GE Healthcare, LLC recalls Innova 2000
See all recalls from GE Healthcare, LLC →Recalled Product
Innova 2000
Hazard / Issue
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.
Issued by
FDA
Affected States: 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, WY, WV
Lot/Code Info: Mfg. Lot or Serial # System ID 00000063779YY3 303320CL2 00000063791YY8 312792RINOV2 00000128531M05 973365LAB1 00000063734YY8 312792GEMNET
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
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