Medical device recalls Moderate risk

Codan US Corporation recalls CODAN SWAN-LOCK Swabable Needlefree Connector, Catalog #BC1000N, REF 16.7220, individually packaged, 504/case, Sterile.…

Recall date
September 12, 2019
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2433-2020
FDA classification
Class II
Brand / firm
Codan US Corporation
Sold / distributed
Distribution was made to CA, MI, NY, PA, and VA. There was no military/government distribution. Foreign distribution was made to Canada, Australia, New Zealand, and Chile.

Why it was recalled

Individual packages of connectors may have incomplete or bad seals which would compromise sterility.

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

What was recalled

CODAN SWAN-LOCK Swabable Needlefree Connector, Catalog #BC1000N, REF 16.7220, individually packaged, 504/case, Sterile. The firm name on the label is CODAN US CORPORATION, Santa Ana, CA.

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