FDA Device recall Z-0840-2013
STRYKER Sustainability Solutions, AC Power Adaptor for Restep Deep Vein Thrombosis (DVT) System, an external compression system
- FDA Device
- Class II
- terminated
- Published 2013-02-27
On 2013-02-27 the FDA classified a Class II recall of STRYKER Sustainability Solutions, AC Power Adaptor for Restep Deep Vein Thrombosis (DVT) System, an external compression system by Stryker Sustainability Solutions, citing reports that the AC Power Adaptor may not operate due to wires coming loose in the unit.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0840-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-08-30 |
| Published | 2013-02-27 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Stryker Sustainability Solutions |
| Distribution | AZ, NJ |
Product
STRYKER Sustainability Solutions, AC Power Adaptor for Restep Deep Vein Thrombosis (DVT) System, an external compression system. PUMPKIT (Pump Kit), and RSP159-01 (AC Power Adaptor).
Reason
Reports that the AC Power Adaptor may not operate due to wires coming loose in the unit.
Identifiers
| code_info | 108851407, 108851408, 108870192, 108874144, 108883271, 108886340, and 108888023. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0840-2013%22
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