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Phadia Ab recalls Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is fully integrated and automated instrument includin
Recalled September 4, 2019 · FDA recall Z-2397-2019 · Phadia Ab
Hazard
code 7-102 Liquid Sensor Error · FDA Class II
Units
387 Instruments
Sold at
US Nationwide Distribution in the states of CA CO FL GA HI IL IN KS KY MA MD MI MO NC NJ NV NY OH OK OR PA TN TX UT VA WA
Description
code 7-102 Liquid Sensor Error
Product
Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is fully integrated and automated instrument including software for immunodiagnostic testing. The instrument is designed to handle all steps from sample and reagent handling to processing of results.
Manufacturer(s)
Phadia Ab
Made in
Sweden
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →