Medical device recalls Moderate risk

CELLTRION USA INC recalls Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02

Recall date
February 25, 2022
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0731-2022
FDA classification
Class II
Brand / firm
CELLTRION USA INC
Sold / distributed
The products were distributed to the following US states: CA, CT, FL, HI, MA, MT, NJ, NY, PA, TN, and TX.

Why it was recalled

Kits were labeled with incorrect expiration dates.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02

Get recall alerts

Free email alert whenever CELLTRION USA INC has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: CELLTRION USA INC