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Device Recall ABL 800 FLEX analyzers
Model / Serial
ABL 800 FLEX series blood gas analyzers containing software version 5.24.
Product Classification
Clinical Chemistry and Clinical Toxicology Devices
Device Class
2
Implanted device?
No
Distribution
The recalled analyzers were distributed to customers nationwide throughout the U.S. and in some parts of Canada.
Product Description
ABL 800 FLEX series blood gas analyzers containing software version 5.24.
Manufacturer
Radiometer America Inc
1 Event
Recall of Device Recall ABL 800 FLEX analyzers
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Manufacturer
Radiometer America Inc
Manufacturer Address
Radiometer America Inc, 810 Sharon Dr, Westlake OH 44145-1598
Source
USFDA
Language
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