McKesson 200-IVRWB221Recalls & reported problems
Mckesson Medical-Surgical Inc. · IV Catheter, Safety, Winged, Push button, Blue, 22G x 1" · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10612479268118), received between May 29, 2025 and Dec 9, 2025 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Fail-Safe Problem” (5 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Fail-Safe Problem5
- Partial Blockage1
Patient problems
- No Clinical Signs, Symptoms or Conditions6
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 9, 2025Partial Blockage; Partial Blockage
IT WAS REPORTED BY THE CUSTOMER THAT THEY WERE HAVING A PROBLEM WITH LIQUID NOT GOING THROUGH. CUSTOMER REPORTED HAVING A HARD TIME FLUSHING THE IV ONCE IT'S INSERTED AND FLUIDS ARE FLOWING VERY SLOWLY. 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 23758364 ↗MalfunctionAug 20, 2025Fail-Safe Problem; Fail-Safe Problem
IT WAS REPORTED BY THE CUSTOMER THAT THE NEEDLE DOES NOT RETRACT & EXTEND COMPLETELY AS IT SHOULD. 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 22854163 ↗MalfunctionAug 14, 2025Fail-Safe Problem; Fail-Safe Problem
IT WAS REPORTED BY THE CUSTOMER THAT PUSH BUTTON IS NOT RETRACTING THE NEEDLE AND WHEN HELD UPSIDE DOWN THE NEEDLE FALLS OUT. 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 22803793 ↗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 22591538 ↗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 22202665 ↗MalfunctionMay 29, 2025Fail-Safe Problem; Fail-Safe Problem
IT WAS REPORTED BY THE CUSTOMER THAT THE NEEDLE WILL HANG OUT OF THE CHAMBER AFTER BEING INJECTED INTO THE VEIN ONCE IT HAS BEEN RETRACTED. 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 22106518 ↗
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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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