Sheathing Technologies recalls 50-pack of vaginal/rectal ultrasound probe covers with viral barrier that may cause contamination during use. Affected units have specific dimensions and lot numbers.
Vaginal/rectal ultrasound probe covers with a viral barrier may have product defects, which may result in contamination during use, posing an infection risk.
Sheathing Technologies is recalling 50-pack of vaginal/rectal ultrasound probe covers that may have defects causing contamination and infection risk. This recall affects medical devices used during ultrasound procedures.
The viral barrier on these ultrasound probe covers may have defects that lead to contamination during medical procedures. This could increase the risk of infection for patients and healthcare workers.
Healthcare providers and patients using vaginal/rectal ultrasound probes with these covers. Those with specific product dimensions and lot numbers are most at risk.
Check for the product name 'Sheathes3D Seamless Viral Barrier', 7/8"D Tapered to 2.9"W x 11.8"L, and lot number 25-45. The expiration date is November 1, 2028.
Look for the product name, dimensions, and lot number on the packaging to confirm if it's affected.
The viral barrier on these ultrasound probe covers may have defects that could lead to contamination during use, posing an infection risk.
The recall record does not specify a remedy, so check the product details to see if it's affected and contact Sheathing Technologies for further instructions.
Check for the product name 'Sheathes3D Seamless Viral Barrier', 7/8"D Tapered to 2.9"W x 11.8"L, and lot number 25-45.
We’ve drafted a message you can send Sheathing Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-1006-2026 — Sheathing Technologies Sheathing Technologies Hello, I own a Sheathing Technologies that is covered by recall Z-1006-2026 from Sheathing Technologies. 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.
