Class II — Sun Nuclear Corporation
| Recalling firm | SUN NUCLEAR CORPORATION |
|---|---|
| Registered facility | SUN NUCLEAR CORPORATION (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Has a Potential Pinch Hazard to user performing Machine QA in an MRI environment. |
| Product | IC PROFILER-MR - Model 1123. A radiologic quality assurance instrument is a device intended for medical purposes to measure a physical characteristic associated with another radiologic device. |
| Quantity | 6 Units. |
| Distribution | Distributed in the states of CA, CO, and OH. |
| Initiated | 2014-08-08 |
| Classified | 2015-01-13 |
| Terminated | 2015-03-23 |
| Recall number | Z-0959-2015 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Sun Nuclear Corporation (Z-0959-2015).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/69751/
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