BD Difco™ Salmonella H Antiserum Single Factor 2 224741Recalls & reported problems
Becton, Dickinson And Company · BD Difco™ Salmonella H Antiserum Single Factor 2, 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 00382902247418), received between Jul 28, 2025 and Jul 28, 2025 — 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.
MalfunctionJul 28, 2025Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
REPORT 2 OF 2: IT WAS REPORTED WHILE USING BD DIFCO¿ SALMONELLA H ANTISERUM SINGLE FACTOR 2, THERE WAS A FALSE POSITIVE AGGLUTINATION REACTION FOR MONOPHASIC STRAINS OF SALMONELLA TYPHIMURIUM. NO PATIENT IMPACT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22634164 ↗MalfunctionJul 28, 2025Incorrect, Inadequate or Imprecise Result or Readings; Incorrect, Inadequate or Imprecise Result or Readings
REPORT 1 OF 2. IT WAS REPORTED WHILE USING BD DIFCO¿ SALMONELLA H ANTISERUM SINGLE FACTOR 2, THERE WAS A FALSE POSITIVE AGGLUTINATION REACTION FOR MONOPHASIC STRAINS OF SALMONELLA TYPHIMURIUM. NO PATIENT IMPACT REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22627901 ↗
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 O Antiserum Group E Factors 1, 3, 10, 15, 19, 34 228191Becton, 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.
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