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DAR 111P1160Recalls & reported problems

Covidien LP · 2-Way Exhalation Valve · Class 1

All models of DAR (35)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521100251), received between Nov 6, 2017 and Nov 6, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Device Operational Issue” (1 report).

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 16, 2026.

Most reported problems

Device problems

  • Device Operational Issue1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • InjuryNov 6, 2017Device Operational Issue; Device Operational Issue

    CUSTOMER REPORTED THE TAB/FLAP APPEARED TO HAVE BEEN BROKEN OFF ON E-VALVE. THE DEVICE WAS REPLACED. THERE WAS NO PATIENT INJURY OR ILL EFFECTS.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7005232 ↗

Other Circuit, Breathing (W Connector, Adaptor, Y Piece) devices

All Circuit, Breathing (W Connector, Adaptor, Y Piece) devices →

Sources and updates

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