safety hypodermic needles 25G×25mmRWRecalls & reported problems
Berpu Medical Technology Co.,Ltd · 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 06949236204001), received between Feb 18, 2022 and Feb 18, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Too Soft/Flexible” (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.
Most reported problems
Device problems
- Material Too Soft/Flexible1
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.
MalfunctionFeb 18, 2022Material Too Soft/Flexible; Material Too Soft/Flexible
ON (B)(6) 2022, A USER FACILITY REPORTED A COMPLAINT WITH THE BERPU SAFETY NEEDLES, 25G X 1 INCH, THAT WERE SUPPLIED IN THE COVID VACCINE ANCILLARY CONVENIENCE KITS. REPORTER INDICATED THAT THE SAFETY NEEDLES ARE VERY FLIMSY. BOTH THE NEEDLE AND THE SAFETY LATCH BEND EASILY, WHICH LED TO A NEEDLESTICK INJURY ON (B)(6) 2022 AT ONE OF THEIR PRIMARY CARE LOCATIONS.
Patient problems: Needle Stick/Puncture
MAUDE report 13562211 ↗
Other Needle, Hypodermic, Single Lumen devices
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- N/A 305110Becton, Dickinson And Company · Needle, hypodermic, single lumen418 reports
- BD Safe-Clip 328235Becton, Dickinson and Company Inc · Needle, hypodermic, single lumen268 reports
- BD Ultra-Fine 320109Becton Dickinson Pen Limited · Needle, hypodermic, single lumen229 reports
- BD AutoShield Duo 329515Becton, Dickinson And Company · Needle, hypodermic, single lumen208 reports
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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