Prime Series Stretchers — Class II medical device recall Z-1184-2016
Terminated recall by Stryker Medical Division of Stryker Corporation, reported 2016-03-23, distributed in AL, CA, DC, FL, MN, MT, NC, NE…. The hydraulic jack assemblies (PN: 0753-002-101, 0753-002-070, 0753-002-001, and 0753-002-001) were manufactur
| Recall number | Z-1184-2016 |
|---|---|
| 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 | 2016-02-05 |
| Classified | 2016-03-17 |
| Reported by FDA | 2016-03-23 |
| Terminated | 2016-09-06 |
| Distributed | AL, CA, DC, FL, MN, MT, NC, NE, NY, PA, RI, TN, TX, UT, WV |
| Quantity | 36 |
| Reason classes | packaging |
| Model numbers | 0753-002-001, 0753-002-070, 0753-002-101 |
Product
Prime Series Stretchers (Fifth Wheel, Big Wheel and Zoom) Powered stretcher
Reason for recall
The hydraulic jack assemblies (PN: 0753-002-101, 0753-002-070, 0753-002-001, and 0753-002-001) were manufactured using the incorrect oil. The oil used does not contain the same wear resistance additives as the specified oils and therefore its use increases the potential for wear which may cause a leak event or jack drift. Testing was done to evaluate the jacks with incorrect oil and leak events we
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-1184-2016. 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.