REMEL R01202Recalls & reported problems
Remel, Inc. · Blood Agar,5% Sheep Blood 100/PK · Class 1
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
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. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Jul 11, 2025Open, Classified
The products may contain surface and subsurface contamination of Listeria monocytogenes.
Z-2223-2025 · Root cause: Under Investigation by firm · FDA record ↗
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- BD BBL™ Rapid Urea Broth 298330Becton, Dickinson And Company · CULTURE MEDIA, NON-SELECTIVE AND DIFFERENTIAL2 reports
- BD BBL™ Urease Test Broth 221719Becton, Dickinson And Company · CULTURE MEDIA, NON-SELECTIVE AND DIFFERENTIAL1 report
- BD BBL™ Simmons Citrate Agar Slants 221026Becton, Dickinson And Company · CULTURE MEDIA, NON-SELECTIVE AND DIFFERENTIAL1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.