FDA Device recall Z-2494-2012
Philips Digital Diagnost with patient carriage Model: 712050 with serial number range from 00 000 00 to 09 000 543
- FDA Device
- Class II
- terminated
- Published 2012-10-10
On 2012-10-10 the FDA classified a Class II recall of Philips Digital Diagnost with patient carriage Model: 712050 with serial number range from 00 000 00 to 09 000 543 by Philips Healthcare, citing hook does not securely hold the footplate in vertical position, causing the footplate to disengage and may fall on patient or operator.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2494-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-09-12 |
| Published | 2012-10-10 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Philips Healthcare |
| Distribution | US |
Product
Philips Digital Diagnost with patient carriage Model: 712050 with serial number range from 00 000 00 to 09 000 543. Product Usage: Stationary radiographic System
Reason
Hook does not securely hold the footplate in vertical position, causing the footplate to disengage and may fall on patient or operator
Identifiers
| code_info | Serial number range (patient carriage) from: 00 000 00 to 09 000 543. |
|---|
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-2494-2012%22
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