Delfi Medical Innovations, Inc. Recalls

Overview of recall records associated with Delfi Medical Innovations, Inc., including dates, categories and classifications where available.

2recall records

May 13, 2020latest record date

May 13, 2020earliest record date

Recall history in this database

Classification mix: Class II: 2.

Medical DeviceMay 13, 2020

Delfi Medical Innovations, VariFit Contour Cuffs, single use adult thigh cuff, single port recall — FDA Z-1901-2020

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…

Class IIFDA: TerminatedDelfi Medical Innovations, Inc.

Medical DeviceMay 13, 2020

DELFI SINGLE USE VARIFIT TOURNIQUET CUFF SINGLE PORT SINGLE BLADDER CONTOUR THIGH CUFF WITH recall — FDA Z-1902-2020

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…

Class IIFDA: TerminatedDelfi Medical Innovations, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Delfi Medical Innovations, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.