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The recalled medicine is Kirkland Signature brand's "Severe Cold and Flu Plus Congestion" medication, sold between Oct. 30 and Nov. 30, 2024. The recalled items have a Lot Code of P140082 on the box.
The product affected is the Kirkland Signature Severe Cold & Flu Plus Congestion tablets. The impacted packages have a printed lot code of P140082 and were sold between October 30, 2024, and ...
According to the announcement, the capsules were recalled when a batch of the medicine was accidentally released and shipped after being "rejected" due to potential foreign material contamination ...
Pholcodine is not prescribed in the United States where it is classed as a Schedule I drug, the most highly controlled drug category. [4] Following the conclusion of a review of post-marketing safety data by the MHRA, all pholcodine-containing medicines are being recalled and withdrawn from the UK as a precaution. [5]
Withdrawn from US in 2005 due to hepatotoxicity. [41] [3] Pentobarbital: 1980 Norway Risk of fatal overdose. [3] Pentylenetetrazol: 1982 US Withdrawn for inability to produce effective convulsive therapy, and for causing seizures. Pergolide (Permax) 2007 US Risk for heart valve damage. [2] Perhexiline: 1985 UK, Spain Neurologic and hepatic ...
A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug recall. [1]
The boxes of caplets, which include both day and night medications, are being pulled "due to potential foreign material contamination," according to a Jan. 2 notice Costco shared on its website ...
Pholcodine can trigger allergic reactions and is common in cough syrups