Sklar Instruments recalls 50+ ECONO STERILE medical procedure kits with packaging issues that may breach sterile barriers. Affected kits include specific models and lot codes. Consumers should check their product labels for model numbers and lot codes to determine if affected.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Sklar Instruments is recalling 50 different ECONO STERILE medical procedure kits due to packaging issues that may breach the sterile barrier. This could lead to contamination during medical procedures if the kits are used without proper sterility.
The packaging may have issues that cause the sterile barrier to be breached, potentially leading to contamination of medical instruments during procedures. This could increase the risk of infection for patients.
Healthcare professionals and medical facilities that use these kits are most at risk. Patients using these kits during procedures could be exposed to contamination if the sterile barrier is compromised.
Check the product label for model numbers (e.g., 94-0286, 94-0290) and lot codes (e.g., FSF21, SK-115) listed in the recall notice. The kits are labeled as ECONO STERILE medical procedure kits.
Look for model numbers and lot codes on the product label to determine if your kit is affected.
The recall states that these kits may have packaging issues that could breach the sterile barrier, so they should not be used until the recall is completed.
Check the model number and lot code on your kit's label against the list provided in the recall notice.
The recall does not specify a remedy, so you should contact Sklar Instruments directly for guidance.
We’ve drafted a message you can send Sklar Instruments to request your refund or repair — edit it as you like.
Subject: Recall Z-0939-2025 — Sklar Instruments Sklar Instruments Hello, I own a Sklar Instruments that is covered by recall Z-0939-2025 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.
