STRYKER Sustainability Solutions — Class II medical device recall Z-0840-2013
Terminated recall by Stryker Sustainability Solutions, reported 2013-02-27, distributed in AZ, NJ. Reports that the AC Power Adaptor may not operate due to wires coming loose in the unit.
| Recall number | Z-0840-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Sustainability Solutions, Tempe, AZ, United States |
| Recall initiated | 2012-08-30 |
| Classified | 2013-02-20 |
| Reported by FDA | 2013-02-27 |
| Terminated | 2014-09-30 |
| Distributed | AZ, NJ |
| Quantity | 1,311 |
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 for recall
Reports that the AC Power Adaptor may not operate due to wires coming loose in the unit.
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-0840-2013. 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.