DeRoyal 71-1500DSBRecalls & reported problems
Deroyal Industries, Inc. · SafeLiner Outer Shell Suction Canister · 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 00749756675208), received between Oct 19, 2018 and Nov 1, 2018 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Collapse” (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
- Collapse2
- Mechanical Problem2
- Structural Problem2
Patient problems
- No Known Impact Or Consequence To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 1, 2018Collapse; Mechanical Problem; Structural Problem; Collapse; Mechanical Problem; Structural Problem
THE DISPOSABLE CANISTER LINERS ARE COLLAPSING DURING USE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8028786 ↗MalfunctionOct 19, 2018Collapse; Mechanical Problem; Structural Problem; Collapse; Mechanical Problem; Structural Problem
THE DISPOSABLE LINERS COLLAPSED DURING USE OF THE WASTE FLUID MANAGEMENT CANISTERS. FOR ONE OCCURRENCE, THE PHYSICIAN HAD TO USE PORTABLE SUCTION FROM THE CRASH CART.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7984806 ↗
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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