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 AvailableNot Available CS1029RX01 00000113920MO3 EG1112RX05 00000023862YY6 M4159446 00000034208YY9 M4160037 Not Available M1875113 00000039660YY6 M4500608 00000048049YY1 M2880713 00000026209YY7 M4046528 Not Available M2838405 Not Available
708425PREST00000063646YY4314525APR00000034238YY6910249LRF300000023833YY7919472CGRFA00000063653YY0724284R400000052120YY3713442KPDRS00000063577YY1509458DR1000000048069YY9AH4317XR0400000052117YY9AH3221XR0600000026253YY5AH5681XR02
Not AvailableM266380500000089618MO3M420292100000031488YY0M962421400000023814YY7M449692900000023829YY5M4496929
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 AvailableB419292700000034269YY1HC2834XR1100000063668YY8HC1627XR1400000026202YY2HC0393XR0200000023796YY6HC0760XR0100000026216YY2PC0545XR04
NO1104RX0100000048004YY6NO1016RX0200000080076YY3PPR0013200000063713YY2PPR5901300000026248YY5RU1306RX0100000063560YY7CE16530600000063616YY705074FLU0200000063755YY338853103XRMET
- Mfg. Lot or Serial # System ID Not Available
- 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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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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