Sklar Instruments recalls ECONO STERILE medical procedure kits with packaging issues that may breach sterile barriers. Affected kits have model 96-4921A and lot code FSF20. Consumers should check packaging labels for recall details.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Sklar Instruments is recalling ECONO STERILE medical procedure kits that may have packaging issues causing sterile barrier breaches. This could lead to infections during medical procedures if the kits are used without proper sterility.
The packaging may not seal properly, potentially allowing contamination. This could compromise the sterile environment needed for medical procedures, increasing infection risk.
Medical professionals and patients using the ECONO STERILE kits with model number 96-4921A and lot code FSF20 are affected. Those performing procedures requiring sterile environments are at higher risk.
Check for the model number 96-4921A and lot code FSF20 on the packaging. The kits are labeled as ECONO STERILE BLAKE GALLSTONE FCP CVD 8"CS25.
Look for model number 96-4921A and lot code FSF20 on the packaging to confirm if the kit is affected.
The recall is due to reports of packaging issues that may result in a breach of the sterile barrier.
Check for the model number 96-4921A and lot code FSF20 on the packaging. The kits are labeled as ECONO STERILE BLAKE GALLSTONE FCP CVD 8"CS25.
The recall record does not specify a remedy, so contact Sklar Instruments directly for guidance.
We’ve drafted a message you can send Sklar Instruments to request your refund or repair — edit it as you like.
Subject: Recall Z-0940-2025 — Sklar Instruments Sklar Instruments Hello, I own a Sklar Instruments that is covered by recall Z-0940-2025 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.
