# FDA recall Z-0276-2018

> **Stryker Neurovascular** · Class II · device recall initiated 2017-11-03.

## Product

Stroke Fast Pack(TM), Trevo(TM) XP, TREVO(TM) XP PROVUE RETRIEVER, 4 mm, 20 mm, ; Trevo(TM) Pro 18, TREVO PRO 18 MICROCATHETER, 0.021 in ID, 150 cm; AXS Catalyst(TM) 6,  Distal Access Catheter, 0.060 in, 132 cm; UPN M0033PK42022002    Stroke intervention kit

## Reason for recall

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.

## Distribution

International Distribution to: Germany, Slovakia and Israel.

## Key facts

- **Recall number:** Z-0276-2018
- **Recalling firm:** Stryker Neurovascular
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-11-03
- **Report date:** 2017-12-27
- **Termination date:** 2019-11-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Fremont, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0276-2018

## Citation

> AI Analytics. FDA recall Z-0276-2018. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0276-2018. Source: US FDA. Licensed CC0.

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