BD Perisafe, BD Epilor, BD Luer-Lok 406048Recalls & reported problems
Becton, Dickinson And Company · TRAY EPID CONT WE18G3.5 C20 LOR5 B DRAP · Class 2
All models of BD Perisafe, BD Epilor, BD Luer-Lok (9)
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 50382904060485), received between Jan 22, 2020 and Jan 22, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Complete Blockage” (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
- Complete Blockage1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 22, 2020Complete Blockage; Complete Blockage
IT WAS REPORTED THAT TRAY EPID CONT WE18G3.5 C20 LOR5 B DRAP WOULD NOT ALLOW FLUID TO FLOW THROUGH IT. THIS WAS DISCOVERED DURING USE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: MATERIAL NO.: 406048 BATCH NO.: 0001262389 IT WAS REPORTED THAT FLUID WOULD NOT FLOW THROUGH THE EPIDURAL CATHETER. PER PHONE CALL ON (B)(6) 2019: HEALTH PROFESSIONAL REPORTED THAT FLUID WOULD NOT COME OUT OF THE CATHETER AS IF THERE WAS NO HOLE AT THE END OF IT. THEY HAD TO SHORT DELAY THE PROCEDURE TO GET A NEW CATHETER FROM A TRAY AND RESTICK THE PATIENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9616450 ↗
Other Anesthesia conduction kit devices
- BD Luer-Lok, BD Glaspak 405671Becton, Dickinson And Company · Anesthesia conduction kit1 recall68 reports
- 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 Glaspak 405675Becton, 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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