Digital Mobile X-ray Systems used to take diagnostic radiographic… — Class II medical device recall Z-1064-2015
Terminated recall by Virtual Imaging, Inc., reported 2015-02-18, distributed nationwide. There is a potential for unintended and erratic motion.
| Recall number | Z-1064-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Virtual Imaging, Inc., Boca Raton, FL, United States |
| Recall initiated | 2014-09-22 |
| Classified | 2015-02-09 |
| Reported by FDA | 2015-02-18 |
| Terminated | 2018-02-20 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, KR |
| Serial numbers | 60597, G-33634, G-35429, G-60069, G29393, G29395, G29404, G29416, G29426, G29824, G29864, G29873, G29878, G30025, G30155, G30156, G30160, G30165, G30173, G30236, G30240, G30250, G30254, G30258, G30567 and 287 more |
| Model numbers | 40KW, 50C, 55C, 55C/60C, 55G/60G, 70C, 80C, MOBILE2, MOBILE3, W/501C |
Product
Digital Mobile X-ray Systems used to take diagnostic radiographic exposures or patients.
Reason for recall
There is a potential for unintended and erratic motion.
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-1064-2015. 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.