Stryker recalls iBur 5.0mm Coarse Diamond Round burs for potential thermal injury during bone cutting procedures. Affected units have specific lot numbers and were sold for neuro, spine, ENT, and endoscopic applications.
Potential for the product to exhibit temperatures higher than specification where the bur shank meets the distal bushing. Temperatures higher than specification may lead to the potential for minor tissue/structure damage or tissue/structure damage from thermal injury which may need medical/surgical intervention.
Stryker is recalling certain iBur 5.0mm Coarse Diamond Round burs used in bone cutting procedures. The burs may overheat at the shank-bushing interface, risking minor tissue damage or requiring medical intervention.
The bur shank can overheat where it meets the distal bushing during bone cutting. This overheating may cause minor tissue damage or require medical/surgical intervention.
Medical professionals using the iBur burs for bone cutting in neuro, spine, ENT, or endoscopic procedures. Those with specific lot numbers are most at risk.
Check for lot numbers: 22224017, 22227017, 23087017, 23157017, 23188017, 23342017. The product is used for neuro, spine, ENT, and endoscopic procedures.
Look for lot numbers on the product: 22224017, 22227017, 23087017, 23157017, 23188017, 23342017.
The iBur is used for neuro, spine, ENT, and endoscopic procedures involving bone cutting.
Overheating may cause minor tissue damage or require medical/surgical intervention.
Check the lot number: 22224017, 22227017, 23087017, 23157017, 23188017, or 23342017.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2729-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2729-2024 from Stryker. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
