Biomerieux Recalls
431 recalls on record · October 17, 2012 to July 15, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
Also filed under
The recall feeds record what looks like the same company under more than one name:
November 28, 2012Medical DevicesFDA
Biomerieux Inc recalls bioMerieux Kit, Instrument & Update, 3D B.40 ZIP-ML06, Clinical instrument software, Japanese, Korean, Norwegian, Brazi
Hazard: The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
November 28, 2012Medical DevicesFDA
Biomerieux Inc recalls bioMerieux Kit, Instrument & Update, 3D B.40 ZIP-ML05, Clinical instrument software, Lithuanian, Latvian, Russian, Slov
Hazard: The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
November 28, 2012Medical DevicesFDA
Biomerieux Inc recalls bioMerieux Kit, Instrument & Update, 3D B.40 ZIP-ML04, Clinical instrument software, Czech, Estonian, Hungarian, Romani
Hazard: The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
November 28, 2012Medical DevicesFDA
Biomerieux Inc recalls bioMerieux Kit, Instrument & Update, 3D B.40 ZIP-ML03, Clinical instrument software, Danish, Greek, Polish, Portuguese,
Hazard: The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
November 28, 2012Medical DevicesFDA
Biomerieux Inc recalls bioMerieux Kit, Instrument & Update, 3D B.40 BTA3D-ZH01, Clinical instrument software, Chinese, catalog number 411816
Hazard: The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
November 28, 2012Medical DevicesFDA
Biomerieux Inc recalls bioMerieux Kit, Instrument & Update, 3D B.40 ZIP-ML 02, Clinical instrument software, English, Spanish, Italian, catalo
Hazard: The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
November 28, 2012Medical DevicesFDA
Biomerieux Inc recalls bioMerieux Kit, Instrument & Update, 3D B.40 ZIP-ML01, Clinical instrument software, English, Spanish, Italian, catalog
Hazard: The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
November 28, 2012Medical DevicesFDA
Biomerieux Inc recalls bioMerieux BacT/ALERT 3D 60, catalog number, 248009, Clinical instrument The product is most commonly used to isolate
Hazard: The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
November 28, 2012Medical DevicesFDA
Biomerieux Inc recalls bioMerieux BacT/ALERT Combo Module, catalog number, 200290, Clinical instrument The product is most commonly used to
Hazard: The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
November 28, 2012Medical DevicesFDA
Biomerieux Inc recalls bioMerieux BacT/ALERT Control Module, catalog number 210147, Clinical instrument The product is most commonly used to
Hazard: The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
October 17, 2012Medical DevicesFDA
Biomerieux Inc recalls PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculati
Hazard: The instrument may not dispense the specimen onto the pre-poured media resulting in a false negative result.