McKesson 200-IVRWB2434Recalls & reported problems
Mckesson Medical-Surgical Inc. · IV Catheter, Safety, Winged, Push button, Yellow, 24G x 3/4" · Class 2
Data updated Oct 18, 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 10612479268149), received between Mar 9, 2026 and Jun 12, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Activation Failure” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Activation Failure1
- Fail-Safe Did Not Operate1
- Fail-Safe Problem1
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.
MalfunctionJun 12, 2026Activation Failure; Fail-Safe Did Not Operate
IT WAS REPORTED BY THE CUSTOMER THAT THE NEEDLE IS NOT RETRACTING PROPERLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25491418 ↗MalfunctionMar 9, 2026Fail-Safe Problem
IT WAS REPORTED BY THE CUSTOMER THAT THE NEEDLE IS NOT RETRACTING PROPERLY. NO OTHER INFORMATION WAS RECEIVED REGARDING ANY SERIOUS INJURY AS A RESULT OF THIS PRODUCT ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24547230 ↗
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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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