FDA Device recall Z-0911-2017
Prestige II
- FDA Device
- Class II
- terminated
- Published 2017-01-04
On 2017-01-04 the FDA classified a Class II recall of Prestige II 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-0911-2017 |
| 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
Prestige II
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 00000128555MO0 850526JR3 00000089643MO1 305227PRESTIGE1 00000094666MO5 305227PRESTIGE…Mfg. Lot or Serial # System ID 00000128555MO0 850526JR3 00000089643MO1 305227PRESTIGE1 00000094666MO5 305227PRESTIGE2 00000063792YY6 708216REM1 00000100104MO9 219416PRE 00000118238MO5 317338SVP 00000119906MO6 228314RF 00000113951MO8 662513RF2 Not Available 662513RF1 00000063697YY7 919472CGRFB 00000113961MO7 718262REM1 00000052137YY7 843692PRES 00000010115MO5 803778RF1 00000128514MO7 423493PRF4 Not Available 901226R9 Not Available 204623RF1 00000128614MO5 519685REM 00000063717YY3 905895RM3 00000113955MO9 905358REM 00000128544MO4 519631REM 00000128595MO6 326582XF1 00000063685YY2 082408040013 00000063685YY2 082408040013 00000063761YY1 082408100085 00000063716YY5 EG1024RX01 Not Available HDAR01XR02 00000128613MO7 IS1001RF01 00000063688YY6 A5181620 Not Available A5487204 00000063749YY6 B5130612 Not Available 0850080467 Not Available LY1006XR03 00000119921MO5 0853080154 00000063700YY9 0853080151 00000063700YY9 0853080151 00000119921MO5 0853080154 Not Avai |
|---|
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-0911-2017%22
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