Vital Signs™ 5108EXRecalls & reported problems
Airlife · Extension Set For Adult Anesthesia Breathing Circuit · Class 1
All models of Vital Signs (48)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10190752118775), received between Jan 1, 2026 and Jan 1, 2026 — classified as 2 injuries.
The most frequently reported specific device problem is “Loose or Intermittent Connection” (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. 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
- Loose or Intermittent Connection2
Patient problems
- Low Oxygen Saturation2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJan 1, 2026Loose or Intermittent Connection
SUNMED HOLDINGS LLC. RECEIVED A SINGLE REPORT THAT REFERENCED THREE DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING THREE DIFFERENT PATIENTS. THIS IS THE FIRST OF THREE REPORTS. REFER TO 1314417-2026-00002 FOR THE SECOND REPORT. REFER TO 2028807-2026-00001 FOR THE THIRD REPORT. IT WAS REPORTED, THE CIRCUIT DISCONNECTED MULTIPLE TIMES, WHICH HAS RESULTED IN THE PATIENT DESATURATING, DOWN INTO THE 60S. NO INFORMATION WAS PROVIDED CONCERNING MEDICAL INTERVENTION OR PATIENT OUTCOME.
Patient problems: Low Oxygen Saturation
MAUDE report 23940762 ↗InjuryJan 1, 2026Loose or Intermittent Connection
SUNMED HOLDINGS LLC. RECEIVED A SINGLE REPORT THAT REFERENCED THREE DIFFERENT INCIDENCES, WHICH WERE ASSOCIATED WITH SEPARATE UNITS, INVOLVING THREE DIFFERENT PATIENTS. THIS IS THE SECOND OF THREE REPORTS. REFER TO 1314417-2026-00001 FOR THE FIRST REPORT. REFER TO 2028807-2026-00001 FOR THE THIRD REPORT. IT WAS REPORTED, THE CIRCUIT DISCONNECTED MULTIPLE TIMES, WHICH HAS RESULTED IN THE PATIENT DESATURATING, DOWN INTO THE 60S. NO INFORMATION WAS PROVIDED CONCERNING MEDICAL INTERVENTION OR PATIENT OUTCOME.
Patient problems: Low Oxygen Saturation
MAUDE report 23940761 ↗
Other Circuit, breathing (w connector, adaptor, y piece) devices
- Medline Industries, Inc. DYNJ905503FMedline Industries, Inc. · Circuit, breathing (w connector, adaptor, y piece)3 recalls0 reports
- Medline Industries, Inc. PHS972096014BMedline Industries, Inc. · Circuit, breathing (w connector, adaptor, y piece)3 recalls0 reports
- Medline Industries, Inc. DYNJ0185290GMedline Industries, Inc. · Circuit, breathing (w connector, adaptor, y piece)3 recalls0 reports
- Medline Industries, Inc. DYNJ905503GMedline Industries, Inc. · Circuit, breathing (w connector, adaptor, y piece)2 recalls0 reports
- Medline Industries, Inc. DYNJAA262AMedline Industries, Inc. · Circuit, breathing (w connector, adaptor, y piece)2 recalls0 reports
- Medline Industries, Inc. DYNJ905567AMedline Industries, Inc. · Circuit, breathing (w connector, adaptor, y piece)2 recalls0 reports
- MEDLINE INDUSTRIES, INC. DYNJ86657AMedline Industries, Inc. · Circuit, breathing (w connector, adaptor, y piece)2 recalls0 reports
- Medline Industries, Inc. DYKMBNDL199AMedline Industries, Inc. · Circuit, breathing (w connector, adaptor, y piece)2 recalls0 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.
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