Inova Diagnostics QUANTA-Lyser 240 EIA, Part #GS0241 recall — FDA Z-1222-2018
The device power supply was not manufactured according to specification which can result in the loss of the protective grounding of the instrument.
Overview of recall records associated with Inova Diagnostics Inc., including dates, categories and classifications where available.
Classification mix: Class II: 2.
The device power supply was not manufactured according to specification which can result in the loss of the protective grounding of the instrument.
The device power supply was not manufactured according to specification which can result in the loss of the protective grounding of the instrument.
This page summarizes recall records in which the official source identifies Inova Diagnostics Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.