Reported Jan 4, 2017 · Terminated

Prestige VH

GE Healthcare, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: GE Healthcare, LLC · 3000 N Grandview Blvd · Waukesha, WI · 53188-1615

Is this the product you have?

  • Prestige VH
Lot codes and dates
  • Mfg. Lot or Serial # System ID Not Available
    • 708425PREST
    • 00000063646YY4
    • 314525APR
    • 00000034238YY6
    • 910249LRF3
    • 00000023833YY7
    • 919472CGRFA
    • 00000063653YY0
    • 724284R4
    • 00000052120YY3
    • 713442KPDRS
    • 00000063577YY1
    • 509458DR10
    • 00000048069YY9
    • AH4317XR04
    • 00000052117YY9
    • AH3221XR06
    • 00000026253YY5
    • AH5681XR02
    Not Available CS1029RX01 00000113920MO3 EG1112RX05 00000023862YY6 M4159446 00000034208YY9 M4160037 Not Available M1875113 00000039660YY6 M4500608 00000048049YY1 M2880713 00000026209YY7 M4046528 Not Available M2838405 Not Available
    • M2663805
    • 00000089618MO3
    • M4202921
    • 00000031488YY0
    • M9624214
    • 00000023814YY7
    • M4496929
    • 00000023829YY5
    • M4496929
    Not Available
    • B4192927
    • 00000034269YY1
    • HC2834XR11
    • 00000063668YY8
    • HC1627XR14
    • 00000026202YY2
    • HC0393XR02
    • 00000023796YY6
    • HC0760XR01
    • 00000026216YY2
    • PC0545XR04
    Not Available 490314XR02 Not Available MC5880XR03 Not Available CC2149XR02 Not Available IS1002RX01 00000063686YY0 IE1012RX03 00000063667YY0 IE1025RX02 Not Available IE1006RX07 00000063609YY2 A5250603 Not Available A5127805 00000034283YY2 NO1004RX01 00000026203YY0 NO1041RX01 Not Available
    • NO1104RX01
    • 00000048004YY6
    • NO1016RX02
    • 00000080076YY3
    • PPR00132
    • 00000063713YY2
    • PPR59013
    • 00000026248YY5
    • RU1306RX01
    • 00000063560YY7
    • CE165306
    • 00000063616YY7
    • 05074FLU02
    • 00000063755YY3
    • 38853103XRMET
Amount recalled
Total for all products 1,598 (USA 824, OUS 774)

This recall covers 13 products

The agency filed one notice per product. You are reading one of them; the other 12 are below.

Where it was sold

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Sep 26, 2017 · Data as of Sep 19, 5:33 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.