Kirkland Severe Cold & Flu Plus Congestion: Day - 112 recall: CGMP Deviations
Kirkland Severe Cold & Flu Plus Congestion: Day - 112 coated caplets blister pack; (Acetaminophen 325mg, Dextromethorphan HBr 10 mg, Guaifenesin 200…
Why was Kirkland Severe Cold & Flu Plus Congestion: Day - 112 recalled?
CGMP Deviations: Released product should have been rejected.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot # P139953, exp. date 2026/AUG Lot # P139815, exp. date 2026/AUG
- Product
- Kirkland Severe Cold & Flu Plus Congestion: Day - 112 coated caplets blister pack; (Acetaminophen 325mg, Dextromethorphan HBr 10 mg, Guaifenesin 200…
- Recalling firm
- LNK International, Inc.
- Quantity
- 288 cases x 30 8,640 boxes
- Distribution
- Product was distributed to 1 wholesale retail customer who may have further distribute the product nationwide.
- Recall date
- December 18, 2024
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)