Stryker SmartLife Small Aseptic Housing REF 7222-120-000 Rx Only The… — Class II medical device recall Z-0173-2015
Terminated recall by Stryker Instruments Div. of Stryker Corporation, reported 2014-11-12, distributed nationwide. The SmartLife Aseptic Housings are being recalled in that the top section of the housing may separate from the
| Recall number | Z-0173-2015 |
|---|---|
| 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 | 2014-10-08 |
| Classified | 2014-11-05 |
| Reported by FDA | 2014-11-12 |
| Terminated | 2016-05-31 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, CH, FR, GB, HK, IN, JP, NL, PL, SE, ZA |
| Quantity | 3,138 in |
| Model numbers | 7222-120-000 |
Product
Stryker SmartLife Small Aseptic Housing REF 7222-120-000 Rx Only The SmartLife" Aseptic Housings are designed to be used in conjunction with the SmartLife Non-Sterile Batteries to provide power for System 7 Handpieces, Cordless Driver 4 Handpiece, and Sabo2 Sagittal Saw Handpiece.
Reason for recall
The SmartLife Aseptic Housings are being recalled in that the top section of the housing may separate from the bottom section due to insufficient welding.
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-0173-2015. 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.