Precision 500D
Reported: January 4, 2017 Initiated: November 21, 2016 #Z-0910-2017
Product Description
Precision 500D
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.
Details
- Recalling Firm
- GE Healthcare, LLC
- Units Affected
- Total for all products 1,598 (USA 824, OUS 774)
- 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 Russia Saudi Arabia Serbia Sierra Leone Slovakia Spain Taiwan Thailand Turkey United Arab Emirates United Kingdom Venezuela Vietnam
- Location
- Waukesha, WI
Frequently Asked Questions
What product was recalled? ▼
Precision 500D. Recalled by GE Healthcare, LLC. Units affected: Total for all products 1,598 (USA 824, OUS 774).
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 4, 2017. Severity: Moderate. Recall number: Z-0910-2017.
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