Silex Medical recalls specific laparoscopic instruments due to exposed electrical areas that could cause shock during surgery. Affected models include 5863020 with serial numbers 2222-2253. Consumers should contact the manufacturer for details.
Insulation on the tube did not extend fully to the proximal end of the shaft on the instrument, leaving an exposed (not insulated) area of the shaft closer to the rotator wheel.
Silex Medical is recalling certain laparoscopic instruments because the electrical insulation may not cover the entire shaft, creating an exposed area near the rotator wheel. This could lead to electrical shock during surgical procedures if the instrument is used improperly.
The electrical insulation on the instrument's tube does not fully cover the shaft, leaving an exposed area near the rotator wheel. This exposed section could cause electrical shock if the instrument comes into contact with a conductive surface during surgery.
Surgical teams and medical professionals who use the recalled instruments are most at risk. Patients undergoing surgery with these instruments could face electrical shock.
Check for the model number 5863020 and serial numbers ranging from 2222 to 2253. The product was sold with the UDI-DI code B33158630200 and lot number M28184.
Reach out to Silex Medical for specific instructions on how to verify if your instrument is affected and what to do next.
The recall indicates a potential electrical hazard, so it is not safe to use without verification from the manufacturer.
Contact Silex Medical directly to determine if your instrument is affected and follow their instructions.
Look for the model number 5863020 and serial numbers between 2222 and 2253. Check the UDI-DI code B33158630200 and lot number M28184.
We’ve drafted a message you can send Silex Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1896-2025 — Silex Medical Silex Medical Hello, I own a Silex Medical that is covered by recall Z-1896-2025 from Silex Medical. 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.
