BD Difco™ Salmonella O Antiserum Group E Factors 1, 3, 10, 15, 19, 34 228191Recalls & reported problems
Becton, Dickinson And Company · BD Difco™ Salmonella O Antiserum Group E Factors 1, 3, 10, 15, 19, 34, 3 mL · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00382902281917), received between Oct 17, 2023 and Jun 21, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Incorrect, Inadequate or Imprecise Result or Readings” (2 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, 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.
Reports received per month
Most reported problems
Device problems
- Incorrect, Inadequate or Imprecise Result or Readings2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 21, 2024Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED WHILE USING THE BD DIFCO¿ SALMONELLA O ANTISERUM GROUP E FACTORS 1, 3, 10, 15, 19, 34 A WEAK AGGLUTINATION REACTION OCCURRED. NO HEALTH IMPACT OR CONSEQUENCE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19587014 ↗MalfunctionOct 17, 2023Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
IT WAS REPORTED THAT WHILE USING BD DIFCO¿ SALMONELLA O ANTISERUM GROUP E FACTORS 1, 3, 10, 15, 19, 34, THERE WAS A PERFORMANCE ISSUE OF ONE VIAL. THE PERFORMANCE ISSUE IS UNABLE TO BE LISTED AS INSUFFICIENT INFORMATION WAS PROVIDED. NO PATIENT IMPACT REPORTED. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "CAN'T BE TESTED."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17953655 ↗
Other ANTISERA, ALL GROUPS, SALMONELLA SPP. devices
- NA R30957301Remel Europe Limited · Antisera, All Groups, Salmonella Spp.1 recall0 reports
- BD Difco™ Salmonella O Antiserum Factor 7 228161Becton, Dickinson And Company · ANTISERA, ALL GROUPS, SALMONELLA SPP.4 reports
- BD Difco™ Salmonella H Antiserum Single Factor 2 224741Becton, Dickinson And Company · ANTISERA, ALL GROUPS, SALMONELLA SPP.2 reports
- BD Difco™ Salmonella H Antiserum Single Factor 5 224751Becton, Dickinson And Company · ANTISERA, ALL GROUPS, SALMONELLA SPP.2 reports
- BD Difco™ Salmonella O Antiserum Group C1 Factors 6, 7 229491Becton, Dickinson And Company · ANTISERA, ALL GROUPS, SALMONELLA SPP.1 report
- BD Difco™ Salmonella O Antiserum Group A Factors 1, 2, 12 229471Becton, Dickinson And Company · ANTISERA, ALL GROUPS, SALMONELLA SPP.1 report
- BD Difco™ Salmonella H Antiserum Single Factor t 225511Becton, Dickinson And Company · ANTISERA, ALL GROUPS, SALMONELLA SPP.1 report
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 14, 2026 · each report above links to its original FDA record
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page