BD Angiocath 382277Recalls & reported problems
Becton, Dickinson And Company · ANGIOCATH SPECIAL LGT BL 12GA X 3.0IN · Class 2
All models of BD Angiocath (8)
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 00382903822775), received between Jan 9, 2023 and Jan 9, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Separation” (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 Separation1
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.
MalfunctionJan 9, 2023Material Separation; Material Separation
IT WAS REPORTED WHILE USING BD ANGIOCATH¿ IV CATHETER THE CATHETER SEPARATED FROM THE HUB. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS STATED BY THE CUSTOMER THAT IT WAS DISCOVERED THAT THE ELONGATED SHEATH CAN BE DISCONNECTED FROM THE HUB COMPONENT OF THE SHEATH. THE HUB COMPONENT WAS UNKNOWINGLY LEFT INSITU WHILST CANNULATION OCCURRED. THIS RESULTED IN A PARTIAL CANNULATION TO ENABLE ATTACHMENT OF A BUNG AT THE CATHETER END. A FULLY ADVANCED CATHETER WOULD COVER THE HUB AND THE CANNULA COULDN¿T BE ACCESSED TO BE CAPPED OFF, RESULTING IN BLEED BACK.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16127938 ↗
Other Catheter,intravascular,therapeutic,short-term less than 30 days devices
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- BD Insyte Autoguard Shielded IV Catheter 381823Becton, Dickinson And Company · Catheter, intravascular, therapeutic, short-term less than 30 days582 reports
- BD Insyte Autoguard 381423Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days1 recall528 reports
- BD Insyte Autoguard 382544Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days1 recall437 reports
- BD Nexiva, BD Q-Syte 383536Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days2 recalls374 reports
- BD PosiFlush 306547Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days2 recalls1 death331 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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