Trevo XP ProVue System kit containing 1) Trevo XP ProVue Retriever, 4x20mm and 2) Trevo Pro18 Microcatheter
Reported: January 24, 2018 Initiated: November 28, 2017 #Z-0347-2018
Product Description
Trevo XP ProVue System kit containing 1) Trevo XP ProVue Retriever, 4x20mm and 2) Trevo Pro18 Microcatheter
Reason for Recall
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.
Details
- Recalling Firm
- Stryker Neurovascular
- Units Affected
- N/A
- Distribution
- OUS only - NL, FR, IT, DE, BE
- Location
- Fremont, CA
Frequently Asked Questions
What product was recalled? ▼
Trevo XP ProVue System kit containing 1) Trevo XP ProVue Retriever, 4x20mm and 2) Trevo Pro18 Microcatheter. Recalled by Stryker Neurovascular. Units affected: N/A.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 24, 2018. Severity: Moderate. Recall number: Z-0347-2018.
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