BD Glaspak 405675Recalls & reported problems
Becton, Dickinson And Company · TRAY SPN WHIT25G3.5 25G1.5 L/B-D/E · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 50382904056754), received between Aug 7, 2018 and Jun 24, 2022 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Manufacturing, Packaging or Shipping Problem” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
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. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Apr 27, 2026Open, Classified
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.
Z-2255-2026 · Root cause: Nonconforming Material/Component · FDA record ↗
Most reported problems
Device problems
- Manufacturing, Packaging or Shipping Problem1
- Patient-Device Incompatibility1
- Volume Accuracy Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 24, 2022Patient-Device Incompatibility; Patient-Device Incompatibility
IT WAS REPORTED THAT THE BD GLASPAK SPINAL ANESTHESIA TRAY FAILED TO WORK. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: WE HAVE A SPECIFIC LOT OF BD SPINAL TRAYS WHERE THE DRUGS IN THE TRAY DID NOT WORK AS INTENDED FOR THE ANESTHESIOLOGIST.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14799649 ↗MalfunctionJul 30, 2021Volume Accuracy Problem; Volume Accuracy Problem
IT WAS REPORTED TRAY SPN WHIT25G3.5 25G1.5 L/B-D/E WAS LABELED INCORRECTLY, WITH FILL MARKINGS INCORRECTLY PLACED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "HASH MARKS ON 5ML SYRINGE IN EPIDURAL KIT DO NOT LINE UP WITH THE HUB/BASE OF THE SYRINGE. THIS COULD HAVE RESULTED IN DELIVERING APPROX 1ML ADDITIONAL MEDICATION THAN INTENDED. ANESTHESIOLOGIST, DR , NOTED ISSUE UPON DRAWING UP MEDICATION AND HANDED OFF MIS-MARKED SYRINGE IMMEDIATELY. NEW KIT OPENED--SAME MANUF NUMBER, SAME LOT NUMBER BUT THE SYRINGE WITHIN WAS CORRECT."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12256194 ↗MalfunctionAug 7, 2018Manufacturing, Packaging or Shipping Problem
IT WAS REPORTED THAT THE PACKAGED BD WHITACRE SPINAL TRAYS HAD DIFFERENT ITEMS IN THE TRAYS AND WERE MISSING TWO DRUGS. THERE WAS NO REPORT OF EXPOSURE, INJURY, OR MEDICAL INTERVENTION NOTED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7759834 ↗
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 405609Becton, Dickinson And Company · Anesthesia conduction kit1 recall3 reports
- BD Luer-Lok, BD Glaspak 405735Becton, 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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