Stryker recalls iBur 4.0mm Coarse Diamond Round surgical burs for potential thermal injury during bone procedures. Affected units have specific lot numbers and were sold for neuro, spine, ENT, and endoscopic surgeries.
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 4.0mm Coarse Diamond Round surgical burs that may overheat at the tip, potentially causing minor tissue damage or requiring medical intervention. This risk occurs during bone cutting procedures for neurosurgery, spine work, ENT, and endoscopic surgeries.
The bur shank can overheat where it meets the distal bushing during use, potentially causing minor tissue damage or requiring medical/surgical intervention. This thermal injury risk occurs when the bur is used for drilling, reaming, or shaping bone tissue.
Surgical professionals using the iBur 4.0mm Coarse Diamond Round burs for bone cutting in neurosurgery, spine procedures, ENT, or endoscopic surgeries. The risk is low and only affects specific lot numbers.
Check for lot numbers: 22248017, 22263017, 22334017, 22348017, 22348027, 23016027, 23095027, 23128017, 23163017, 23179017, 23205017, 23205027, 23205037, 23221017, 23311017, 24004017, 24004027, 24004037. The product is used for bone cutting in neuro, spine, ENT, and endoscopic procedures.
Look for lot numbers on the product packaging: 22248017, 22263017, 22334017, 22348017, 22348027, 23016027, 23095027, 23128017, 23163017, 23179017, 23205017, 23205027, 23205037, 23221017, 23311017, 24004017, 24004027, 24004037.
The recall indicates a potential for minor tissue damage during specific surgical procedures, not general use. The risk is low and only affects the recalled lot numbers.
Check the product lot number to see if it's affected. If it is, contact Stryker for guidance.
Look for lot numbers: 22248017, 22263017, 22334017, 22348017, 22348027, 23016027, 23095027, 23128017, 23163017, 23179017, 23205017, 23205027, 23205037, 23221017, 23311017, 24004017, 24004027, 24004037.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2728-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2728-2024 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.
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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.
