BD Durasafe Plus, BD Epilor 400286Recalls & reported problems
Becton, Dickinson And Company · DURASAFE+EL CSE M-KIT 27G WHX17G WS PLOR · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00382904002862), received between Mar 2, 2018 and Mar 2, 2018 — classified as 1 injury.
The most frequently reported specific device problem is “Device Or Device Fragments Location Unknown” (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
- Device Or Device Fragments Location Unknown1
Patient problems
- Device Embedded In Tissue or Plaque1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 2, 2018Device Or Device Fragments Location Unknown
IT WAS REPORTED THAT DURING RETRACTION OF A BD DURASAFE PLUS¿ EPIDURAL LOCK CSE NEEDLE SET, THE DISTAL PART OF THE CATHETER REMAINED IN THE TISSUES OF THE PATIENT. IT WAS NOT POSSIBLE TO VERIFY THE EXACT POSITIONING OF THE PART AND NO FURTHER CONSEQUENCES WERE REPORTED BECAUSE THEY DID NOT IDENTIFY ANY PART OF THE CATHETER IN THE PATIENT'S BODY.
Patient problems: Device Embedded In Tissue or Plaque
MAUDE report 7310298 ↗
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- ARROW IPN922678Teleflex Incorporated · Anesthesia conduction kit2 recalls0 reports
- BD Luer-Lok, BD Glaspak 405672Becton, Dickinson And Company · Anesthesia conduction kit1 recall27 reports
- BD Luer-Lok, BD Glaspak 405673Becton, Dickinson And Company · Anesthesia conduction kit1 recall10 reports
- BD Luer-Lok, BD Glaspak 405637Becton, Dickinson And Company · Anesthesia conduction kit1 recall7 reports
- BD Luer-Lok, BD Glaspak 405707Becton, Dickinson And Company · Anesthesia conduction kit1 recall4 reports
- BD Luer-Lok, BD Glaspak 405735Becton, Dickinson And Company · Anesthesia conduction kit1 recall3 reports
- BD Luer-Lok, BD Glaspak 405609Becton, Dickinson And Company · Anesthesia conduction kit1 recall3 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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