Vital Signs™ 1552017 (UDI 10889483573631)Recalls & reported problems
Airlife · Vital Signs™ Pediatric 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
- 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 10889483573631), received between Jun 27, 2025 and Jun 27, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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
- Break1
- Material Fragmentation1
Patient problems
- Low Oxygen Saturation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 27, 2025Break; Material Fragmentation; Break; Material Fragmentation
THE PT DESATURATED TO LESS THAN 10% AND AS THE TEAM TRIED BAG VENTILATE THE CIRCUIT CONTINUED TO FELL APART IN MULTIPLE DIFFERENT PLACES. AFTER THE TEAM MANAGED TO STABILIZE THE INFANT, THEY WERE UNABLE TO CAPTURE C02 BECAUSE OF THE SINGLE, DISTAL, AND C02 PORT.
Patient problems: Low Oxygen Saturation
MAUDE report 22350429 ↗
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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