MedSource Catheters MS-86220Recalls & reported problems
Medsource International LLC · ClearSafe Comfort Blood Control 20G x 1.25” · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 00840155409248), received between Feb 27, 2026 and Feb 27, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Separation” (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
- Material Separation1
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.
MalfunctionFeb 27, 2026Material Separation
THE NEEDLE COMPLETELY BROKE AWAY FROM THE HUB. THE NEEDLE WAS LEFT INSIDE THE PLASTIC CATHETER INSIDE THE PATIENT. PERSONNEL WAS ABLE TO RETRIEVE THE NEEDLE AFTER NOTICING THE PROBLEM. THE PATIENT WAS NOT HARMED. THE PATIENT AND THE TRUCK WERE BOTH STILL WHILE THIS HAPPENED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24475901 ↗
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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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