BD GlaspakRecalls & reported problems across all models

We found 2 models of BD Glaspak by Becton, Dickinson And Company in the FDA's device registry (GUDID). Together they are named in 4 adverse event reports in the FDA's MAUDE database, received between Aug 7, 2018 and Jun 24, 2022 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Manufacturing, Packaging or Shipping Problem” (2 reports).

2 FDA recall records name at least one of these models by its device identifier, 2 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

BD Glaspak recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. Apr 27, 2026Class IOpen, 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 · Recall details · FDA record ↗

2. Apr 27, 2026Class IOpen, 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-2250-2026 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗

Most reported BD Glaspak problems

BD Glaspak models

2 models, most reported first. Each model has its own page with its reports, recalls and device details.

• BD Glaspak 405675

  Anesthesia conduction kit
  1 recall3 reports
• BD Glaspak 405632

  Anesthesia conduction kit
  1 recall1 report

Recent BD Glaspak adverse event reports

The 4 most recent reports across all models, 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 ↗
• MalfunctionMar 15, 2019Manufacturing, Packaging or Shipping Problem

  IT WAS REPORTED THAT THE TRAY SPN QNKE26G3.5 L/B-D WAS NOTICED TO HAVE INCORRECT CONTENT WITHIN IT BEFORE USE, AS IT DID NOT CONTAIN "BUPIVACAINE". AS REPORTED BY THE CUSTOMER, "PER CUSTOMER, REPORTED THE PACK HAD THE WRONG CONTENTS IN THE PACK. THE PACK THEY RECEIVED DID NOT CONTAIN BUPIVACAINE."

  Patient problems: No Information

  MAUDE report 8425372 ↗
• 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 ↗

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