3040-VenaFlow Calf Garment — Class II medical device recall Z-0272-2018
Terminated recall by Stryker Sustainability Solutions, reported 2017-12-27, distributed in TX. 3040 compression sleeves being mislabeled as a 3010-PL compression sleeves.
| Recall number | Z-0272-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Sustainability Solutions, Tempe, AZ, United States |
| Recall initiated | 2017-12-01 |
| Classified | 2017-12-21 |
| Reported by FDA | 2017-12-27 |
| Terminated | 2018-09-27 |
| Distributed | TX |
| Quantity | 280 devices |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00885825016661 |
| Lot numbers | 6285035 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0272-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.