RecallRadar

FDA Device recall Z-1594-2023

Pilot COVID-19 At-Home Test, Reference Number 9901-NCOV-10G, Catalog Number 99COV200L-EN02, UPC Code: 887473000207 (EAN-13: 08800111707728)

On 2023-05-31 the FDA classified a Class I recall of Pilot COVID-19 At-Home Test, Reference Number 9901-NCOV-10G, Catalog Number 99COV200L-EN02, UPC Code: 887473000207 (EAN-13: 08800111707728) by Sd Biosensor, citing the liquid buffer component in the affected test kit lots was determined to have bacterial contamination. User may notice a slight odor when the buffer is brought close to the nose.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1594-2023
ClassificationClass I
Statusongoing
Initiated2023-03-31
Published2023-05-31
Last updated2026-09-13 11:56 UTC
CompanySd Biosensor
DistributionUS

Product

Pilot COVID-19 At-Home Test, Reference Number 9901-NCOV-10G, Catalog Number 99COV200L-EN02, UPC Code: 887473000207 (EAN-13: 08800111707728)

Reason

The liquid buffer component in the affected test kit lots was determined to have bacterial contamination. User may notice a slight odor when the buffer is brought close to the nose.

Identifiers

upc887473000207
code_info
Lot Numbers: 53K41T5T1 53K41X1T1 53K41X2T1 53K41X3T1 53K4211T1 53K4212T1 53K4213T1 53K4221T1 53K4222T1 53K4223T1 53K422…Lot Numbers: 53K41T5T1 53K41X1T1 53K41X2T1 53K41X3T1 53K4211T1 53K4212T1 53K4213T1 53K4221T1 53K4222T1 53K4223T1 53K4224T1 53K4225T1 53K4231T1 53K4232T1 53K4233T1 53K4261T1 53K4262T1 53K4271T1 53K4272T1 53K4273T1 53K4274T1 53K4291T1 53K4292T1 53K42A1T1 53K42A2T1 53K42A3T1 53K42E1T1 53K42G1T1 53K42G2T1 53K42H1T1 53K42H2T1 53K42L1T1 53K42L2T1 53K4361AC 53K4362AC 53K4392AC 53K38N3T1 53K38N2T1 53K38N1T1 53K38N4T1 53K38N5T1 53K38P1T1 53K38P2T1 53K38P3T1

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1594-2023%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.