GE Healthcare, LLC: Medical Device Recall in 2017 - (Recall #: Z-0910-2017)

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:

Precision 500D

Product Classification:

Class II

Date Initiated: November 21, 2016

Date Posted: January 4, 2017

Recall Number: Z-0910-2017

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 00000034206YY3 229353TR2 00000146304MO1 423778ERM4 Not Available 817255NHPD1

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