DrugDec 18, 2024
SEVERE COLD AND FLU PLUS CONGESTION Kirkland Severe Cold & Flu Plus Congestion: Day - 112 recall — FDA D-0115-2025
CGMP Deviations: Released product should have been rejected.
Class IIFDA: TerminatedLNK International, Inc.
Recall history in this database
Classification mix: Class III: 3, Class II: 2.
DrugOct 26, 2022
SINUS PRESSURE, PAIN AND COUGH NDC 0363-6171-09 Walgreens Sinus Pressure, Pain & Cough recall — FDA D-0014-2023
Boxes mislabeled to read "Decongestant Free", but the product contains Phenylephrine HCI 5mg
Class IIIFDA: TerminatedLNK International, Inc.
DrugSep 7, 2022
LNK International Nighttime Sleep-Aid (doxylamine succinate HCl) tablets, 25 mg, 48-count recall — FDA D-1472-2022
Labeling: Not Elsewhere Classified: Carton incorrectly identifies product as doxylamine succinate HCl, however the product is doxylamine succinate.
Class IIIFDA: TerminatedLNK International, Inc.
DrugJul 28, 2021
LNK International Acetaminophen EXTRA STRENGTH Pain Reliever / Fever Reducer, Enteric recall — FDA D-0665-2021
Labeling: Not Elsewhere Classified The primary label contains the words "enteric coated" but the tablet is not enteric coated and should only say 'coated tablet'
Class IIIFDA: TerminatedLNK International, Inc.
DrugDec 31, 2014
LNK International Walgreens ASPIRIN FREE TENSION HEADACHE, Pain Reliever/Pain Reliever Aid recall — FDA D-0319-2015
Incorrect/Undeclared Excipients: The firm recalled specific lots of Walgreens brand Aspirin Free Tension Headache Caplets due to the presence of sucralose, which was not declared on the…
Class IIFDA: TerminatedLNK International, Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies LNK International, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.