Strep Selective II Agar R01859Recalls & reported problems
Remel, Inc. · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- Jul 11, 2025Class IIOpen, Classified
The products may contain surface and subsurface contamination of Listeria monocytogenes.
Z-2224-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Other Culture Media, Selective And Differential devices
- REMEL R02041Remel, Inc. · Culture Media, Selective And Differential3 recalls0 reports
- BD BBL™ MacConkey II Agar 221270Becton, Dickinson And Company · CULTURE MEDIA, SELECTIVE AND DIFFERENTIAL1 recall64 reports
- CHROMID® Candida AgarBiomerieux SA · CULTURE MEDIA, SELECTIVE AND DIFFERENTIAL1 recall28 reports
- CHROMID® C. difficileBiomerieux SA · CULTURE MEDIA, SELECTIVE AND DIFFERENTIAL1 recall3 reports
- REMEL R02049Remel, Inc. · Culture Media, Selective And Differential1 recall0 reports
- BD BBL™ CHROMagar™ Candida 254093Becton, Dickinson And Company · CULTURE MEDIA, SELECTIVE AND DIFFERENTIAL29 reports
- CHROMID® S. aureus Elite agarBiomerieux SA · CULTURE MEDIA, SELECTIVE AND DIFFERENTIAL9 reports
- BD BBL™ Hektoen Enteric Agar 221365Becton, Dickinson And Company · CULTURE MEDIA, SELECTIVE AND DIFFERENTIAL6 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
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- 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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