DeRoyal V71-6530Recalls & reported problems
Deroyal Industries, Inc. · SUCTION CANISTER, 3000cc · Class 2
- 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 00749756728966), received between Aug 20, 2020 and Aug 27, 2020 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Filtration 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.
Most reported problems
Device problems
- Filtration Problem2
- Infusion or Flow Problem2
Patient problems
- No Consequences Or Impact To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 27, 2020Filtration Problem; Infusion or Flow Problem; Filtration Problem; Infusion or Flow Problem
DURING USE OF A SUCTION CANISTER, FLUID BACKFLOWED INTO THE HOSPITAL VACUUM SYSTEM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10459412 ↗MalfunctionAug 20, 2020Filtration Problem; Infusion or Flow Problem; Filtration Problem; Infusion or Flow Problem
DURING USE OF A SUCTION CANISTER, FLUID BACKFLOWED INTO THE HOSPITAL VACUUM SYSTEM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10431550 ↗
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- Medline DYNDSCL1500Medline Industries, Inc. · BOTTLE, COLLECTION, VACUUM1 recall13 reports
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.