Stryker recalls specific models of Trevo XP ProVue Retriever due to increased risk of stent retriever separation from core wire during procedures, potentially leaving devices in vasculature. Affected units include certain sizes and reference numbers.
Increase in fracture complaints of the flexible, tapered core wire, resulting in stent retriever separation from the core wire during use. The stent retriever can be left behind in the vasculature.
Stryker is recalling specific models of Trevo XP ProVue Retriever devices because the flexible core wire can separate during use, potentially leaving the stent retriever inside blood vessels. This could cause serious complications for patients undergoing vascular procedures.
The flexible, tapered core wire in these devices can separate from the stent retriever during use, which may leave the stent retriever inside blood vessels. This could cause blockages or other complications if not properly removed.
Medical professionals using the Trevo XP ProVue Retriever during vascular procedures are most at risk. Patients who have recently received the recalled device may also be affected.
Check for the following reference numbers: 90182 (4MM x 20MM), 90185 (4MM x 30MM), or 90186 (6MM x 25MM). Also look for specific lot numbers and procedure pack references listed in the recall notice.
Verify the reference number on your device to see if it matches the recalled models listed in the recall notice.
Reach out to Stryker directly for guidance on next steps if your device is affected.
The recall indicates a risk of separation during use, so affected devices should not be used until contacted by Stryker for guidance.
Check the reference numbers and lot numbers listed in the recall notice to determine if your device is affected. Contact Stryker for further instructions.
No, affected devices should not be used until Stryker provides instructions on how to handle them safely.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0114-2021 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0114-2021 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.
