Sklar Instruments recalls specific sterile medical nail clipper kits due to packaging defects that may breach sterile barriers. Affected models include ECONO STERILE D/A NAIL NIPPER 5.75" STER CS5 and others with model numbers 96-2424A through 96-2671A.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Sklar Instruments is recalling six specific sterile medical nail clipper kits because packaging issues could breach the sterile barrier. This risk could lead to infections if the kits are used improperly during medical procedures.
The packaging defects could compromise the sterile barrier, potentially allowing contamination. This might lead to infections if the kits are used without a properly maintained sterile environment.
Healthcare professionals using these sterile kits for nail procedures are most at risk. Patients receiving these kits during medical treatments may also be affected.
Check for model numbers 96-2424A through 96-2671A on the packaging. Look for lot codes SK-112, SK-131, or SK-118 on the labels.
Look for model numbers 96-2424A through 96-2671A and lot codes SK-112, SK-131, or SK-118 on the packaging.
Sklar Instruments reports packaging issues that may breach the sterile barrier, potentially leading to contamination during medical procedures.
The affected models include ECONO STERILE D/A NAIL NIPPER 5.75" STER CS5 (model 96-2424A), ECONO STERILE TISS NIPPER 14MM CVX 5"CS/25 (model 96-2427), and others with model numbers 96-2666 through 96-2671A.
The recall does not require immediate stop use; however, affected users should check their product labels and 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-0932-2025 — Sklar Instruments Sklar Instruments Hello, I own a Sklar Instruments that is covered by recall Z-0932-2025 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.
