BD BBL™ Selective 7H11 Agar Slants 297639Recalls & reported problems
Becton, Dickinson And Company · BD BBL™ Selective Seven H11 Agar Ctn. of 100 slants (size A tubes) · Class 1
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 30382902976395), received between Jun 18, 2026 and Jun 18, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Contamination /Decontamination Problem” (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
- Contamination /Decontamination Problem1
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 18, 2026Contamination /Decontamination Problem
IT WAS REPORTED, SYRINGE 10ML SALINE FILL CHINA SP, FOREIGN MATTER. THE FOLLOWING WAS PROVIDED BY THE INITIAL REPORTER: BEFORE INFUSION, THE PATIENT PLANNED TO PERFORM A FLUSHING TUBE BUT FOUND AN ABNORMALITY AT THE PREFILLING CONNECTOR, A WHITE PLASTIC SUBSTANCE BLOCKING THE CONNECTOR, SO IT WAS IMMEDIATELY NOT USED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25548235 ↗
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- BD BBL™ XLD Agar 221284Becton, Dickinson And Company · CULTURE MEDIA, SELECTIVE AND NON-DIFFERENTIAL9 reports
- BD BBL™ Lowenstein-Jensen Medium, Gruft, Slants 297653Becton, Dickinson And Company · CULTURE MEDIA, SELECTIVE AND NON-DIFFERENTIAL5 reports
- BD BBL™ Middlebrook and Cohn 7H10 Agar Slants 220958Becton, Dickinson And Company · CULTURE MEDIA, SELECTIVE AND NON-DIFFERENTIAL2 reports
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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