DeRoyal 71-8003Recalls & reported problems
Deroyal Industries, Inc. · 1500cc Rigid Canister w/Elbow · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00749756375795), received between Aug 12, 2024 and Aug 28, 2024 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Suction Problem” (4 reports).
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.
Reports received per month
Most reported problems
Device problems
- Suction Problem4
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 28, 2024Suction Problem; Suction Problem
USER FACLITY REPORTED "WE HAD AN ISSUE TONIGHT AGAIN WHERE THE SUCTION WAS PREVIOUSLY WORKING EARLIER IN THE NIGHT AND SUDDENLY STOPPED AROUND 0200 THIS MORNING. "
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20084439 ↗MalfunctionAug 28, 2024Suction Problem; Suction Problem
USER FACLITY REPORTED "CANISTER WOULD NOT SUCTION; CHANGED THE CANISTER 2X UNTIL ONE WORKED; DISCARDED".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20084434 ↗MalfunctionAug 12, 2024Suction Problem; Suction Problem
A USER FACILITY REPORTED, "CANISTER WOULD NOT PROVIDE SUCTION. WHEN TUBING WAS FULL IT WOULD SHUT OFF".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19960645 ↗MalfunctionAug 12, 2024Suction Problem; Suction Problem
A USER FACILITY REPORTED, "CANISTER DOES NOT WORK TO PULL SUCTION DURING PROCEDURE. CHANGED CANISTER MULTIPLE TIMES AND SUCTION WOULD CEASE AFTER SHORT TIME".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19960621 ↗
Other BOTTLE, COLLECTION, VACUUM devices
- OASIS 3600-100Atrium Medical Corporation · Bottle, Collection, Vacuum3 recalls1 death175 reports
- OCEAN 2002-000Atrium Medical Corporation · BOTTLE, COLLECTION, VACUUM3 recalls44 reports
- EXPRESS 16400Atrium Medical Corporation · BOTTLE, COLLECTION, VACUUM1 recall110 reports
- EXPRESS 4000-100NAtrium Medical Corporation · Bottle, Collection, Vacuum2 recalls30 reports
- OCEAN 2002-400Atrium Medical Corporation · BOTTLE, COLLECTION, VACUUM2 recalls18 reports
- OASIS 3612-100Atrium Medical Corporation · Bottle, Collection, Vacuum1 recall18 reports
- Medline DYNDSCL1500Medline Industries, Inc. · BOTTLE, COLLECTION, VACUUM1 recall13 reports
- PNEUMOSTAT 16100Atrium Medical Corporation · BOTTLE, COLLECTION, VACUUM1 recall3 deaths12 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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