Sklar Instruments recalls 54 medical procedure kits with specific model numbers and lot codes due to packaging issues that may breach sterile barriers. Consumers should check their kits for model numbers and lot codes listed in the recall notice.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Sklar Instruments is recalling 54 different medical procedure kits that may have packaging issues causing sterile barriers to breach. This could lead to contamination during medical procedures if the kits are used without proper sterility.
The packaging may not seal properly, potentially allowing contamination to reach the sterile contents. This could lead to infection risks during medical procedures if the kits are used without proper sterility.
Healthcare professionals and medical facilities that use these specific ECONO STERILE procedure kits are most at risk. The recall affects kits sold with model numbers and lot codes listed in the notice.
Check the model number on the kit (e.g., 941-0918) and lot codes (e.g., MSS8) listed in the recall notice. The kits are labeled as ECONO STERILE medical procedure kits.
Look for the model number (e.g., 941-0918) and lot codes (e.g., MSS8) on the kit to confirm if it is affected.
The recall is due to reports of packaging issues that may result in a breach of the sterile barrier.
Check the model number and lot codes on your kit against the list provided in the recall notice.
The recall notice does not specify a remedy, so affected kits should be checked for proper sterility before use.
We’ve drafted a message you can send Sklar Instruments to request your refund or repair — edit it as you like.
Subject: Recall Z-0941-2025 — Sklar Instruments Sklar Instruments Hello, I own a Sklar Instruments that is covered by recall Z-0941-2025 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.
