FDA Device recall Z-0272-2018
3040-VenaFlow Calf Garment (Aircast) Quick Connect was mislabeled as 3010-PL Aircast Pos-Lock Connector
- FDA Device
- Class II
- terminated
- Published 2017-12-27
On 2017-12-27 the FDA classified a Class II recall of 3040-VenaFlow Calf Garment (Aircast) Quick Connect was mislabeled as 3010-PL Aircast Pos-Lock Connector by Stryker Sustainability Solutions, citing 3040 compression sleeves being mislabeled as a 3010-PL compression sleeves.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0272-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-12-01 |
| Published | 2017-12-27 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Stryker Sustainability Solutions |
| Distribution | TX |
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
3040 compression sleeves being mislabeled as a 3010-PL compression sleeves.
Identifiers
| code_info | Lot 6285035. UDI: 00885825016661. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0272-2018%22
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