RegWardenFDA facility compliance records
Facility

Change Healthcare Israel Ltd.

1 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2019: 1 recalls20172018120192020202120222023202420252026
  • Recalls (1)

Devices registered here (1)

  • Computer, Diagnostic, Programmable
    Product code DQK (opens in a new tab) · Class II · Cardiovascular · 21 CFR 870.1425

Recalls & enforcement

  • Class IITerminated2019-03-25
    users are not notified of procedure medication discrepancies between the Vitals and Meds, the Procedure Notes and Patient Common Data screens in Horizon/McKesson Cardiology Hemo" (Hemo). The discrepancy may also affect administered medication data in reports generated from Hemo …

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Change Healthcare Israel Ltd. (FEI 3007784465) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3007784465-change-healthcare-israel-ltd/

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