McKesson 200-IVRB2434Recalls & reported problems
Mckesson Medical-Surgical Inc. · IV Catheter, Safety, Push button, Yellow, 24G x 3/4" · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10612479268057), received between Apr 24, 2025 and Apr 29, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Fail-Safe Problem” (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.
Reports received per month
Most reported problems
Device problems
- Fail-Safe Problem3
- Fail-Safe Did Not Operate1
- Physical Resistance/Sticking1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 29, 2026Physical Resistance/Sticking; Fail-Safe Did Not Operate
THE CATHETER STICKS WHEN ADVANCING THE CATHETER/STRAW OFF THE NEEDLE DURING IV START. THE CATHETER ALSO STICKS WHEN THE NEEDLE RETRACTION BUTTON IS PRESSED, WHICH HAS LED TO TWO PRIMARY CONCERNS: THE FORCE OF THE RETRACTION CAN PULL THE CATHETER OUT OF THE VEIN, REQUIRING THE PATIENT TO UNDERGO A SECOND IV INSERTION. IN SOME CASES, THE NEEDLE DOES NOT RETRACT, REQUIRING THE CLINICIAN TO MANUALLY REMOVE THE NEEDLE, WHICH INCREASES THE RISK OF ACCIDENTAL NEEDLE STICK OR EXPOSURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25036044 ↗MalfunctionSep 3, 2025Fail-Safe Problem; Fail-Safe Problem
IT WAS REPORTED BY THE CUSTOMER THAT THE CATHETERS ARE NOT RETRACTING AFTER USE. NO INFORMATION WAS RECEIVED REGARDING ANY SERIOUS INJURY AS A RESULT OF THIS PRODUCT ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22951879 ↗MalfunctionSep 3, 2025Fail-Safe Problem; Fail-Safe Problem
IT WAS REPORTED BY THE CUSTOMER THAT THE CATHETERS ARE NOT RETRACTING AFTER USE. NO INFORMATION WAS RECEIVED REGARDING ANY SERIOUS INJURY AS A RESULT OF THIS PRODUCT ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22951317 ↗MalfunctionApr 24, 2025Fail-Safe Problem; Fail-Safe Problem
IT WAS REPORTED BY THE CUSTOMER THAT THE SAFETY FEATURE IS FAULTY AND THE NEEDLE COMES OUT SLIGHTLY IF YOU TURN THE CATHETER. NO INFORMATION WAS RECEIVED REGARDING ANY SERIOUS INJURY AS A RESULT OF THIS PRODUCT ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21900053 ↗
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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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