ClearanceBrief
Recall Z-1620-2021 ยท QKP Coronavirus Antigen Detection Test System.

LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD

Leccurate SARS-CoV-2, Antigen Rapid Test Kit (Colloidal Gold Immunochromatography), 1 test, IVD. for the qualitative detection of antigen SARS-CoV-2 in clinical samples (nasal swab).

DateApr 26, 2021
StatusCompleted
ReasonAntigen Rapid Test Kit is not authorized, cleared, or approved for marketing and/or distribution in the U.S.
Root causeNo Marketing Application
ActionOn 4/26/2021, Lepu Medical issued an "Urgent: Medical Device Recall Notification" to all affected consignees. In addition, to informing consignees about the recall, Lepu asked consignees to take the following actions: (1) Quarantine and discontinue distribution of All Lots of the abovementioned products which were distributed to U.S. (2) Please complete the acknowledgement form and send to recall@lepu-medical.com within 5 business days. If you no longer have any of the recalled product, please also complete the acknowledgement form and return to us by email above. (3) If your firm has distr
Quantity8, 419, 545 units in total
DistributionWorldwide Distribution: US Distribution to states of: FL, IL, NY, GA, Puerto Rico and OUS countries of: Canada, Honduras, Peru, Dominican, Bolivia, Colombia, Mexico, Brazil, Argentina, Guatemala, Venezuela, Ecuador, Chile, Paraguay, Panama, Costa Rica, Peru and Hong Kong.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.