Stryker recalls iBur 3.0mm Diamond Round surgical burs for potential thermal injury during bone cutting procedures. Affected units have specific lot numbers and model codes.
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 its iBur 3.0mm Diamond Round surgical burs used for bone cutting. The recall is due to a risk of overheating at the bur shank where it meets the distal bushing, which could cause minor tissue damage or require medical intervention.
The bur shank can overheat at the point where it connects to the distal bushing during use. This overheating may cause minor tissue damage or require medical/surgical intervention to address thermal injury.
Surgical professionals using the iBur 3.0mm Diamond Round burs for bone cutting procedures in neurosurgery, spine surgery, ENT, or endoscopic applications. Patients undergoing these procedures may be at risk if the bur overheats.
Check for lot numbers: 22216017, 22230017, 22334017, 23004017, 23004027, 23009017, 23157017, 23208017, 23233017, 23233027, 24003017. The product code is 8431-012-030D with GTIN 7613327501230.
Identify the lot numbers and product code to confirm if your iBur 3.0mm Diamond Round bur is affected.
The bur shank can overheat at the connection point with the distal bushing, potentially causing minor tissue damage or requiring medical intervention.
Check for lot numbers: 22216017, 22230017, 22334017, 23004017, 23004027, 23009017, 23157017, 23208017, 23233017, 23233027, 24003017. The product code is 8431-012-030D with GTIN 7613327501230.
The recall does not specify a remedy, so contact Stryker directly for guidance.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2725-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2725-2024 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.
