1781-2018 from Ninepoint Medical. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
