Medical device recalls

Abbott Laboratories recalls ARCHITECT STAT High Sensitive Troponin-I Controls - Product Usage: The ARCHITECT STAT High Sensitive Troponin-I Control…

Recall date
April 9, 2019
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1359-2019
FDA classification
Class III
Brand / firm
Abbott Laboratories
Sold / distributed
Distribution to Latvia.

Why it was recalled

Devices were delivered without the required dry ice.

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

ARCHITECT STAT High Sensitive Troponin-I Controls - Product Usage: The ARCHITECT STAT High Sensitive Troponin-I Controls are for the estimation of test precision and the detection of systematic analytical deviations of the ARCHITECT i System with STAT protocol capability when used for the quantitative determination of cardiac troponin I (cTnI) in human serum and plasma with the ARCHITECT STAT High Sensitive Troponin-I reagent kit.

Get recall alerts

Free email alert whenever Abbott Laboratories has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Abbott Laboratories