DeRoyal 71-1105Recalls & reported problems
Deroyal Industries, Inc. · SUCTION CANISTER, 1500cc, RIGID · Class 2
- 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 00749756049146), received between Jun 27, 2019 and Jun 27, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Infusion or Flow Problem” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Infusion or Flow Problem1
- Suction Problem1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 27, 2019Suction Problem; Infusion or Flow Problem; Suction Problem; Infusion or Flow Problem
DURING A BEDSIDE BRONCHOSCOPY, AN ISSUE WITH THE SUCTIONING DEVICE AROSE. THERE WAS NOT ADEQUATE SUCTION THROUGH THE SCOPE. WALL MOUNT WAS CHANGED, SCOPE WAS SWITCHED OUT, MULTIPLE CANISTERS WERE ALSO CHANGED. AFTER CONFIRMING THAT THE WALL SUCTION WAS ADEQUATE AND THE SCOPE IN WORKING ORDER, DR. NOTED THAT THE SUCTION AFTER THE CANISTER WAS NOT STRONG ENOUGH. THERE SEEMS TO BE AN INADEQUATE SEAL ON THE CURRENT CANISTERS TO ALLOW THE SUCTION TO WORK APPROPRIATELY. ANESTHESIA WAS IN THE ROOM AND HE STATED THAT THIS HAS OCCURRED MULTIPLE TIMES IN THE OR AS WELL. THOUGH THE PATIENT WAS NOT INJURED IN ANY WAY, THIS COULD HAVE POSED A SERIOUS THREAT IF THE PROCEDURE WAS MORE IN DEPTH.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8739173 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.