FDA Device recall Z-1448-2013
Philips Diagnost Stationary Radiographic System Models: 712020, 712022, 712050, 712052, 712055, 712057, 712062 Product Usage: Universal RAD…
- FDA Device
- Class II
- terminated
- Published 2013-06-26
On 2013-06-26 the FDA classified a Class II recall of Philips Diagnost Stationary Radiographic System Models: 712020, 712022, 712050, 712052, 712055, 712057, 712062 Product Usage: Universal RAD… by Philips Healthcare, citing installation Acceptance Test Document (IATD) non compliant with regulations. Records shows table height measurements out of specification with the consequence of potential system….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1448-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-01-16 |
| Published | 2013-06-26 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Philips Healthcare |
| Distribution | US |
Product
Philips Diagnost Stationary Radiographic System Models: 712020, 712022, 712050, 712052, 712055, 712057, 712062 Product Usage: Universal RAD Applications
Reason
Installation Acceptance Test Document (IATD) non compliant with regulations. Records shows table height measurements out of specification with the consequence of potential system mis-alignment.
Identifiers
| code_info | Serial numbers: 316235 335517 321739 334582 359767 357879 344896 351321 356953 365640 365639 359449 363674…Serial numbers: 316235 335517 321739 334582 359767 357879 344896 351321 356953 365640 365639 359449 363674 375601/SN0802006 368428 7272440 372848 373508 375366 396836/SN0802372 382140/SN0702475 381883/SN0802010 393931/SN0802399 396572/SN0802281 392502/SN0802179 390113/SN0802451 386784/SN0802264 381098/SN0802124 390098/SN0802242 382018/SN0802118 9000529 373499/SN0802249 383639/SN0802099 390129/SN0802521 404296/SN0802460 404298/SN0802474 416255/SN0902004 802119 409788/SN0802635 406492/SN0802489 390393/SN0802337 399024/SN0802562 402837/SN0802410 408716/SN0802551 408239/SN0802583 408240/SN0802630 408236/SN0802554 406024/SN0802481 408591 406156/SN0802537 406140/SN0802479 407675/SN0802517 408967/SN0802547 414087/SN08000100 435757/SN09000361 422092/SN0902023 415783/SN0802662 422536/SN09000199 416904/SN08000052 421962/SN09000054 429129/SN09000365 426287/SN09000096 430908/SN09000165 441638/SN09000356 456404/SN10000212 435210/SN09 |
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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-1448-2013%22
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