Dual Swivel Elbow with Suction Port MC-4475Recalls & reported problems
Medicomp · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00858409005344), received between Jun 14, 2024 and Jun 14, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Use of Device 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Use of Device Problem1
Patient problems
- Brain Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 14, 2024Use of Device Problem; Use of Device Problem
OUR INITIAL AND ONLY NOTIFICATION WAS ON APRIL 11, 2024 FROM THE LAW FIRM OF BEAUSAY & NICHOLS. THEIR LETTER STATED THE FOLLOWING: FOR STEVEN'S BRONCHOSCOPY, THE BRONCHOSCOPIST LTERALLY GOT THE BRONCHOSCOPE "STUCK" IN THE ADAPTER AND COULD NOT ADVANCE OR MANEUVER THE BRONCHOSCOPE, REQUIRING THAT HE REMOVE THE BRONCHOSCOPE AND ENDOTRACHEAL TUBE AS ONE UNIT. INTHE PROCESS OF THE BRONCHOSCOPE GETTING STUCK AND REMOVING THE ETT, STEVEN BEGAN DESATURATING AND EVENTUALLY ARRESTED. A CODE BLUE WAS INITIATED BUT STEVEN SUSTAINED A SEVERE ANOXIC BRAIN INJURY AS A RESULT OF THIS INCIDENT.
Patient problems: Brain Injury
MAUDE report 19537187 ↗
Other Connector, Airway (Extension) devices
- Flex Extenders 7-5132Westmed, Inc. · Connector, Airway (Extension)1 recall18 reports
- ErgoStar CM 55 MP01855Drägerwerk AG & Co. KGaA · Connector, Airway (Extension)1 recall10 reports
- ErgoStar CM 45 MP01845Drägerwerk AG & Co. KGaA · Connector, Airway (Extension)1 recall1 report
- ErgoStar CM 40 MP01840Drägerwerk AG & Co. KGaA · Connector, Airway (Extension)1 recall1 report
- Adaptors/Connectors S6411PWestmed, Inc. · Connector, Airway (Extension)1 recall0 reports
- Omnistream 011401Oridion Medical 1987 Ltd. · CONNECTOR, AIRWAY (EXTENSION)1 recall0 reports
- ErgoStar CM 60 MP01860Drägerwerk AG & Co. KGaA · Connector, Airway (Extension)1 recall0 reports
- Portex 66-1991Icu Medical, Inc. · CONNECTOR, AIRWAY (EXTENSION)8 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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page