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Medical Device

Philips IntraSight Plus REF: 797423 and 797417 100-120v-220-240v,50/60hZ, 1000 VA

Recall date: 2026-10-07 · Source: FDA_DEVICE
Brand / Firm
Volcano Corp
Product
Philips IntraSight Plus REF: 797423 and 797417 100-120v-220-240v,50/60hZ, 1000 VA
Reason for recall
Software system may associate image data from one patient with another patient's record, potentially resulting in incorrect diagnosis or treatment.
Units affected
19 systems
Description
Philips IntraSight Plus REF: 797423 and 797417 100-120v-220-240v,50/60hZ, 1000 VA
View official recall notice →