Medical device recalls Moderate risk

Quidel Corporation recalls Influenza Transport Swab Packages, Reference #20171, One lot with 1010 packages (each package contains 25 transport tub…

Recall date
January 25, 2017
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1231-2017
FDA classification
Class II
Brand / firm
Quidel Corporation
Sold / distributed
Nationwide Distribution to FL, GA, IL, IN, KY, MT, OH, PA, TX

Why it was recalled

Quidel Corporation is recalling Influenza Transport Swab Packages because it may include an incorrect sample swab mixed in with the proper swabs.

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

What was recalled

Influenza Transport Swab Packages, Reference #20171, One lot with 1010 packages (each package contains 25 transport tubes). The Influenza Swabs in dry transport tubes are intended for use with influenza tests

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