Quantimetrix Dropper Plus Point-of-Care Urinalysis Dipstick Control kit The Quantimetrix recall — FDA Z-2257-2018
The kits contained an incorrect lot of Dropper Plus Level 1 vials
Overview of recall records associated with Quantimetrix Corporation, including dates, categories and classifications where available.
Classification mix: Class III: 1.
The kits contained an incorrect lot of Dropper Plus Level 1 vials
This page summarizes recall records in which the official source identifies Quantimetrix Corporation 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.