GE Healthcare, LLC: Medical Device Recall in 2017 - (Recall #: Z-0907-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

ADVANTX LCN+

Product Classification:

Class II

Date Initiated: November 21, 2016

Date Posted: January 4, 2017

Recall Number: Z-0907-2017

Event ID: 75851

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.

Status: Terminated

Product Quantity: Total for all products 1,598 (USA 824, OUS 774)

Code Information:

Mfg. Lot or Serial # System ID 00000089619MO1 205592MLC 00000089632MO4 205592MLC 00000052196YY3 601459LC 00000023729YY7 910343NHC1 00000031441YY9 603668CLC3 00000034211YY3 603668CLC3 00000034271YY7 973429CATH Not Available 215576LC2 Not Available 610250SC Not Available 0910062022 Not Available 0910062022 00000023777YY6 1025 00000026231YY1 3919-1 00000023841YY0 93162 00000023841YY0 93162 Not Available GOLD000540

Distribution Pattern:

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 Russia Saudi Arabia Serbia Sierra Leone Slovakia Spain Taiwan Thailand Turkey United Arab Emirates United Kingdom Venezuela Vietnam

Voluntary or Mandated:

Voluntary: Firm initiated