GE Healthcare, LLC: Legacy

Is my product affected?

Legacy

• UPC 00000031365770

Check against the official notice below — it lists the full affected range.

What happened

GE Healthcare is recalling aged CRT monitors used in medical imaging systems including Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy, Precision 500D, ADVANTX, and Innova 2000 systems due to the potential for the monitors to fall. A total of 1,598 affected systems have been distributed across the United States and numerous countries overseas, including locations in Alabama, Arizona, California, Florida, New York, Texas, Canada, Japan, Australia, and many others.

The record does not specify a remedy or recommended course of action for affected consumers.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

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.

Details from the source

Reason for recall: 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. Distribution: US: 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, NY, NV, OH, OK, PA, RI, SC, SD, TN, TX,, VA, WA, WO, WY, WV. OUS: Algeria Armenia Australia Austria Brazil Canada Chile China Denmark Egypt France Germany Guatemala Honduras Hong Kong Hungary Iceland India Ireland Italy Japan Korea Libya Mexico Netherlands Netherlands Peru Poland Portugal Quantity: Total for all products 1,598 (USA 824, OUS 774) Lot/code info: 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 623879RM3 00000071252YY1 602994DRS 00000094664MO0 520742LEGACY 00000071291YY9 520742RM1 00000119898MO5 520872RM3 00000023695YY0 619242RF3 00000100087MO6 209386ATWRF 00000063549YY0 661282XR 00000063581YY3 650696M6 00000071217YY4 619725RM4 00000146295MO1 818884LRF1 00000063461YY8 916537MXF Not Available 209992CP1 00000026093YY5 818331SFX 00000023850YY1 707443JR5 00000022135YY8 209221TCX 00000100070MO2 831395RF2 00000153568M01 858626RF6 00000153565M07 858626RF7 00000128636MO8 925734RF1 00000113872MO6 RADNETRF130 00000063584YY7 323669ADV 0

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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