Synthes recalls sciatic nerve retractors with part number 03.100.014 due to potential microspores forming in the handle that could allow fluid entry. Affected units include specific lot numbers.
There is a potential for microspores to form on the hollow handle of the Sciatic Nerve Retractor. The pores may increase in size, allowing fluid to enter the hollow handle.
Synthes is recalling sciatic nerve retractors with part number 03.100.014 because microspores may form in the hollow handle. This could allow fluid to enter the handle, potentially causing complications during medical procedures.
Microspores may form inside the hollow handle of the retractor, and if they grow larger, fluid could enter the handle. This could lead to complications during medical procedures if the device is used without proper checks.
Medical professionals using the recalled sciatic nerve retractors are most at risk. Patients undergoing procedures with these devices could be affected if the retractors are used without proper precautions.
Check for the part number 03.100.014 on the retractor. Affected units have specific lot numbers listed in the recall notice, including T104993 through T152809.
Identify the part number and lot numbers to confirm if your retractor is affected.
The recall indicates a potential risk, but the product is not unsafe if used with proper checks. Affected units should be checked against the listed lot numbers.
The recall does not specify a remedy, so check the product details against the listed lot numbers to determine if it is affected.
Look for the part number 03.100.014 and check if your lot number matches the list provided in the recall notice.
We’ve drafted a message you can send Synthes to request your refund or repair — edit it as you like.
Subject: Recall Z-1759-2018 — Synthes Synthes Hello, I own a Synthes that is covered by recall Z-1759-2018 from Synthes. 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.
