Stryker recalls some Stroke Fast Packs and Trevo Procedure Packs due to mismatched carton labels and actual contents. Affected units may have incorrect items inside the packaging.
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 certain stroke intervention kits because the labels on the packaging don't match what's actually inside. This could lead to using the wrong medical devices during procedures.
The carton sleeve labels indicate different contents than what's actually inside the pack. This mismatch could cause healthcare workers to use incorrect medical devices during critical stroke procedures.
Healthcare professionals using these kits for stroke interventions may be affected. Patients receiving these kits are at risk if the wrong devices are used during procedures.
Check for the lot number QX10100894 on the carton sleeve. The product includes Trevo XP ProVue Procedure Packs, Trevo XP ProVUE Retriever, and Excelsior XT-27 1 TIP Straight.
Look for the lot number QX10100894 on the carton sleeve to identify affected units.
The recalled products are Trevo XP ProVue Procedure Packs, Trevo XP ProVUE Retriever, and Excelsior XT-27 1 TIP Straight with lot number QX10100894.
Check for the lot number QX10100894 on the carton sleeve. Affected units have mismatched labels and contents.
The recall record does not specify a remedy, so contact Stryker Neurovascular directly for guidance.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0277-2018 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0277-2018 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.
