# FDA recall Z-0272-2018

> **Stryker Sustainability Solutions** · Class II · device recall initiated 2017-12-01.

## Product

3040-VenaFlow Calf Garment (Aircast) Quick Connect was mislabeled as 3010-PL Aircast Pos-Lock Connector.    Intended for use in preventing deep vein thrombosis (DVT), diminishing post-operative pain and swelling, enhancing blood circulation and reducing wound healing time on the calf.

## Reason for recall

3040 compression sleeves being mislabeled as a 3010-PL compression sleeves.

## Distribution

Distributed to Texas.

## Key facts

- **Recall number:** Z-0272-2018
- **Recalling firm:** Stryker Sustainability Solutions
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-12-01
- **Report date:** 2017-12-27
- **Termination date:** 2018-09-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Tempe, AZ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0272-2018

## Citation

> AI Analytics. FDA recall Z-0272-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0272-2018. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*