Shifeng N-2510Recalls & reported problems
Chengdu Xinjin Shifeng Medical Apparatus & Instrument Co., Ltd. · Class 2
Data updated Oct 16, 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 G001N25100), received between Nov 11, 2022 and Nov 11, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Physical Resistance/Sticking” (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 16, 2026.
Most reported problems
Device problems
- Physical Resistance/Sticking1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 11, 2022Physical Resistance/Sticking; Physical Resistance/Sticking
CUSTOMER REPORTED THAT THE ISSUE WAS WITH THE SHIFENG PRODUCT SUPPLIED IN THE KIT, INDICATING THAT THE SAFETY DOESN'T ALWAYS LATCH RIGHT AWAY. IT TAKES MORE PRESSURE TO GET THE SAFETY TO ENGAGE. CUSTOMER PROVIDED MFR# N-2510 AND LOT # 210307 AS ADDITIONAL PRODUCT IDENTIFICATION INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15781234 ↗
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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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