FDA Device recall Z-0914-2017
Prestilix
- FDA Device
- Class II
- terminated
- Published 2017-01-04
On 2017-01-04 the FDA classified a Class II recall of Prestilix by Ge Healthcare, citing GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0914-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-11-21 |
| Published | 2017-01-04 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ge Healthcare |
| Distribution | AL, AR, AZ, CA, CO, CT, DC, FL, GA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, PA, RI, SC, SD, TN, TX, VA, WA, WV, WY |
Product
Prestilix
Reason
GE Healthcare is conducting a recall due to the potential fall of aged CRT monitors - Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX and Innova 2000 systems.
Identifiers
| code_info | Mfg. Lot or Serial # System ID Not Available 1301 Not Available 318783ARF Not Available 412488F1 Not Available AP30…Mfg. Lot or Serial # System ID Not Available 1301 Not Available 318783ARF Not Available 412488F1 Not Available AP3001XR10 Not Available 902567GI Not Available C4211004 00000048037YY6 PC7281XR02 Not Available PC0731XR01 Not Available A5816801 00000022153YY1 C5304806 00000023739YY6 PL1020RX01 Not Available RU1146RX01 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0914-2017%22
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