DeRoyal 71-1500BRRecalls & reported problems
Deroyal Industries, Inc. · SafeLiner Outer Shell Suction Canister · Class 2
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00749756664660), received between Apr 27, 2026 and Apr 27, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fitting Problem” (1 report).
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
- Fitting Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 27, 2026Fitting Problem
A DISTRIBUTING FACILITY REPORTED, "TRIAL OF NEW PRODUCT SHOWS PRODUCT CANT BE USED APPROPRIATELY. THE SUCTION CANISTER TIP DOES NOT FIT INTO THE SUCTION SYSTEM. DURING A PROCEDURE WHERE QUICK SUCTIONING NEEDS TO BE PERFORMED, THE UNIT WILL FAIL TO PROVIDE SUCTION AND SUCTIONED CONTENTS WILL SPILL OR SPRAY ON CAREGIVERS, THE PATIENT, AND THE STERILE OPERATING/PROCEDURE AREA."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25003188 ↗
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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.