Sklar Instruments recalls ECONO STERILE medical procedure kits with potential sterile packaging breaches. Affected kits have model 96-4780A and lot codes HSI. Consumers should check packaging labels for recall 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 infections if used improperly. Affected kits have model number 96-4:780A and lot codes HSI.
The packaging may breach, allowing contaminants to enter the sterile medical kits. This could lead to infections if the kits are used without proper sterility. The risk is not immediate but depends on the integrity of the packaging.
Orthopedic surgery patients and medical professionals using the ECONO STERILE kits with model 96-4780A and lot codes HSI. Those at highest risk are users who rely on the sterile packaging for infection prevention.
Check for the model number 96-4780A and lot codes HSI on the packaging. The kits are labeled as ECONO STERILE LEMPERT BONE RONG 6.25" STER25 for orthopedic surgery use.
Look for model number 96-4780A and lot codes HSI on the packaging.
The recall is due to reports of packaging issues that may breach the sterile barrier, potentially leading to infections.
Check the packaging for model number 96-4780A and lot codes HSI. If you have these, contact Sklar Instruments for further instructions.
The recall addresses potential packaging breaches that could lead to infections, not immediate serious injuries.
We’ve drafted a message you can send Sklar Instruments to request your refund or repair — edit it as you like.
Subject: Recall Z-0952-2025 — Sklar Instruments Sklar Instruments Hello, I own a Sklar Instruments that is covered by recall Z-0952-2025 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.
