Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2800-2017 — Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 20, Trevo Pro 18 Microcatheter, AXS Catalyst 060x132CM - US, UPN M0033PK42022001

U.S. FDA — Device Enforcement · United States · 2017-06-26 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2800-2017
Date of alert
2017-06-26
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Stryker Neurovascular
Product category
device
Product type
Devices
Reported risk: Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs were manufactured using a carton sleeve where the pre-printed contents on the back of the sleeve did not match the physical contents of the pack.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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