Sklar Instruments recalls ECONO STERILE medical procedure kits with potential sterile barrier breaches. Affected kits may not maintain sterility during use.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Skl:ar Instruments is recalling ECONO STERILE medical procedure kits that may have packaging issues causing sterile barrier breaches. This could lead to infections if used improperly.
The packaging may breach the sterile barrier during use, potentially exposing medical instruments to contaminants. This could lead to infections if the kits are used without proper sterility.
Medical professionals and patients using the ECONO STERILE TROUSSEAU DILATOR CS/25 kits with model number 941-0191 are affected. Those performing tracheal procedures are at higher risk.
Check for the model number 941-0191 on the packaging. The kits are labeled as ECONO STERILE TROUSSEAU DILATOR CS/25 for tracheal procedures. Lot codes include 9249410191.
Verify the model number 941-0191 and lot code 9249410191 on the packaging.
The model number is 941-0191.
Reports of packaging issues that may result in a breach of the sterile barrier.
Check for the model number 941-0191 and lot code 9249410191 on the packaging.
We’ve drafted a message you can send Sklar Instruments to request your refund or repair — edit it as you like.
Subject: Recall Z-0927-2025 — Sklar Instruments Sklar Instruments Hello, I own a Sklar Instruments that is covered by recall Z-0927-2025 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.
