McKesson 200-IVRW221Recalls & 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
- 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 10612479268583), received between Oct 20, 2025 and Jun 11, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Difficult or Delayed Activation” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Difficult or Delayed Activation1
- Fail-Safe Did Not Operate1
- Fail-Safe Problem1
- Fluid/Blood Leak1
- Improper or Incorrect Procedure or Method1
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.
MalfunctionJun 11, 2026Improper or Incorrect Procedure or Method; Difficult or Delayed Activation; Fail-Safe Did Not Operate
CUSTOMER PROVIDED THE FOLLOWING DESCRIPTION: NEEDLE DOESN'T RETRACT WHEN BUTTON IS PUSHED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25477789 ↗MalfunctionApr 22, 2026Fluid/Blood Leak
CUSTOMER REPORTED THE ITEM WAS LEAKING AT THE CONNECTION. THIS COULD BE INDICATIVE OF THERE BEING A PUNCTURE THROUGH THE CATHETER WHICH COULD POTENTIALLY LEAD TO SHEARING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24958198 ↗MalfunctionOct 20, 2025Fail-Safe Problem; Fail-Safe Problem
IT WAS REPORTED BY THE CUSTOMER THAT SOME OF THE NEEDLES DO NOT RETRACT COMPLETELY. 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 23335579 ↗
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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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