Sklar Instruments recalls 9 specific ECONO STERILE medical procedure kits due to packaging issues that could breach the sterile barrier. Affected kits have model numbers 96-2603 to 96-3002 with lot code SK-119. Consumers should check their kit labels for these models and lot codes.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Sklar Instruments is recalling nine specific ECONO STERILE medical procedure kits because their packaging might not stay sterile, which could lead to infections during medical procedures. This is a serious issue for people using these kits for gynecological or surgical procedures.
The packaging in these kits may have issues that cause the sterile barrier to be breached. This could lead to contamination of the medical instruments, increasing the risk of infection during procedures.
Healthcare providers and patients using the recalled ECONO STERILE medical procedure kits for gynecological or surgical procedures are most at risk. These kits were sold with specific model numbers and lot codes.
Check the label for model numbers 96-2603 to 96-3002 and lot code SK-119. The kits are labeled as ECONO STERILE GRAVES SPEC STRL or PEDERSON SPEC STRL with specific sizes (SM, MD, LG) and packaging types (BX/25, BX/50, CS/50).
Look for model numbers 96-2603 to 96-3002 and lot code SK-119 on the packaging.
The recall is due to reports of packaging issues that may breach the sterile barrier, potentially leading to contamination during medical procedures.
The affected kits have model numbers 96-2603 to 96-3002 with lot code SK-119, including specific sizes like SM, MD, and LG for gynecological and surgical use.
Check your kit label for the model numbers and lot code. If it matches the affected models and lot code, 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-0944-2025 — Sklar Instruments Sklar Instruments Hello, I own a Sklar Instruments that is covered by recall Z-0944-2025 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.
