FDASeptember 17, 2019drug

Lidocaine Hydroclhoride Jelly USP, 2%, 30 mL tubes, Rx Only, Sterile, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC 17478-711-30

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

cGMP Deviations: firm reported finding metal particulate matter in the filling room near the tube feeder during the filling operation of the product. No particulates were identified in the product, but rather were identified on the filling line.

What to do

FDA enforcement status: Terminated

Brands named

akorn

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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