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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of a review of post-marketing safety data by the MHRA, all pholcodine-containing medicines are being recalled and withdrawn from the UK as a precaution.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]
Pholcodine can trigger allergic reactions and is common in cough syrups
For questions about this recall, call 1-800-426-9391 or email complaints-inquiries@lnkintl.com. Related: Cheese Is Being Recalled Due to Possible Listeria Contamination—Here’s What to Know ...
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.
Drugs or medicines may be withdrawn from commercial markets because of risks to patients, but also because of commercial reasons (e.g. lack of demand and relatively high production costs).
This is the list of Schedule I controlled substances in the United States as defined by the Controlled Substances Act. [1] The following findings are required for substances to be placed in this schedule: [2]
Brimonidine Tartrate Ophthalmic Solution, 0.15%: A special tool designated for those with glaucoma or ocular hypertension, a small subset of these eye drops are being voluntarily recalled as ...
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]
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