Sklar Instruments recalls three ECONO STERILE medical procedure kits with packaging issues that may breach sterile barriers. Affected kits include specific models and lot codes. Consumers should contact Sklar for details.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Sklar Instruments is recalling three medical procedure kits due to packaging problems that could compromise sterile barriers. This risk could lead to infections during medical procedures if the kits are used without a properly sealed barrier.
The packaging may not seal properly, potentially breaching the sterile barrier. This could allow contamination during medical procedures, increasing infection risk if the kits are used without a properly sealed barrier.
Healthcare providers and medical facilities using the recalled ECONO STERILE kits for procedures like cervical biopsies. Those using the specific model numbers and lot codes listed are most at risk.
Check for the model numbers 96-4113, 96-4144A, or 96-4145A on the kit packaging. Look for lot codes SK-133, HSC21, or HSC21 for the specific kits.
Look for model numbers 96-4113, 96-4144A, or 96-4145A and lot codes SK-133, HSC21, or HSC21.
The recall states that packaging issues may breach the sterile barrier, so they are not safe to use without verification.
Check for model numbers 96-4113, 96-4144A, or 96-4145A and lot codes SK-133, HSC21, or HSC21.
Contact Sklar Instruments for details on how to handle the kits, as the recall remedy is not specified.
We’ve drafted a message you can send Sklar Instruments to request your refund or repair — edit it as you like.
Subject: Recall Z-0943-2025 — Sklar Instruments Sklar Instruments Hello, I own a Sklar Instruments that is covered by recall Z-0943-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
