Yeso med 25G×1'' (0.5×25)Recalls & reported problems
Wuxi Yushou Medical Appliances CO.,Ltd. · Safety hypodermic needle without syringe · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 06971352289020), received between Jan 11, 2022 and Dec 8, 2023 — classified as 1 injury, 4 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Retraction Problem2
- Unintended Movement2
- Detachment of Device or Device Component1
- Dull, Blunt1
- Material Protrusion/Extrusion1
- Material Twisted/Bent1
- Output Problem1
Patient problems
- Needle Stick/Puncture4
- Insufficient Information1
- Pain1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
InjuryDec 8, 2023
DIRTY NEEDLE STICK. RN HAD JUST FINISHED AN IM(INTRAMUSCULAR) VACCINE INJECTION AND WAS ACTIVATING THE SAFETY ON THE NEEDLE. THE NEEDLE DID NOT SLIDE INTO THE SAFETY AND INSTEAD CURLED UP POKING THE PALM OF THE RN'S HAND.
Patient problems: Needle Stick/Puncture
MAUDE report 18302760 ↗MalfunctionAug 3, 2023Retraction Problem; Unintended Movement; Retraction Problem; Unintended Movement
COMPLAINANT REPORTED MULTIPLE NEEDLESTICK EVENTS WHERE THE SAFETY SHIELDS ON THE ORANGE 25GX1" NEEDLE COMPLETELY FALLS OFF.
Patient problems: Needle Stick/Puncture
MAUDE report 17455206 ↗MalfunctionAug 3, 2023Retraction Problem; Unintended Movement; Retraction Problem; Unintended Movement
COMPLAINANT REPORTED MULTIPLE NEEDLESTICK EVENTS WHERE THE SAFETY SHIELDS ON THE ORANGE 25GX1" NEEDLE COMPLETELY FALLS OFF.
Patient problems: Needle Stick/Puncture
MAUDE report 17455205 ↗OtherMay 11, 2023Material Protrusion/Extrusion; Material Twisted/Bent
THE NEEDLE IS VERY FLIMSY. IT BENDS WHEN TRYING TO PENETRATE A MEDICATION VIAL, I HAVE ALSO SEEN IT BEND WHEN TRYING TO GIVE AN INJECTION (ON A HUMAN). AND NOW TODAY, THE NEEDLE WAS SO FLIMSY IT BENT WHEN TRYING TO ACTIVATE THE SAFETY CAP OVER THE NEEDLE. SO ONLY A SMALL PORTION OF THE NEEDLE IS IN THE SAFETY CAP AND A LARGER PORTION OF THE SHARP NEEDLE IS PROTRUDING OUTSIDE OF THE EDGES OF THE SAFETY CAP. (B)(6). SUBMISSION ID: (B)(4).
Patient problems: Insufficient Information
MAUDE report 16919582 ↗MalfunctionFeb 23, 2023Dull, Blunt; Dull, Blunt
THE NURSE WHO ADMINISTERED THE COVID-19 VACCINE REPORTED THAT SHE FACED ISSUES WHILE USING THE 25G, 1" DPS SAFETY NEEDLE. THE NEEDLE POINT WAS NOT SHARP; IT WAS BLUNT. THE COMMON ISSUE OCCURRED WHEN VACCINATING A PATIENT. THE NEEDLE PENETRATION REQUIRED EXTRA FORCE, AND FEEDBACK WAS RECEIVED FROM THE PATIENT THAT THE EXPERIENCE WAS PAINFUL.
Patient problems: Pain
MAUDE report 16431846 ↗MalfunctionJan 11, 2022Detachment of Device or Device Component; Output Problem
PFIZER USE FOR COVID-19 UNDER EMERGENCY USE AUTHORIZATION (EUA): WHILE BEING VACCINATED, THE NEEDLE STAYED IN THE PATIENT'S ARM ONCE THE SYRINGE WAS PULLED AWAY. THIS EQUIPMENT MALFUNCTION RESULTED IN A NURSE BEING POKED BY THE CONTAMINATED NEEDLE. FDA SAFETY REPORT ID# (B)(4).
Patient problems: Needle Stick/Puncture
MAUDE report 13236138 ↗
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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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