BD Cathena™ Safety IV Catheter 386882Recalls & reported problems
Becton, Dickinson And Company · US CATHENA 22GX2.00IN WINGED BC · Class 2
All models of BD Cathena Safety IV Catheter (33)
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 00382903868827), received between Jan 30, 2025 and Jan 30, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Protrusion/Extrusion” (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
- Material Protrusion/Extrusion1
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 30, 2025Material Protrusion/Extrusion; Material Protrusion/Extrusion
IT WAS REPORTED THAT BD US CATHENA 22GX2.00IN WINGED BC SAFETY MECHANISM FAILED. IT WAS REPORTED BY CUSTOMER THAT THE NEEDLE SAFETY FEATURE FAILED, AND NEEDLE TIP IS EXPOSED UPON REMOVAL. ALSO STATED THAT THE WINGS ARE NOT STURDY. VERBATIM: NEEDLE SAFETY FEATURE FAILED; NEEDLE TIP EXPOSED UPON REMOVAL. NONE, NO INJURY. DISCARDED NEEDLE INSHARPS CONTAINER. THIS WAS A 22 GAUGE 2¿ CATHENA AND INSERTED WITH ULTRASOUND. CLINICIAN STATED THE WINGS ARE NOT STURDY AND WOULD PREFER THE DEVICE WITHOUT WINGS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21277443 ↗
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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