BD Perisafe, BD Epilor, BD Luer-Lok 406069Recalls & reported problems
Becton, Dickinson And Company · TRAY EPID SST18G3.5 S/L · 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
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 50382904060690), received between Mar 10, 2021 and May 21, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Device Markings/Labelling Problem” (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
- Device Markings/Labelling Problem1
- Tear, Rip or Hole in Device Packaging1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 21, 2025Tear, Rip or Hole in Device Packaging; Tear, Rip or Hole in Device Packaging
MATERIAL # 406069, BATCH # UNKNOWN. IT WAS REPORTED BY CUSTOMER THAT HOLES OR TEARS IN DRAPE WHEN OPENING THE STERILE TRAY VERBATIM: HOLES OR TEARS IN DRAPE WHEN OPENING THE STERILE TRAY. THIS HAS OCCURRED WITH A FEW DIFFERENT TRAYS. THE DRAPES WERE USED, BUT NO PT INJURY OR ADVERSE EVENT. 1. CAN YOU PLEASE PROVIDE AN EXACT DATE OF EVENT IN THIS FORMAT MM-DD-YYYY? 05-08-2025. 2. CAN YOU PLEASE PROVIDE THE LOT NUMBER ASSOCIATED WITH REPORTED ISSUE? UNFORTUNATELY, WE ARE NOT CERTAIN THIS MAY HAVE BEEN THE SAME LOT # AS THE TRAYS WITH DRAPE HOLES/TEARS. WE RECEIVE SEVERAL CASES EVERY OTHER DAY. LOT #0001611311.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22059928 ↗MalfunctionMar 10, 2021Device Markings/Labelling Problem; Device Markings/Labelling Problem
IT WAS REPORTED THAT THE TRAY EPID SST18G3.5 S/L CAME WITH A METAL-TIPPED GLASS SYRINGE INSTEAD OF THE CORRECT GLASS-TIPPED SYRINGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "IT IS SUPPOSED TO HAVE A GLASS SYRINGE WITH A GLASS TIP AS NOTED ON THE PACKAGE. THE TRAY IS COMING WITH A GLASS SYRINGE WITH A METAL TIP AND PER THE PHYSICIAN ¿ CANNOT BE USED FOR THESE PROCEDURES. (HUGE SAFETY ISSUE)"
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11458176 ↗
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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