Medline HCS3215Recalls & reported problems
Medline Industries, Inc. · CONNECTOR, PEDIATRIC, FLEX, 15MM X 15MM · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10888277190573), received between Aug 13, 2026 and Sep 13, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Crack” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Crack1
- Detachment of Device or Device Component1
- Material Fragmentation1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 13, 2026Material Fragmentation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50747676 ↗MalfunctionAug 13, 2026Crack; Detachment of Device or Device Component
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50235138 ↗
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- DAR 353S19046Covidien LP · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)1 recall1 report
- DAR 354/5876Covidien LP · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)25 reports
- AVANOS 93816Avanos Medical, Inc. · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)24 reports
- HUDSON RCI IPN040673Teleflex Incorporated · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)11 reports
- Portex 450952-NLIcu Medical, Inc. · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)8 reports
- Portex C45031682D-NLIcu Medical, Inc. · CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE)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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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