Mani recalls two trocar kit models (MTK23S and MTK25S) due to potential packaging defects that could compromise sterile barriers. Affected kits were sold with specific lot numbers and expiration dates.
A packaging defect may compromise the sterile barrier.
Mani is recalling two types of trocar kits (MTK23S and MTK25S) because a packaging defect might compromise the sterile barrier. This could lead to contamination if the kits are used without proper sterility.
The packaging defect could compromise the sterile barrier, potentially allowing contamination of the kits. This might lead to infection if the kits are used without proper sterility.
Medical professionals who use these trocar kits for procedures are likely affected. The risk is low as the defect is packaging-related and not a direct hazard to users.
Check for the model numbers MTK23S or MTK25S on the packaging. The kits were sold with specific lot numbers and expiration dates listed in the recall notice.
Inspect the packaging for the model number (MTK23S or MTK25S) and lot number.
The recall states there is a packaging defect that may compromise the sterile barrier, but does not specify the exact defect.
Three kits are contained in one box, with one sterile kit consisting of three pieces.
Lot numbers and expiration dates are listed in the recall: MTK23S (Lot V210028903, exp. 2024-03), MTK25S (Lots V210009900, V210006701, V210009101, V220016001 with various expiration dates).
We’ve drafted a message you can send Mani to request your refund or repair — edit it as you like.
Subject: Recall Z-1468-2023 — Mani Mani Hello, I own a Mani that is covered by recall Z-1468-2023 from Mani. 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.
