Stryker recalls iBur 3.0mm Precision Round surgical burs for potential thermal injury during bone cutting. Affected units have specific lot numbers and were sold for spine, neuro, ENT procedures. Contact Stryker for details.
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 3.0mm Precision Round surgical burs that may overheat at the tip, risking minor tissue damage or requiring medical intervention. This recall affects specific lot numbers used in spine, neuro, and ENT surgeries.
The bur shank can overheat at 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 bone cutting in specific medical procedures.
Surgical professionals using the iBur 3.0mm Precision Round burs for bone cutting in spine, neuro, and ENT procedures. Patients undergoing surgery with these burs may face minor tissue damage risks.
Check for lot numbers: 22224017, 22234017, 22234027, 22250017, 22293017, 22299017, 23157017, 23179017, 23179027, 23299017. The product is sold for spine, neuro, and ENT surgeries under the Stryker brand.
Identify the lot number on the product packaging to confirm if it's affected (22224017, 22234017, 22234027, 22250017, 22293017, 22299017, 23157017, 23179017, 23179027, 23299017).
Reach out to Stryker Corporation directly for further instructions on the recall.
The burs may overheat at the tip during use, potentially causing minor tissue damage or requiring medical/surgical intervention.
These burs are used for bone cutting in spine, neuro, and ENT surgeries.
Check the lot number on the product packaging; affected units have specific lot numbers listed in the recall.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-2722-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-2722-2024 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.
