FDAFDA · Food and drugs·Recall number Z-0347-2018
Trevo XP ProVue System kit containing 1) Trevo XP ProVue Retriever, 4x20mm and 2) Trevo Pro18 Microcatheter
Published January 24, 2018 · Recall initiated: November 28, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Stryker Neurovascular has become aware that at least 1 (one) Trevo XP Provue System was manufactured where the carton sleeve did not match the physical contents of the pack.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Stryker Neurovascular
- Distributor
- OUS only - NL, FR, IT, DE, BE
- Lot
- UPN/Model No. 80052; Lot 63034
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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