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Phadia US Inc recalls Phadia 1000 Instrument, Article Number 12-3800-01.
Recalled January 24, 2018 · FDA recall Z-0387-2018 · Phadia US
Hazard
The "Retry" command does not function properly which could cause a shortage of Wash and Rinse solution and affect assay performance and test results. · FDA Class II
Units
70 units
Sold at
Nationwide
Description
The "Retry" command does not function properly which could cause a shortage of Wash and Rinse solution and affect assay performance and test results.
Product
Phadia 1000 Instrument, Article Number 12-3800-01.
Manufacturer(s)
Phadia US Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →