Recall Z-1537-2021

Innova Medical Group, Inc. · initiated April 9, 2021

Class I Open, Classified

Class I – dangerous or defective products that could cause serious health problems or death

Product

COVID-19 Self-Test Kit *** INNOVA *** 7T

Codes / lots: Catalog Number: 7T Lot Numbers: U2101748 U2102001 U2102002 X2012711 X2103792

Reason for recall

Due to distributing test kits to customers who were not part of a clinical investigation.

FDA-determined cause: No Marketing Application

Action taken

On or about 04/26/2021, the firm sent an "URGENT: MEDICAL DEVICE RECALL" Notification via email to its customers informing them that it is recalling products that were distributed outside of a clinical investigation and that the affected products are for investigational use only. The performance characteristics have not been establish and the tests should not be used to screen or diagnose COVID-19. The negative results obtained on the tests are not indicator of the status of SARS-CoV-2 infection. Customers are instructed to: -Check their inventory to see if they have in their possession the affected products. -If they have affected products, they are to count the test kits and write the number on the accompanying "MEDICAL DEVICE RECALL RETURN RESPONSE" form and return the form to the Recalling Firm via the provided FedEx envelope. -Destroy (by placing in your household waste) or return the affected products (Customer's choice), but to include the total number of destroyed and returned test on the "MEDICAL DEVICE RECALL RETURN RESPONSE" form. For any questions or assistance, contact Linda Weinreb at Linda.Weinreb@innovamedgroup.com or 747-494-0852.

Details

Recall number
Z-1537-2021
Initiated
April 9, 2021
Product code
QKP – Coronavirus Antigen Detection Test System.
Quantity
370 boxes (=2,590 individual tests)
Distribution
Worldwide distribution - U.S. Nationwide in the states of AL, AZ, CA, CO, CT, DC, DE, FL, GA, IL, IN, KY, MA, MD, ME, MI, MN, MO, NC, NE, NH, NJ, NV, NY, OH, PA, RI, TN, TX, UT, VA, VT, WA, and WI. The countries of Canada, India and United Kingdom.
Recalling firm
Innova Medical Group, Inc., Pasadena, CA

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-1538-2021 Class IFor In Vitro Diagnostic Use Only *** 25T 888 SARS-CoV-2 Antigen *** SARS-CoV-2 Antigen…Due to distributing test kits to customers who were not part of a clinical investigation. 04/09/2021Open, Classified
Z-1539-2021 Class ICOVID-19 Self-Test Kit *** INNOVA *** 3TDue to distributing test kits to customers who were not part of a clinical investigation. 04/09/2021Open, Classified