Sklar Instruments recalls ECONO STERILE medical procedure kits with potential sterile packaging breaches. Affected kits have model 96-3500M and lot codes SK-125. Consumers should check packaging details.
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 barriers to breach. This could lead to contamination during medical procedures if the kits are used without proper sterility.
The packaging may breach, allowing non-sterile materials to enter the kit. This could lead to contamination during medical procedures if the kits are used without proper sterility.
Healthcare professionals and medical facilities using the ECONO STERILE kits with model number 96-3500M and lot code SK-125 are most at risk. Patients using these kits during procedures could face contamination risks.
Check for model number 96-3500M and lot code SK-125 on the packaging. The kits are labeled as ECONO STERILE SCALPEL HDL #3 W/METRIC CS/25.
Look for model number 96-3500M and lot code SK-125 on the packaging to confirm if the kit is affected.
The recall states there are reports of packaging issues that may breach the sterile barrier, so affected kits should not be used until the recall is addressed.
The recall does not specify a remedy, so check the packaging details to confirm if the kit is affected. If affected, contact Sklar Instruments for further instructions.
Affected kits have model number 96-3500M and lot code SK-125. Check the packaging label for these details.
We’ve drafted a message you can send Sklar Instruments to request your refund or repair — edit it as you like.
Subject: Recall Z-0937-2025 — Sklar Instruments Sklar Instruments Hello, I own a Sklar Instruments that is covered by recall Z-0937-2025 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.
