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AViD Dual Stage Venous Drainage Cannula TF293702ARecalls & reported problems

Edwards Lifesciences LLC · AVID DUAL STAGE VENOUS DRAINAGE CANNULA · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00690103161878), received between Feb 3, 2023 and Feb 3, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Markings/Labelling Problem” (1 report).

4 other recalls cover devices cleared under the same FDA submission (K120072); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Device Markings/Labelling Problem1
  • Incorrect Measurement1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionFeb 3, 2023Incorrect Measurement; Device Markings/Labelling Problem; Incorrect Measurement; Device Markings/Labelling Problem

    PER IMAGING EVALUATION REPORT OF TF293702A DUAL-STAGE VENOUS CANNULA'S MARKINGS ARE OFF WAS UNABLE TO BE CONFIRMED. TWO IMAGES WERE PROVIDED. FIRST IMAGE SHOWED A CANNULA FROM REPORTED MODEL ON TOP OF THE TYVEK LID FROM REPORTED MODEL AND LOT NUMBER. SECOND IMAGE SHOWED TWO CANNULAS INSIDE THE POUCH. LOCATION OF DEPTH MARKERS WAS NOT ABLE TO BE CONFIRMED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16294531 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K120072. One submission often covers many models, so check the product and lot details in each record.

  • Z-3029-2018 · Mar 7, 2018 · Terminated
    Edwards Lifesciences Thin-Flex Single Stage Venous Drainage Cannula, 38FRX40CM, resterilized.
  • Z-3031-2018 · Mar 7, 2018 · Terminated
    Edwards Lifesciences Avid Dual Stage Venous Drainage Cannula, 29/37F (9.6/12.3MM) X 37CM (14.5"), resterilized.
  • Z-3030-2018 · Mar 7, 2018 · Terminated
    Edwards Lifesciences Thin-Flex Single Stage Venous Drainage Cannula, 34F (11.3MM) X 40CM (16"), resterilized.
  • Z-0398-2016 · Nov 4, 2015 · Terminated
    Thin-Flex Venous Cannula, Model Number:TF292902A

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Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page