FDA recall record

Stryker Neurovascular Trevo XP ProVue System kit containing 1) Trevo XP ProVue Retriever recall — FDA Z-0347-2018

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…

Class IIclassification
Z-0347-2018official record ID
Jan 24, 2018report date

Recall record at a glance

Official recordZ-0347-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmStryker Neurovascular
Report dateJan 24, 2018
Recall initiation dateNov 28, 2017
QuantityN/A
LocationFremont, CA, United States

Official product description

Trevo XP ProVue System kit containing 1) Trevo XP ProVue Retriever, 4x20mm and 2) Trevo Pro18 Microcatheter

Why the product was 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.

Distribution information

OUS only - NL, FR, IT, DE, BE

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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