McKesson 32647Recalls & reported problems
Mckesson Medical-Surgical Inc. · Oxygen Tubing CLEAR, 7’ (2.1 m) CRUSH RESISTANT | SINGLE PATIENT USE · Class 1
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20612479203758), received between Mar 14, 2024 and Mar 14, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Loose or Intermittent Connection” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Loose or Intermittent Connection1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 14, 2024Loose or Intermittent Connection; Loose or Intermittent Connection
OXYGEN TUBING PULLING OUT OF CONCENTRATOR CONNECTOR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18909185 ↗
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- O2 Tubing 001304USalter Labs · Tubing, Pressure And Accessories3 reports
- AirLife SO-1188-0Salter Labs · TUBING, PRESSURE AND ACCESSORIES3 reports
- AirLife 2025G-25Salter Labs · TUBING, PRESSURE AND ACCESSORIES2 reports
- Medline HCS4550GBMedline Industries, Inc. · TUBING, PRESSURE AND ACCESSORIES2 reports
- Flow sensor 155500Hamilton Medical AG · Tubing, Pressure And Accessories2 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.