BD Vacutainer® Sodium HeparinN Blood Collection Tubes 368037Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30382903680376), received between Jul 10, 2023 and Jul 10, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Product Quality Problem” (1 report).

2 other recalls cover devices cleared under the same FDA submission (K944566); they may or may not involve this specific model.

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

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 10, 2023Product Quality Problem; Product Quality Problem

  IT WAS REPORTED THAT WHILE USING BD VACUTAINER® SODIUM HEPARINN BLOOD COLLECTION TUBES THAT THERE WAS INSUFFICIENT ADDITIVES. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: CUSTOMER STATES TUBES ARRIVED WITHOUT SODIUM HEPARIN ADDITIVE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17286923 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K944566. One submission often covers many models, so check the product and lot details in each record.

• Z-2307-2019 · Jun 12, 2019 · Terminated
  BD Vacutainer PST Gel and Lithium HeparinN (LH) 56 Units Blood Collection Tubes, Catalog Number 368056
• Z-2306-2019 · Jun 12, 2019 · Terminated
  BD Vacutainer PST Blood Collection Tubes, Catalog Number 368035, 368036