McKesson 200-IVRWB201Recalls & reported problems
Mckesson Medical-Surgical Inc. · IV Catheter, Safety, Winged, Push button, Pink, 20G x 1" · Class 2
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 10612479268088), received between Jun 13, 2025 and Oct 29, 2025 — classified as 3 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
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.
MalfunctionOct 29, 2025Fail-Safe Problem; Fail-Safe Problem
THE CUSTOMER STATES THAT IF YOU PRESS THE END OF THE CATHETER ONCE RETRACTED YOU CAN STILL FEEL THE NEEDLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23417015 ↗MalfunctionJul 24, 2025Fail-Safe Problem; Fail-Safe Problem
IT WAS REPORTED BY THE CUSTOMER THAT WHEN THESE NEEDLES RETRACT, THEY ARE NOT STAYING RETRACTED. 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 22591298 ↗MalfunctionJun 13, 2025Fail-Safe Problem; Fail-Safe Problem
IT WAS REPORTED BY THE CUSTOMER THAT THE NEEDLE PROTRUDED WHEN THE DEVICE WAS TURNED UPSIDE DOWN AFTER RETRACTION. 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 22205171 ↗
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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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