Zimmer Biomet recalls specific lots of Gentle Threads Interference Screw (Model 905617) due to potential infection from overexposure during EtO sterilization. Affected lots include 207910.
Specific lots of the device were overexposed during EtO sterilization. This may lead to revision due to infection from loss of sterile barrier during over-exposure cycle.
Zimmer Biomet is recalling specific lots of Gentle Threads Interference Screws (Model : 905617) because they may have been overexposed during sterilization, increasing infection risk during soft tissue procedures. This recall affects surgeons and medical facilities using the specific lot numbers.
The device may have been overexposed during ethylene oxide (EtO) sterilization, which can compromise the sterile barrier. This could lead to infection during soft tissue reattachment procedures if the device is used without proper sterilization.
Surgeons and medical facilities using the specific lot number 207910 of the Gentle Threads Interference Screw (Model 905617) for ankle/foot or knee procedures are affected. Patients undergoing these procedures with the recalled lot are at risk of infection.
Check the lot number on the device packaging. The affected lot is 207910. The product is used for soft tissue reattachment procedures in the ankle/foot and knee.
Look for the lot number on the device packaging. The affected lot is 207910.
The product may have been overexposed during sterilization, increasing infection risk. Affected lots should not be used.
Check the lot number on the device packaging. If it is 207910, stop using it and contact Zimmer Biomet for instructions.
The recall record does not specify a replacement process or remedy.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-1734-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-1734-2018 from Zimmer Biomet. 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.
