Devices

Device Recall PREVI Isola System

Model / Serial
Serial numbers AS180-00001 to AS180-00376.
Product Classification
Clinical Chemistry and Clinical Toxicology Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide Distribution-USA (nationwide)-including DC and the states of CA, CO, CT, FL, GA, IL, IN, KY, LA, MO, NC, NJ, NY, OH, OR, PA, RI, SC, TX, and WI, and the country of Canada.
Product Description
PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. || Intended to perform the inoculation and streaking of Prepoured Media (PPM) with liquid microbiological samples.
Manufacturer
Biomerieux Inc
1 Event
- Recall of Device Recall PREVI Isola System

Manufacturer

Biomerieux Inc

Manufacturer Address
Biomerieux Inc, 595 Anglum Rd, Hazelwood MO 63042-2320
Manufacturer Parent Company (2017)
Compagnie Merieux Alliance
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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