BD BACTEC Lytic/10 Anaerobic/F Culture VialsRecalls & reported problems across all models
Becton, Dickinson And Company · 2 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 804
- Deaths reported
- 1
- Injuries reported
- 15
- Recalls
- 0
We found 2 models of BD BACTEC Lytic/10 Anaerobic/F Culture Vials by Becton, Dickinson And Company in the FDA's device registry (GUDID). Together they are named in 804 adverse event reports in the FDA's MAUDE database, received between Feb 4, 2021 and Sep 30, 2026 — classified as 1 death, 15 injuries, 788 malfunctions.
The most frequently reported specific device problem is “False Positive Result” (603 reports).
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
Reports received per month, all models
Most reported BD BACTEC Lytic/10 Anaerobic/F Culture Vials problems
Device problems
- False Positive Result603
- Incorrect, Inadequate or Imprecise Result or Readings106
- False Negative Result42
- Contamination32
- Leak/Splash15
- Contamination of Device Ingredient or Reagent7
- Device Markings/Labelling Problem5
- Fluid/Blood Leak2
Patient problems
- No Clinical Signs, Symptoms or Conditions795
- Insufficient Information7
- No Consequences Or Impact To Patient2
- Bacterial Infection1
- No Information1
- Sepsis1
BD BACTEC Lytic/10 Anaerobic/F Culture Vials models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- BD BACTEC™ Lytic/10 Anaerobic/F Culture Vials 442021SYSTEM, BLOOD CULTURING1 death791 reports
- BD BACTEC™ Lytic/10 Anaerobic/F Culture Vials 442265SYSTEM, BLOOD CULTURING13 reports
Recent BD BACTEC Lytic/10 Anaerobic/F Culture Vials adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026False Negative Result
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950614 ↗MalfunctionSep 30, 2026False Negative Result
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50950608 ↗MalfunctionSep 30, 2026False Negative Result
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50947256 ↗MalfunctionSep 30, 2026False Negative Result
It was reported that while using BD BACTEC¿ Lytic/10 Anaerobic/F Culture Vials (plastic), an unspecified number of false-negative results were obtained. No adverse impact was reported regarding the patient or user.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50947252 ↗MalfunctionSep 30, 2026False Negative Result
It was reported that while using BD BACTEC¿ Lytic/10 Anaerobic/F Culture Vials (plastic), an unspecified number of false-negative results were obtained. No adverse impact was reported regarding the patient or user.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50947251 ↗MalfunctionSep 30, 2026False Negative Result
It was reported that while using BD BACTEC¿ Lytic/10 Anaerobic/F Culture Vials (plastic), an unspecified number of false-negative results were obtained. No adverse impact was reported regarding the patient or user.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50947249 ↗MalfunctionSep 30, 2026False Negative Result
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50947246 ↗MalfunctionSep 30, 2026False Negative Result
It was reported that while using BD BACTEC¿ Lytic/10 Anaerobic/F Culture Vials (plastic), an unspecified number of false-negative results were obtained. No adverse impact was reported regarding the patient or user.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50947244 ↗MalfunctionSep 30, 2026False Negative Result
It was reported that while using BD BACTEC¿ Lytic/10 Anaerobic/F Culture Vials (plastic), an unspecified number of false-negative results were obtained. No adverse impact was reported regarding the patient or user.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50947243 ↗MalfunctionSep 30, 2026False Negative Result
It was reported that while using BD BACTEC¿ Lytic/10 Anaerobic/F Culture Vials (plastic), an unspecified number of false-negative results were obtained. No adverse impact was reported regarding the patient or user.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50947241 ↗MalfunctionSep 30, 2026False Negative Result
It was reported that while using BD BACTEC¿ Lytic/10 Anaerobic/F Culture Vials (plastic), an unspecified number of false-negative results were obtained. No adverse impact was reported regarding the patient or user.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50947220 ↗MalfunctionSep 29, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50938139 ↗MalfunctionSep 29, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50938128 ↗MalfunctionAug 18, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50302060 ↗MalfunctionAug 14, 2026Incorrect, Inadequate or Imprecise Result or Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50253457 ↗
Other Becton, Dickinson And Company products
- BD Vacutainer SST10 models · 4,985 reports · 3 recalls
- BD Luer-Lok48 models · 5,117 reports
- BD Insyte Autoguard33 models · 4,465 reports · 8 recalls
- BD SafetyGlide17 models · 2,185 reports
- BD Vacutainer Eclipse Blood Collection Needle4 models · 1,880 reports
- BD Vacutainer Push Button Blood Collection Set9 models · 1,831 reports
- BD Nexiva25 models · 1,614 reports · 1 recall
- BD BACTEC MGIT Mycobacteria Growth Indicator Tubes2 models · 1,554 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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