McKesson 16-SNALL1C27Recalls & reported problems
Mckesson Medical-Surgical Inc. · Allergist Tray, 1cc · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 20612479207275), received between May 8, 2024 and May 8, 2024 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Dull, Blunt” (4 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
- Dull, Blunt4
- Leak/Splash2
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- Insufficient Information1
- Limb Pain1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 8, 2024Dull, Blunt; Dull, Blunt
IT WAS REPORTED BY THE CUSTOMER THAT THE NEEDLES ARE TOO BLUNT AND ARE CAUSING PAIN AND SWELLING.IN ADDITION, WHEN THE STAFF DRAWS UP THE SERUM, IT PUSHES THE SERUM OUT WITHOUT PRESSING THE PLUNGER RESULTING IN LEAKAGE OF MEDICATION.NO INFORMATION WAS RECEIVED REGARDING ANY SERIOUS INJURY AS A RESULT OF THESE REPORTED ISSUES.
Patient problems: Limb Pain
MAUDE report 19266481 ↗MalfunctionMay 8, 2024Leak/Splash; Dull, Blunt; Leak/Splash; Dull, Blunt
IT WAS REPORTED BY THE CUSTOMER THAT FOR LOWER DOSES, THE SYRINGES WITHIN THE ALLERGIST TRAY ARE CAUSING THE MEDICATION TO SPIT OUT BEFORE ADMINISTRATING ALL OF IT INTO THE PATIENT'S ARM.IT WAS ALSO REPORTED THAT THE NEEDLE IS DIFFICULT TO PENETRATE THE SKIN, RESULTING PAINFUL SHOTS.NO INFORMATION WAS RECEIVED REGARDING ANY SERIOUS INJURY AS A RESULT OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19266467 ↗MalfunctionMay 8, 2024Dull, Blunt; Dull, Blunt
THE NEEDLES WERE VERY DULL AND CAUSING PATIENT REACTION.
Patient problems: Insufficient Information
MAUDE report 19266463 ↗MalfunctionMay 8, 2024Leak/Splash; Leak/Splash
IT WAS REPORTED BY THE CUSTOMER THAT THE MEDICATION DOES NOT COME OUT OF THE NEEDLE BUT RATHER COMES OUT OF THE SIDES OF THE PLUNGER. NO INFORMATION WAS RECEIVED REGARDING ANY SERIOUS INJURY AS A RESULT OF THIS REPORT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19266433 ↗MalfunctionMay 8, 2024Dull, Blunt; Dull, Blunt
THREE NEEDLE WOULD NOT EVEN GO INTO THE SKIN OF A PATIENT. HAD TO THROW AWAY SECONDARY TO STERILITY. MANY OTHERS THE TOPS DO NOT COME OFF.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19266381 ↗
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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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