RELI® SBCN-R21G114Recalls & reported problems
Myco Medical Supplies Inc. · RELI® Safety Blood Collection Needle 21G x 1.25”, 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 10386120009336), received between Sep 5, 2024 and Sep 5, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Dull, Blunt” (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
- Dull, Blunt1
- Fail-Safe Did Not Operate1
- Fluid/Blood Leak1
Patient problems
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 5, 2024Fluid/Blood Leak; Dull, Blunt; Fail-Safe Did Not Operate; Fluid/Blood Leak; Dull, Blunt; Fail-Safe Did Not Operate
1. THE PUNCTURE END OF NEEDLE POINT WILL CAUSE ADDITIONAL PAIN WHEN INSERTED; 2. THE SEPARATION FORCE BETWEEN THE PROTECTIVE CAP AND THE NEEDLE HUB IS LARGE, WHICH IS DIFFICULT TO PULL OUT, AND THERE IS A RISK OF PRICK DURING OPERATION; 3. A PHLEBOTOMIST THINKS THAT THE NEEDLE POINT IS BLUNT AND THE PRODUCT IS FRAGILE; 4. VACUUM BLOOD COLLECTION TUBE IS EASY TO FALL OFF WHEN IT IS CONNECTED WITH OUR PRODUCT, AND IT IS DIFFICULT TO INSERT THE VACUUM BLOOD COLLECTION TUBE AGAIN AFTER FALLING OFF. POSSIBLE CAUSES: (1) THE PRODUCT DOES NOT MATCH THE VACUUM BLOOD COLLECTION TUBE, WHICH IS THE PROBLEM OF THE VACUUM BLOOD COLLECTION TUBE; (2) THE RUBBER SLEEVE FOR SAFETY BLOOD-COLLECTING NEEDLE IS TOO THICK. 5. IT IS DIFFICULT TO TWIST THE SAFETY BLOOD-COLLECTING NEEDLE WHEN IT IS CONNECTED WITH THE NEEDLE HOLDER, AND IT TAKES MORE TIME TO OPERATE; 6. THE SAFETY MECHANISM IS COMPLETELY DISCONNECTED DURING APPLICATION; 7. DURING BLOOD COLLECTING, WHEN THE PUNCTURE END OF NEEDLE POINT IS INSERTED IN THE ARM, THE SAFETY MECHANISM WILL MOVE FORWARD AND BLOCK THE SIGHT, WHICH WILL AFFECT THE BLOOD COLLECTING OPERATION; 8. DURING BLOOD COLLECTION, THE RUBBER SLEEVE FALLS OFF OR FALLS OFF PARTIA
Patient problems: Pain
MAUDE report 20153893 ↗
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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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