Sklar Instruments recalls ECON:STERILE medical procedure kits with packaging issues that may breach sterile barriers. Affected kits have model 96-2224A and lot codes HSI. No remedy stated in recall.
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 eye surgery if the kits are used without proper sterility.
The packaging may breach the sterile barrier during handling or storage, potentially exposing the kits to contaminants. This could lead to infections if the kits are used without proper sterility.
Medical professionals using these kits for eye surgery are most at risk. Patients undergoing eye procedures with these kits could face infection risks.
Check for model number 96-2224A on the kit. Lot codes starting with HSI indicate affected units. These kits are labeled for eye surgery procedures.
Look for model number 96-2224A and lot codes starting with HSI on the kit.
The recall is due to reports of packaging issues that may breach the sterile barrier, potentially leading to infections during eye surgery.
The recall record does not specify a remedy, so check the kit for model number 96-2224A and lot codes starting with HSI to confirm if it's affected.
The hazard is described as packaging issues that may breach the sterile barrier, which could lead to infections but not direct serious injuries like cuts or fires.
We’ve drafted a message you can send Sklar Instruments to request your refund or repair — edit it as you like.
Subject: Recall Z-0951-2025 — Sklar Instruments Sklar Instruments Hello, I own a Sklar Instruments that is covered by recall Z-0951-2025 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.
