The Stryker Model 6390 — Class II medical device recall Z-0566-2013
Terminated recall by Stryker Medical Division of Stryker Corporation, reported 2012-12-26, distributed nationwide. Model 6390 Power-LOAD systems built between September 12, 2012 and September 27, 2012 may have been built with
| Recall number | Z-0566-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Medical Division of Stryker Corporation, Portage, MI, United States |
| Recall initiated | 2012-10-11 |
| Classified | 2012-12-19 |
| Reported by FDA | 2012-12-26 |
| Terminated | 2013-08-30 |
| Distributed | Nationwide (US) |
| Quantity | 24 |
| Serial numbers | 120940203, 120940217, 120940257, 120940258, 120940259, 120940260, 120940261, 120940275, 120940276, 120940277, 120940290, 120940291, 120940292, 120940293, 120940294, 120940431, 120940435, 120940436, 120940437, 120940448, 120940449, 120940454, 120940458, 120940459 |
| Model numbers | 6390, 6390000000 |
Product
The Stryker Model 6390, Power-LOAD, is a power-loading cot fastener system designed to lift, lower, or steer ambulance cots into and out of the ambulance.
Reason for recall
Model 6390 Power-LOAD systems built between September 12, 2012 and September 27, 2012 may have been built with a load switch slide that does not meet specifications causing the lifting ability of the arms to be negatively impacted.
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-0566-2013. 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.