BD Luer-Lok, BD Glaspak 405651Recalls & reported problems
Becton, Dickinson And Company · Tray SPN WHIT24G3.5 L/B-D/E · Class 2
All models of BD Luer-Lok, BD Glaspak (16)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 50382904056518), received between May 2, 2018 and May 2, 2018 — classified as 2 injuries.
The most frequently reported specific device problem is “Device Inoperable” (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
- Device Inoperable1
- Device Operates Differently Than Expected1
Patient problems
- No Code Available1
- Pain1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 2, 2018Device Operates Differently Than Expected
IT WAS REPORTED WHILE PERFORMING A PROCEDURE WITH A BD¿ WHITACRE SPINAL TRAY WITH THE USE OF LIDOCAINE AS THE ANESTHESIA MEDICATION, THE MEDICATION WAS FOUND TO BE INEFFECTIVE. AS A RESULT, WHEN THE PATIENT WAS PINCH TESTED AT THE INCISION SITE, THE PATIENT "STARTED BUCKING." THE PATIENT WAS PLACED UNDER GENERAL ANESTHESIA FOR THE REMAINDER OF THE PROCEDURE.
Patient problems: No Code Available
MAUDE report 7480428 ↗InjuryMay 2, 2018Device Inoperable
IT WAS REPORTED WHILE PERFORMING A PROCEDURE WITH A BD¿ WHITACRE SPINAL TRAY WITH THE USE OF LIDOCAINE AS THE ANESTHESIA MEDICATION, THE MEDICATION WAS FOUND TO BE INEFFECTIVE. AS A RESULT, WHEN THE PATIENT WAS PINCH TESTED AT THE INCISION SITE, THE PATIENT "STARTED BUCKING." THE PATIENT WAS PLACED UNDER GENERAL ANESTHESIA FOR THE REMAINDER OF THE PROCEDURE.
Patient problems: Pain
MAUDE report 7480421 ↗
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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