BD Difco™ Salmonella O Antiserum Group C1 Factors 6, 7 229491Recalls & reported problems
Becton, Dickinson And Company · BD Difco™ Salmonella O Antiserum Group C1 Factors 6, 7, 3 mL · Class 2
Data updated Oct 18, 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 00382902294917), received between May 29, 2026 and May 29, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “False Positive Result” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- False Positive Result1
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.
MalfunctionMay 29, 2026False Positive Result
IT WAS REPORTED WHILE USING THE BD DIFCO¿ SALMONELLA O ANTISERUM GROUP C1 FACTORS 6, 7, A PATIENT SAMPLE WAS IDENTIFIED BY THE REFERENCE LABORATORY AS GROUP R POSITIVE RATHER THAN C1 POSITIVE. NO PATIENT IMPACT OR CONSEQUENCE REPORTED. THIS IS REPORT 2 OF 2.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25336881 ↗
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 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 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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