Sklar Instruments recalls ECONO STERILE medical procedure kits with model numbers 96-2243 to 96-2959 due to packaging issues that could breach sterile barriers. Affected kits include specific lot codes and model variants.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Sklar Instruments is recalling specific ECONO STERILE medical procedure kits because packaging issues might cause the sterile barrier to break. This could lead to contamination during medical procedures if the kits are used without proper sterility.
The packaging may not seal properly, leading to a breach in the sterile barrier. This could allow contaminants to enter the kit, potentially causing infections or other complications during medical procedures.
Healthcare professionals using these kits for medical procedures are most at risk. Patients could be exposed to contamination if the sterile barrier is compromised during surgery or other medical treatments.
Check for model numbers 96-2243 to 96-2959 on the kits. Look for specific lot codes: SK-112, SK-115, SK-116, SK-117, SK-118, or SK-129. These kits are labeled as ECONO STERILE ARMY RETR or SENN RETR.
Identify the model number (96-2243 to 96-2959) and lot code (SK-112 to SK-129) on the kit packaging.
The recall does not require immediate stop use. However, if you have the affected kits, you should check the model and lot codes before using.
The recall does not specify a remedy, so you should check the model and lot codes to confirm if your kit is affected. If it is, contact Sklar Instruments for further instructions.
Yes, a breach could lead to contamination during medical procedures, potentially causing infections or other complications.
We’ve drafted a message you can send Sklar Instruments to request your refund or repair — edit it as you like.
Subject: Recall Z-0933-2025 — Sklar Instruments Sklar Instruments Hello, I own a Sklar Instruments that is covered by recall Z-0933-2025 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.
