FDA Device recall Z-0909-2017
Legacy
- FDA Device
- Class II
- terminated
- Published 2017-01-04
On 2017-01-04 the FDA classified a Class II recall of Legacy 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-0909-2017 |
| 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
Legacy
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 00000118203MO9 256235ORF1 00000118220MO3 256235ORF2 00000100096MO7 205655LRF 0000008…Mfg. Lot or Serial # System ID 00000118203MO9 256235ORF1 00000118220MO3 256235ORF2 00000100096MO7 205655LRF 00000080072YY2 205783LRF2 00000119875MO3 205930LRF Not Available 205801KRF4 00000026146YY1 205793FLEG 00000047927YY9 205793FR1 00000089624MO1 205877LRF2 00000047907YY1 205534RM2 00000094699MO6 256517EF2 00000089628MO2 256534RM1 00000113953MO4 205387LRF 00000034291YY5 334293JLD3 00000063480YY8 256386LD1 00000063481YY6 256386LD2 00000119881MO1 205345RF3 00000119916MO5 205554VAL 00000128623MO6 479553RF2 00000118229MO4 501520RF1 00000100110MO6 501622SJR4 00000071209YY1 501751NWX2 00000146291MO0 520432RM1 00000063528YY4 480264RF1 00000119856MO3 480821RM2 00000119873MO8 480821RM2 00000128466MO0 928729RM4 00000128464MO5 928729RM5 00000071297YY6 602588LEGACY 00000128589MO9 602588ROOM5 00000063529YY2 602856LEG 00000063617YY5 602835RM2 00000118196MO5 602835RM3 00000118194MO0 602239RMF 00000063638YY1 602879RM1 00000128507MO1 623445LEG 00000119871MO2 6238 |
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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-0909-2017%22
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