Stryker SmartLife Large Aseptic Housing — Class II medical device recall Z-1886-2017
Terminated recall by Stryker Instruments Div. of Stryker Corporation, reported 2017-05-03. Stryker Instruments issued a notice of correction for an update to cleaning practices for the Stryker SmartLif
| Recall number | Z-1886-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Instruments Div. of Stryker Corporation, Portage, MI, United States |
| Recall initiated | 2017-02-28 |
| Classified | 2017-04-27 |
| Reported by FDA | 2017-05-03 |
| Terminated | 2023-01-23 |
| Countries outside the US | DE, FR |
| Quantity | 302 |
Product
Stryker SmartLife Large Aseptic Housing (7126-120-000)
Reason for recall
Stryker Instruments issued a notice of correction for an update to cleaning practices for the Stryker SmartLife Large Aseptic Housings following complaints of deterioration to the housing and the top and bottom housing separating at the weld. Using cleaning practices outside of the HIFU could lead to housing separating at the weld.
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-1886-2017. 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.