DeRoyal 71-C506Recalls & reported problems
Deroyal Industries, Inc. · Tubing Suction Connector · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00749756579032), received between Dec 5, 2024 and Jan 16, 2025 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Failure to Seal” (2 reports).
1 FDA recall record name this device's identifier, 1 still open.
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
Recalls naming this device
- Jan 15, 2025Open, Classified
The tubing may not ensure that the yankauer stays intact, and secure to the tubing / yankauer connection for a tight seal. This could result in inadequate suction and cause delay in patient care.
Z-1174-2025 · Root cause: Device Design · FDA record ↗
Most reported problems
Device problems
- Failure to Seal2
- Fitting Problem2
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- Insufficient Information1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 16, 2025Failure to Seal; Failure to Seal
A DISTRIBUTING FACILITY REPORTED, "THE CUSTOMER REPORTED THAT THEY HAVE HAD SEVERAL COMPLAINTS AND A SAFETY EVENT PUT IN THEIR SYSTEM ABOUT LOT# CNWKD04-06. THE GREEN END ON THIS LOT NUMBER IS WIDER AND NOT AS DEEP AS LOT NUMBER 19600504. IT WILL NOT STAY ATTACHED TO ANYTHING WHICH IS CAUSING ISSUES IN THEIR PICU".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21168136 ↗MalfunctionJan 15, 2025Fitting Problem; Fitting Problem
A USER FACILITY REPORTED, "TUBING DOES NOT FIT SECURELY ONTO THEIR ENDOSCOPES. THE 71-C506 DOES NOT STAY SECURE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21160088 ↗MalfunctionJan 8, 2025Failure to Seal; Failure to Seal
A USER FACILITY REPORTED, "THE SUCTION HANDLE WILL ONLY WORK/SEAL PROPERLY ON ONE END OF THE SUCTION TUBING. THE YANKEUR DOES NOT STAY ON AND THERE IS NO TIGHT SEAL. IT HAS BECOME A SAFETY ISSUE BECAUSE THEY NEED RAPID ACCESS TO RELIABLE SUCTION WITHOUT MISHAPS IN CONNECTIONS.".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21106358 ↗MalfunctionDec 5, 2024Fitting Problem; Fitting Problem
A USER FACILITY REPORTED, "SEVERAL COMPLAINTS AND A SAFETY EVENT PUT IN OUR SYSTEM ABOUT LOT# CNWKD04-06. THE GREEN END ON THIS LOT NUMBER IS WIDER AND NOT AS DEEP AS LOT NUMBER 19600504. IT WILL NOT STAY ATTACHED TO ANYTHING WHICH IS CAUSING ISSUES IN OUR PICU."
Patient problems: Insufficient Information
MAUDE report 20856652 ↗
Other TUBE, ASPIRATING, FLEXIBLE, CONNECTING devices
- DeRoyal 71-C512Deroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall2 reports
- DeRoyal 71-C520Deroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall1 report
- DeRoyal 71-C501Deroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall0 reports
- DeRoyal 71-C510Deroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall0 reports
- DeRoyal 71-C5100NSDeroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall0 reports
- DeRoyal 71-C6100NSDeroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall0 reports
- DeRoyal 71-C7100NSDeroyal Industries, Inc. · TUBE, ASPIRATING, FLEXIBLE, CONNECTING1 recall0 reports
- CONMED 0037860Conmed Corporation · TUBE, ASPIRATING, FLEXIBLE, CONNECTING20 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 · each recall links to the FDA recall notice
- 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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