Sklar Instruments recalls two ECONO STERILE medical procedure kits due to packaging issues that may breach sterile barriers. Affected kits have specific model numbers and lot codes. Consumers should check their kits and contact Sklar for details.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Skl:ar Instruments is recalling two types of medical procedure kits because their packaging might break the sterile barrier. This could lead to infections during medical procedures if the kits are used without proper sterility.
The packaging may breach the sterile barrier, which could allow contaminants to enter the kit. This might lead to infections during medical procedures if the kits are used without proper sterility.
Medical professionals and patients using ECONO STERILE medical procedure kits with specific model numbers and lot codes. Those using the kits for procedures where sterility is critical are most at risk.
Check for model numbers 96-2483 (for multiple purposes) or 96-2484 (for foot procedures) with lot codes FSS5 or SK-115. These kits were sold with specific UDI/DI numbers.
Look for model numbers 96-2483 or 96-2484 and lot codes FSS5 or SK-115 on the packaging.
The recall is due to reports of packaging issues that may breach the sterile barrier, potentially leading to infections during medical procedures.
Check the model number and lot code on your kit. If it matches the recalled items, contact Sklar Instruments for further instructions.
The packaging issues may lead to a breach in the sterile barrier, which could cause infections if the kits are used without proper sterility.
We’ve drafted a message you can send Sklar Instruments to request your refund or repair — edit it as you like.
Subject: Recall Z-0926-2025 — Sklar Instruments Sklar Instruments Hello, I own a Sklar Instruments that is covered by recall Z-0926-2025 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.
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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.
