Stryker Neurovascular recalls specific Trevo XP ProVue Retriever models due to potential endotoxin levels exceeding safety standards, which may cause fever, shock, or aseptic meningitis.
Neurovascular devices did not meet the minimum sample size required for endotoxin testing during manufacturing processes and are out of compliance with the AAMI ST72 standard, so these devices may exceed the acceptable limits of endotoxin levels; high levels of endotoxins may increase the risk of fever, shock and aseptic meningitis.
Stryker is recalling certain Trevo XP ProVue Retriever surgical devices because they may have unsafe levels of endotoxins that could lead to fever, shock, or aseptic meningitis. These devices were made without meeting endotoxin testing standards.
These devices failed endotoxin testing during manufacturing, which means they might contain higher levels of endotoxins than allowed. Endotoxins can cause fever, shock, or aseptic meningitis in patients during surgery.
Healthcare professionals using these specific Trevo XP ProVue Retriever models in surgical procedures are most at risk. Patients receiving these devices during surgery may experience complications.
Check for the product names and catalog numbers listed in the recall notice: Trevo XP ProVue Retriever 4 x 20 (Catalog 90182), Trevo XP ProVue Retriever 3 x 20 (Catalog 90183), and other specific models with their associated catalog numbers.
Identify if your device matches the recalled models and catalog numbers listed in the recall notice.
The devices did not meet the minimum sample size required for endotoxin testing during manufacturing, leading to potential endotoxin levels exceeding safety standards.
High endotoxin levels may cause fever, shock, or aseptic meningitis in patients during surgery.
Check for the specific product names and catalog numbers listed in the recall notice, such as Trevo XP ProVue Retriever 4 x 20 (Catalog 90182) or Trevo XP ProVue Retriever 3 x 20 (Catalog 90183).
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-1902-2024 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-1902-2024 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.
