Medical device recalls Moderate risk

Mckesson Medical-Surgical Inc. Corporate Office recalls ABBOTT DIAGNOSTICS ARCHITECT PROGESTERONE (100TESTS) REAGENT.

Recall date
April 24, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1851-2025
FDA classification
Class II
Brand / firm
Mckesson Medical-Surgical Inc. Corporate Office
Sold / distributed
US Nationwide distribution in the states of AL, AR, IL, KS, MT, NC, NJ, OR, SC, TN & WV.

Why it was recalled

transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.

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

What was recalled

ABBOTT DIAGNOSTICS ARCHITECT PROGESTERONE (100TESTS) REAGENT.

Get recall alerts

Free email alert whenever Mckesson Medical-Surgical Inc. Corporate Office has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Mckesson Medical-Surgical Inc. Corporate Office