DeRoyal V71-1107Recalls & reported problems
Deroyal Industries, Inc. · SUCTION CANISTER, 2500cc, RIGID · 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 00749756603928), received between Mar 18, 2020 and Aug 20, 2020 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Material Integrity 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.
Most reported problems
Device problems
- Material Integrity Problem4
- Crack3
- Burst Container or Vessel1
Patient problems
- No Consequences Or Impact To Patient4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 20, 2020Crack; Material Integrity Problem; Crack; Material Integrity Problem
DURING A PROCEDURE, A CRACK WAS OBSERVED AT THE BOTTOM OF A SUCTION CAN.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10431549 ↗MalfunctionJul 1, 2020Crack; Material Integrity Problem; Crack; Material Integrity Problem
A SMALL CRACK WAS OBSERVED AT THE BOTTOM OF THE SUCTION CANISTER.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10217817 ↗MalfunctionJul 1, 2020Crack; Material Integrity Problem; Crack; Material Integrity Problem
THERE IS A CRACK AT THE BOTTOM OF THE SUCTION CAN. THE STAFF HAVE BEEN HEARING POPPING NOISES DURING PROCEDURES.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10217813 ↗MalfunctionMar 18, 2020Burst Container or Vessel; Material Integrity Problem; Burst Container or Vessel; Material Integrity Problem
THE CANISTER EXPLODED AND THE PIECES HIT STAFF MEMBERS. NO ONE WAS HURT. A SMALL AMOUNT OF FLUID WAS IN THE CANISTER. THE STAFF HAD TO CLEAN UP AND RESET UP THE SUCTION STAND.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9848215 ↗
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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