Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1901-2020 — Delfi Medical Innovations, VariFit Contour Cuffs, single use adult thigh cuff, single port, single bladder, REF 9-9300-003. Rx Only, Sterile

U.S. FDA — Device Enforcement · Canada · 2019-04-03 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1901-2020
Date of alert
2019-04-03
Country / jurisdiction
Canada
Risk level
Class II
Risk type
recall
Brand
Delfi Medical Innovations, Inc.
Product category
device
Product type
Devices
Reported risk: 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 inflated to a pressure to occlude blood flow in the thigh distal to the cuff, after a period of time the cuff may leak to the extent that the tourniquet instrument supplying air pressure to the cuff may not be able to adequately control and regulate pressure in the cuff. This may result in some blood flow in the thigh distal to the cuff.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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