Sklar Instruments recalls ECON:STERILE infant surgical kits with packaging that may breach sterile barriers. Affected kits have model 96-3814 and lot codes starting with 050824. Consumers should check labels for these identifiers.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Sklar Instruments is recalling infant surgical kits that may have packaging issues causing sterile barriers to breach. This could lead to infections during medical procedures if the kits are used without proper sterility.
The packaging may breach the sterile barrier during use, potentially allowing contaminants to enter the surgical site. This could increase infection risk during infant eyelid procedures if the kits are used without proper sterility.
Parents and caregivers using infant surgical kits for eyelid procedures. Those with kits labeled as ECONO STERILE ALFONSO INFANT SPEC STRL CS/10, model 96-3814 are most at risk.
Check for the label: ECONO STERILE ALFONSO INFANT SPEC STRL CS/10. Model number 96-3814 and lot codes starting with 050824 are indicators of affected kits.
Look for the label: ECONO STERILE ALFONSO INFANT SPEC STRL CS/10 with model number 96-3814 and lot codes starting with 050824.
The recall is due to reports of packaging issues that may result in a breach of the sterile barrier, potentially increasing infection risk during infant eyelid procedures.
Check the label for the model number 96-3814 and lot codes starting with 050824. If you have these identifiers, stop using the kit and contact Sklar Instruments for instructions.
The recall record does not mention a remedy or fix. Affected consumers should check the label and contact Sklar Instruments for further instructions.
We’ve drafted a message you can send Sklar Instruments to request your refund or repair — edit it as you like.
Subject: Recall Z-0949-2025 — Sklar Instruments Sklar Instruments Hello, I own a Sklar Instruments that is covered by recall Z-0949-2025 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.
