RegWardenFDA facility compliance records
Facility

DELFI MEDICAL INNOVATIONS INC.

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)

  • Stocking, Medical Support (For General Medical Purposes)
    Product code FQL (opens in a new tab) · Class I · General Hospital · 21 CFR 880.5780

Recalls & enforcement

  • Class IITerminated2019-04-03
    Delfi Medical Innovations Inc has discovered that tourniquets cuffs in certain lots of the VariFit Sterile Single Use Thigh Cuffs, Single Port, Single Bladder models may have been manufactured with an inadequate perimeter weld on the cuff. Once applied to a patients thigh and in…

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. “DELFI MEDICAL INNOVATIONS INC. (FEI 3003748933) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3003748933-delfi-medical-innovations-inc/

Not open yet

Alerts for DELFI MEDICAL INNOVATIONS INC.

Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.

Planned

Want a one-page facility brief?

A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.