INTROCAN SAFETY® 4252520-020Recalls & reported problems
B. Braun Medical Inc. · INTROCAN SAFETY FEP 22G, 0.9X45MM -US · Class 2
All models of INTROCAN SAFETY (46)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 04046964399183), received between Aug 11, 2023 and Aug 11, 2023 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Break” (3 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.
Most reported problems
Device problems
- Break3
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 11, 2023Break; Break
AS REPORTED BY THE USER FACILITY: EVENT 1: DETAILED INQUIRY DESCRIPTION: CUSTOMER REPORTS THAT 3 INTROCAN SAFETY IV CATHETERS WERE BROKEN IN THE PACKAGING. THE PACKAGING WAS INTACT. CATHETERS WERE RETRIEVED FROM THE BOX. NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17509828 ↗MalfunctionAug 11, 2023Break; Break
AS REPORTED BY THE USER FACILITY: EVENT 2: DETAILED INQUIRY DESCRIPTION: CUSTOMER REPORTS THAT 3 INTROCAN SAFETY IV CATHETERS WERE BROKEN IN THE PACKAGING. THE PACKAGING WAS INTACT. CATHETERS WERE RETRIEVED FROM THE BOX. NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17509827 ↗MalfunctionAug 11, 2023Break; Break
AS REPORTED BY THE USER FACILITY: EVENT 3: DETAILED INQUIRY DESCRIPTION: CUSTOMER REPORTS THAT 3 INTROCAN SAFETY IV CATHETERS WERE BROKEN IN THE PACKAGING. THE PACKAGING WAS INTACT. CATHETERS WERE RETRIEVED FROM THE BOX. NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17509826 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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