GE Healthcare, LLC recalls Precision 500D
Recalled Product
Precision 500D
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 00000034206YY3 229353TR2 00000146304MO1 423778ERM4 Not Available 817255NHPD1
View official government recall
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