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BD BBL™ Lim Broth 296266Recalls & reported problems

Becton, Dickinson And Company · BD BBL™ Lim Broth, 5 mL, Carton of 100 size K tubes · Class 1

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30382902962664), received between Jun 17, 2022 and Jun 17, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Leak/Splash” (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 16, 2026.

Most reported problems

Device problems

  • Leak/Splash1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionJun 17, 2022Leak/Splash; Leak/Splash

    IT WAS REPORTED THAT BD BBL¿ LIM BROTH TWO TUBES BROKE IN EMPLOYEE'S HANDS WHEN OPENING. NO PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: LIM BROTH TUBES 296266 - 2 TUBES BROKE IN (EMPLOYEE) HANDS WHEN OPENING.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14739446 ↗

Other CULTURE MEDIA, SELECTIVE BROTH devices

All CULTURE MEDIA, SELECTIVE BROTH devices →

Sources and updates

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