Sklar Instruments recalls specific sterile medical procedure kits for nasal use due to packaging defects that may breach sterile barriers. Affected kits have model numbers 96-2236, 96-2237M, or 96-2238 with listed lot codes.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Sklar Instruments is recalling certain sterile medical procedure kits for nasal procedures because packaging issues could breach the sterile barrier. This risk could lead to infections if the kits are used without a properly sealed barrier.
The packaging may not seal properly, allowing contaminants to enter the sterile kit. This could lead to infections if the kit is used without a fully intact sterile barrier.
Healthcare providers and patients using the recalled sterile kits for nasal procedures. Those handling the kits without proper checks are most at risk.
Check for model numbers 96-2236, 96-2237M, or 96-2238 on the kit. Lot codes SK-129, SK-130, SK-131, or SK-133 may also indicate affected units.
Look for model numbers 96-2236, 96-2237M, or 96-2238 with specific lot codes listed in the recall.
The recall states packaging issues may breach the sterile barrier, so they are not safe to use without checking the recall list.
Model numbers 96-2236, 96-2237M, and 96-2238 with specific lot codes are affected.
Check the model number and lot code on the kit; affected kits have model numbers 96-2236, 96-2237M, or 96-2238 with lot codes SK-129, SK-130, SK-131, or SK-133.
We’ve drafted a message you can send Sklar Instruments to request your refund or repair — edit it as you like.
Subject: Recall Z-0930-2025 — Sklar Instruments Sklar Instruments Hello, I own a Sklar Instruments that is covered by recall Z-0930-2025 from Sklar Instruments. 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.
