McKesson 192-PB2475WRecalls & reported problems
Mckesson Medical-Surgical Inc. · Catheter, IV safety, push button, sterile, Yellow, Winged 24G x .75 in · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10612479250212), received between Aug 12, 2024 and Oct 2, 2024 — classified as 2 injuries, 2 malfunctions.
The most frequently reported specific device problem is “Retraction Problem” (2 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
- Retraction Problem2
- Fluid/Blood Leak1
- Physical Resistance/Sticking1
Patient problems
- Needle Stick/Puncture2
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryOct 2, 2024Retraction Problem; Retraction Problem
IT WAS REPORTED THAT BD INSYTE AUTOGUARD NEEDLE PARTIALLY RETRACTED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: JUST WANTED TO CHECK WITH YOU ON A SITUATION. I HAD A MA THAT WAS GIVING A PATIENT AN IV. THE NEEDLE DIDN'T RETRACT ALL THE WAY IN AND SHE STUCK HERSELF WHILE TRYING TO CLEAN UP. THE PATIENT IS HIV POSITIVE AND ALSO HAS HEPATITIS C. I DID ALL THE THINGS NECESSARY FOR THE PATIENT BUT THE OWNER WANTED ME TO REACH OUT WITH THE LOT NUMBER AND FOR YOU TO CHECK AND SEE IF THE MANUFACTURER HAS A KNOWN ISSUE WITH THIS. MCKESSON BRAND 24 G X 0.75 IN SHIELDED IV CATHETER LOT # 3096297 AND EXP DATE IS 3/31/26. THE MA WENT TO THE ER AND WAS GIVEN PRESCRIPTION PROPHYLACTICS TO TAKE FOR 4 WEEKS WITH FOLLOW UPS AT INTERVALS.
Patient problems: Needle Stick/Puncture
MAUDE report 20355802 ↗InjuryOct 1, 2024Retraction Problem; Retraction Problem
MalfunctionAug 13, 2024Physical Resistance/Sticking; Physical Resistance/Sticking
IT WAS REPORTED THAT BD INSYTE AUTOGUARD WING SAFETY DEVICE WAS DIFFICULT TO ACTIVATE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THE SAFETY RELEASE BUTTON FOR NEEDLE IS VERY HARD TO PUSH, & AND WHEN REMOVING NEEDLE IT IS CAUSING BLEEDING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19974417 ↗MalfunctionAug 12, 2024Fluid/Blood Leak; Fluid/Blood Leak
NO ADDITIONAL INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19965789 ↗
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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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