Public Alert No: 29/2021 – Prairie Wolf Spirits Inc. Recalls Prairie Wolf Distillery Hand Sanitizer Packed In 16.9 Oz And 20.0 Oz Bottles Resembling Drinking Water Containers
, The National Agency for Food and Drug Administration and Control (NAFDAC) has received information from US FDA on the voluntary recall by manufacturer of Prairie Wolf Distillery hand sanitizer packaged in 16.9 fluid ounce (UPC 6000331899) and 20.0 fluid ounce (UPC 6000365984) containers to the consumer level. The product poses a risk of ingestion […]
Public Alert No. 28/2021 – Alert on Recall of Chantix (Varenicline) Tablets by Pfizer, Due to the Presence of Nitrosamine, N-Nitroso-Varenicline above Pfizer Established Acceptable Daily Intake (ADI) Level.
, The National Agency for Food and Drug Administration and Control (NAFDAC) has received information from US FDA that Pfizer is voluntarily recalling twelve (12) lots of Chantix (Verencline) Tablets – two 0.5 mg tablet lots, two 1.0 mg tablet lots, and eight lots of a Chantix kit that includes both 0.5 mg and 1.0 […]
