[Recalled] Brilliance iCT (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems. — The firm was notified that the failure of the UPS accessory devices used in con… | FDA 2015
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | Brilliance iCT (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems. |
|---|---|
| Brand / manufacturer | Philips Medical Systems (Cleveland) Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1768-2015 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 06 March 2015 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The firm was notified that the failure of the UPS accessory devices used in conjunction with Computed Tomography X-ray systems and Diagnostic Imaging systems. may result in battery acid leakage, overheating and/or emission of fumes.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Philips Medical Systems (Cleveland) Inc
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.