RELI® SBCN-R22G101Recalls & reported problems
Myco Medical Supplies Inc. · RELI® Safety Blood Collection Needle 22G x 1”, Sterile · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10386120009350), received between Jul 10, 2024 and Jul 10, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
- Fitting Problem1
- Improper or Incorrect Procedure or Method1
- Lack of Effect1
- Leak/Splash1
Patient problems
- Needle Stick/Puncture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 10, 2024Break; Leak/Splash; Improper or Incorrect Procedure or Method; Fitting Problem; Lack of Effect; Break; Leak/Splash; Improper or Incorrect Procedure or Method; Fitting Problem; Lack of Effect
8 TEAMMATES COMMENTS THAT THE "TUBES POP" OFF AND WHEN REAPPLYING TUBES ARE NOT FILLING PROPERLY. 4 TEAMMATES COMMENTS THAT THE DEVICE IS DIFFICULT TO SCREW ONTO THE ADAPTERS THAT IT CROSS THREADS. 3 TEAMMATES THAT THEY HAVE HAD THE SAFETY FEATURECOMPLETELY BREAK OFF WHEN APPLYING ONTO THE HUB·MULTIPLE TEAM HAVE SAID THE NEEDLES ONCE SET UP THEY HAVE HAD DIFFICULTYREMOVING THE CAP TO EXPOSE THE COLLECTION NEEDLE ·2 HAVE HAD THE RUBBER THAT CLOSES OFF THE BLOOD FROM ENTERING THE TUBECOME OFF OR PARTIALLY COME OFF DURING COLLECTION RESULTING IN BLOOD SPILLAGE. " DEVICE SEEMS MORE BULKIER, AND CUMBERSOMEBECAUSE THE SAFETY SHIELD GETS IN THE WAY AND WHEN REPOSITIONED THE SAFETY FEATURE BECOMES WEAKENED AND HAS BROKEN " "HAVE HAD SOME THAT THE SAFETY GUARD WERE ALREADY DISLODGED PRIOR TO SET UP" "SAFETY DEVICE HAD NOT CLOSED PROPERLY SEVERALTIMES, CONCERNED ABOUT GETTING ACCIDENTLY STUCK"·"SAFETY SHIED DOES NOT OPEN FULLY TO VIEW COLLECTION SITE PRECISELY"·WE RECENTLY HAD A LONG-TIME EMPLOYEE HAVE AN ACCIDENTAL DIRTY NEEDLE STICK DUE TO SAFETY SHIELD WOULD NOT OPEN FULLY FOR VIEW.
Patient problems: Needle Stick/Puncture
MAUDE report 19709360 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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