Sklar Instruments recalls 31 specific ECONO STERILE medical procedure kits due to packaging issues that could breach the sterile barrier. Affected kits have listed model numbers and lot codes.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Sklar Instruments is recalling 31 different ECONO STERILE medical procedure kits because packaging issues might cause the sterile barrier to be breached. This could lead to infections during medical procedures if the kits are used without proper sterility.
The packaging may have defects that allow contamination, potentially breaching the sterile barrier. This could lead to infections during medical procedures if the kits are used without proper sterility.
Healthcare professionals and medical facilities that use these specific ECONO STERILE kits for orthopedic surgery are most at risk. Patients could face infection if the kits are used without a properly intact sterile barrier.
Check for model numbers listed in the recall: 96-2352A through 96-2745A. Also look for specific lot codes like HSI, SK-130, or FSF12 among the packaging details.
Identify the model number on the kit's packaging to see if it matches the recalled list (96-2352A through 96-2745A).
Reach out to Sklar Instruments directly for confirmation of the kit's model and lot code to determine if it's affected.
The recall states packaging issues may breach the sterile barrier, but no specific injuries or infections have been reported. The risk is low but requires careful handling.
Check the model number on the packaging (96-2352A through 96-2745A) and the lot code (e.g., HSI, SK-130, FSF12).
The recall does not mention any remedy or fix; affected kits should be checked and potentially discarded if not confirmed safe.
We’ve drafted a message you can send Sklar Instruments to request your refund or repair — edit it as you like.
Subject: Recall Z-0954-2025 — Sklar Instruments Sklar Instruments Hello, I own a Sklar Instruments that is covered by recall Z-0954-2025 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.
