[Recalled] Philips Digital Diagnost-Mobile Detector Holder for Digital Diagnost (Single Detector, Dual Detector, Release 3) System codes: 712020, 712022, 712025 This system is used for making X-ray exposures for diagnostics. — The Wirel
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | Philips Digital Diagnost-Mobile Detector Holder for Digital Diagnost (Single Detector, Dual Detector, Release 3) System codes: 712020, 712022, 712025 This system is used for making X-ray exposures for diagnostics. |
|---|---|
| Brand / manufacturer | Philips Healthcare Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2465-2012 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 06 September 2012 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The Wireless Portable Detector (WPD) is not fixed securely inside the Mobile Detector Holder and may fall down
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 Healthcare 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.
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