# FDA recall Z-2802-2017

> **Stryker Neurovascular** · Class II · device recall initiated 2017-06-26.

## Product

Stroke Fast Pack(TM) Trevo XP ProVue Retriever 6 x 25, AXS Catalyst 060x132CM - US, EXCELSIOR XT 27 MICROCATHETER, UPN M0033PK62523001  ST 150

## Reason for recall

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.

## Distribution

nationwide

## Key facts

- **Recall number:** Z-2802-2017
- **Recalling firm:** Stryker Neurovascular
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-06-26
- **Report date:** 2017-08-09
- **Termination date:** 2021-03-29

- **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-2802-2017

## Citation

> AI Analytics. FDA recall Z-2802-2017. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/Z-2802-2017. Source: US FDA. Licensed CC0.

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