DeRoyal V71-6510Recalls & reported problems
Deroyal Industries, Inc. · SUCTION CANISTER, 1000cc · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00749756728980), received between Dec 6, 2024 and Dec 6, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Suction Problem” (2 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 Problem2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 6, 2024Suction Problem; Suction Problem
A USER FACILITY REPORTED, "PRIOR TO INTUBATION, THE DECISION WAS MADE TO PLACE A NGT (NASOGASTRIC TUBE). NGT PLACED TO SUCTION. THERE WERE DIFFICULTIES GETTING THE SUCTION TO WORK. PATIENT INTUBATED. RN (REGISTERED NURSE) WAS ABLE TO GET SUCTION TO WORK AND LARGE VOLUME OF BLACK LIQUID SUCTIONED. IT WAS NOTED THE KEY ON THE SIDE OF THE SUCTION HOLDER WAS HORIZONTAL (SUCTION WAS OFF) AND ONCE THE KEY WAS TURNED VERTICAL, IT WAS FUNCTIONAL."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20867995 ↗MalfunctionDec 6, 2024Suction Problem; Suction Problem
A USER FACILITY REPORTED, "THE DEROYAL SUCTION CANISTER LINERS ARE EXPERIENCING ISSUES WITH SUCTION DUE TO FAULTY ADHESIVES BEING APPLIED. THE END USER MUST PRESS FIRMLY WHEN CONNECTING THE LID TO THE LINER. IF THE ADHESIVE DOESN'T CONNECT ALL THE WAY AROUND, THE SUCTION WILL NOT WORK. THERE ARE ISSUES WITH THE SUCTION DECREASING AND FAILING INTERMITTENT SUCTION. IN BOTH CASES, THE ISSUE IS FIXED BY BEING EXTRA FIRM WHEN CONNECTING THE LID TO THE LINER BEFORE PLACING IT IN THE CANISTER. DEROYAL ROUNDED, TOOK NOTES AND PICTURES AND WILL BE REPORTING BACK ASAP."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20867159 ↗
Other BOTTLE, COLLECTION, VACUUM devices
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- 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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