Medical DeviceJun 16, 2021
INNOVA MEDICAL GROUP COVID-19 Self-Test Kit *** INNOVA *** 3T recall — FDA Z-1539-2021
Due to distributing test kits to customers who were not part of a clinical investigation.
Class IFDA: OngoingINNOVA MEDICAL GROUP, Inc.
Recall history in this database
Classification mix: Class I: 3.
Medical DeviceJun 16, 2021
INNOVA MEDICAL GROUP For In Vitro Diagnostic Use Only *** 25T 888 SARS-CoV-2 Antigen *** recall — FDA Z-1538-2021
Due to distributing test kits to customers who were not part of a clinical investigation.
Class IFDA: OngoingINNOVA MEDICAL GROUP, Inc.
Medical DeviceJun 16, 2021
INNOVA MEDICAL GROUP COVID-19 Self-Test Kit *** INNOVA *** 7T recall — FDA Z-1537-2021
Due to distributing test kits to customers who were not part of a clinical investigation.
Class IFDA: OngoingINNOVA MEDICAL GROUP, Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies INNOVA MEDICAL GROUP, 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.