Stryker recalls C2 Nerve Monitor models due to possible use errors causing nerve injury during surgery. Affected units include specific serial numbers and models.
Stryker C2 NerveMonitor's design and instructions may not optimally address usability issues related to the functionality of the device, which may result in use errors potentially causing or contributing to nerve injury.
Stryker is recalling its C2 Nerve Monitor system because its design and instructions might lead to use errors that could cause nerve injury during surgery. This affects specific models and serial numbers sold for surgical use.
The device's design and instructions may not handle usability issues well, which could lead to mistakes during surgery. These errors might cause nerve injury if the monitor is used incorrectly.
Surgical teams using the C2 Nerve Monitor during operations are most at risk. The recall applies to specific models and serial numbers sold for intra-operative nerve monitoring.
Check for the model number 5140-508-240 and serial number starting with 07613327177329. The product is used for intra-operative nerve monitoring during surgery.
Identify the model number 5140-508-240 and serial number starting with 07613327177329.
The recall states the device may not optimally address usability issues, which could lead to use errors potentially causing nerve injury. It is not recommended for use without checking the recall.
The recall does not specify a remedy, so no action is required beyond checking if your device matches the model and serial numbers listed.
Check for the model number 5140-508-240 and serial number starting with 07613327177329. The product is used for intra-operative nerve monitoring during surgery.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0023-2020 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0023-2020 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.
