McKesson 192-PB221WRecalls & reported problems
Mckesson Medical-Surgical Inc. · Catheter, IV safety, push button, sterile, Blue, Winged 22G x 1 in · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10612479250182), received between Jul 28, 2021 and May 7, 2022 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Fail-Safe Did Not Operate” (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.
Most reported problems
Device problems
- Fail-Safe Did Not Operate1
- Retraction 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.
InjuryMay 7, 2022Fail-Safe Did Not Operate; Fail-Safe Did Not Operate
IT WAS REPORTED THAT MCKESSON IV SAFETY BLUE WING 22GA X1.0IN HAD A NEEDLE RETRACTION FAILURE THAT RESULTED IN A DIRTY NEEDLE STICK. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: ''NURSE JUST COMPLETED DRAWING BLOOD - PUT THE NEEDLE ON A TRAY - WENT TO PICK UP THE NEEDLE - THE NEEDLE WAS NOT RETRACTED AND GOT STUCK BY THE NEEDLE.¿
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14319606 ↗MalfunctionJul 28, 2021Retraction Problem; Retraction Problem
IT WAS REPORTED THAT MCKESSON IV SAFETY BLUE WING 22GA X1.0IN HAD A RETRACTION FAILURE. THIS OCCURRED ON 2 OCCASIONS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS REPORTED THAT 2 IV CATHETERS DID NOT RETRACT WHEN BUTTON WAS PUSHED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12240034 ↗
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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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