Stryker recalls certain iBur 3.0mm Coarse Diamond Round surgical burs for potential thermal injury during bone procedures. Affected units may cause minor tissue damage requiring medical attention.
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 specific surgical burs that could overheat during bone cutting procedures, potentially causing minor tissue damage or requiring medical intervention. This recall affects surgeons and medical professionals using the product for spinal, neuro, 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 during bone cutting procedures like drilling, reaming, and shaping.
Surgeons and medical professionals using the Stryker iBur 3.0mm Coarse Diamond Round burs for bone cutting in spinal, neuro, ENT, or endoscopic procedures. Those most at risk are practitioners using the affected lot numbers.
Check for the product model 'Stryker iBur 3.0mm Coarse Diamond Round, Distal Bend' with lot numbers 22230017, 22333017, 22342017, 23011017, 23093017, 23172017, 23188017, 23221017, 23311017, or 24004027.
Verify the lot number on the product label to confirm if it's affected.
The bur shank can overheat where it meets the distal bushing during use, potentially causing minor tissue damage or requiring medical/surgical intervention.
These burs are used for bone cutting in neuro, spine, ENT, and endoscopic procedures.
Check for lot numbers 22230017, 22333017, 22342017, 23011017, 23093017, 23172017, 23188017, 23221017, 23311017, or 24004027.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2727-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2727-2024 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.
