BD Luer-Lok 405727Recalls & reported problems
Becton, Dickinson And Company · TRAY SPN WHIT27G3.5 · Class 2
All models of BD Luer-Lok (48)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 50382904057270), received between Jun 19, 2018 and Jun 4, 2021 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (2 reports).
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 Contamination with Chemical or Other Material2
- Microbial Contamination of Device1
- Packaging Problem1
Patient problems
- No Known Impact Or Consequence To Patient3
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 4, 2021Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material
IT WAS REPORTED THAT TRAY SPN WHIT27G3.5 HAD FOREIGN MATTER. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS REPORTED FOREIGN MATERIAL. CUSTOMER STATES THEY HAVE FOUND PARTICLES IN THEIR ANESTHESIA TRAYS. ANESTHESIOLOGIST THREW THE TRAY TO THE SIDE IN DISGUST.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 11943538 ↗MalfunctionFeb 26, 2020Packaging Problem; Packaging Problem
IT WAS REPORTED THAT TRAY SPN WHIT27G3.5 HAD COMPROMISED STERILITY. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "STERILE WRAPPING STUCK ON OUTER PACKAGING."
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9753798 ↗MalfunctionOct 16, 2018Microbial Contamination of Device
IT WAS REPORTED THAT THE BD¿ REGIONAL ANESTHESIA TRAYS SPN WHIT27G3.5 WERE "CONTAMINATED". THERE WAS NO REPORT OF EXPOSURE, INJURY, OR MEDICAL INTERVENTION.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7970874 ↗MalfunctionJun 19, 2018Device Contamination with Chemical or Other Material
IT WAS REPORTED WITH THE USE OF THE BD REGIONAL ANESTHESIA TRAY SPN (B)(4) THERE WAS AN ISSUE WITH FOREIGN MATTER. IT WAS STATED ¿FOREIGN MATTER IS COVERING THE SYRINGE AND THE PACKAGING OF THE PRODUCT.¿ THERE WAS NO REPORT OF INJURY OR FURTHER MEDICAL INTERVENTION.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7613866 ↗
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 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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