FDA Device recall Z-2366-2015
Oasis Coil Extension Cable used with Hitachi Oasis MRI System Product Usage: The Oasis MR system is an imaging device and is intended to pr…
- FDA Device
- Class II
- terminated
- Published 2015-08-19
On 2015-08-19 the FDA classified a Class II recall of Oasis Coil Extension Cable used with Hitachi Oasis MRI System Product Usage: The Oasis MR system is an imaging device and is intended to pr… by Hitachi Medical Systems America, citing the firm received a complaint stating the Coil Extension Cable accessory would overheat and be a burn hazard if touched.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2366-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-04-25 |
| Published | 2015-08-19 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Hitachi Medical Systems America |
| Distribution | US |
Product
Oasis Coil Extension Cable used with Hitachi Oasis MRI System Product Usage: The Oasis MR system is an imaging device and is intended to provide the physician with physiological and clinical information, obtained non-invasively and without the use of ionizing radiation. The Oasis system produces transverse, coronal, sagittal, oblique, and curved cross-sectional images that display the internal structure of the head, body, or extremities. The images produced by the MR systems reflect the spatial distribution of protons (hydrogen nuclei) exhibiting magnetic resonance. The NMR properties that determine the image appearance are proton density, spin-lattice relaxation time (T1), spin-spin relaxation time (T2), and flow. When interpreted by a trained physician, these images provide information that can be useful in diagnosis determination. The Coil Extension Cable that is the subject of the removal action is an accessory that is used in conjunction with certain anatomy coils to aid in patient positioning.
Reason
The firm received a complaint stating the Coil Extension Cable accessory would overheat and be a burn hazard if touched.
Identifiers
| code_info | Serial #'s: M001to M108, M110 to M175, M951 & M952. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2366-2015%22
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