Stryker recalls certain stroke intervention kits due to potential mismatch between carton labels and actual contents. Affected kits may contain incorrect components, risking improper use during medical procedures.
Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs and Trevo Procedure Packs were manufactured using a carton sleeve where the sleeve label contents did not match the physical contents within the pack.
Stryker is recalling specific stroke intervention kits that may have mismatched contents between the carton label and what's inside. This could lead to using the wrong components during critical medical procedures.
The carton label on the kit may not match the actual contents inside. This mismatch could lead to using the wrong components during stroke treatment procedures, potentially causing complications.
Healthcare professionals using the recalled stroke intervention kits are most at risk. Patients receiving these kits during procedures may be affected if the mismatch causes incorrect component use.
Check for the lot numbers QXC1020:0043 or QXC1020:0044 with expiration dates of August 28, 2018. The kits include specific stroke intervention components like the Stroke Fast Pack, Trevo XP, and Excelsior XT-27.
Compare the carton label with the actual contents to ensure they match. If they don't match, stop using the kit.
The affected kits include Stroke Fast Packs, Trevo XP, TREVO XP PROVUE RETRIEVER, 6 mm, 25 mm; Excelsior XT-27, MICROCATHETER, 150 cm, 6 cm; and AXS Catalyst 6, Distal Access Catheter, 0.060 in, 132 cm with lot numbers QXC10200043 or QXC10200044.
Look for lot numbers QXC10200043 or QXC10200044 with an expiration date of August 28, 2018 on the carton.
If the carton label does not match the contents, stop using the kit immediately and contact Stryker Neurovascular for further instructions.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0275-2018 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0275-2018 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.
