Search results
Results from the WOW.Com Content Network
Costco announced a recall of Kirkland Severe Cold & Flu Capsules due to the potential of foreign material contamination. ... Cold & Flu Plus Congestion capsules were sold between October 30, 2024 ...
The recall said the packages bear item number 1729556 and would have been purchased between October 30, 2024 and November 30, 2024. The lot code printed on the back of the affected boxes is P140082 .
Phenylpropanolamine was previously available in the United States over-the-counter and in certain combination drug forms by prescription. [24] [25] One such example of the latter was a combination of phenylpropanolamine and chlorpheniramine, which dually contained decongestant and antihistamine effects, marketed by Tutag as 'Vernate'.
The vomer (/ ˈ v oʊ m ər /; [1] [2] Latin: vomer, lit. 'ploughshare') is one of the unpaired facial bones of the skull . It is located in the midsagittal line, and articulates with the sphenoid , the ethmoid , the left and right palatine bones, and the left and right maxillary bones.
Misuse of multisymptom cold medications, rather than use of a cough suppressant whose sole active ingredient is dextromethorphan, carries significant risk of fatality or serious illness. Multisymptom cold medicines contain other active ingredients, such as paracetamol (acetaminophen), which can cause permanent bodily damage such as kidney ...
A major recall of nearly 12 million pounds of meat and poultry that may have been contaminated with listeria has affected stores nationwide Costco recalls more items over listeria fears. What we ...
FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.
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]