Jacobus Pharmaceutical Company Inc. Issues Voluntary Worldwide Recall of Ruzurgi® (Amifampridine) 10 mg Tablets Due to Yeast, Mold, and Bacterial Contamination
, Dear Healthcare Provider, The National Agency for Food and Drug Administration and Control (NAFDAC) has been informed by U.S Food and drug Administration (FDA) that Jacobus Pharmaceutical Company Inc. is voluntarily recalling 3 lots of Ruzurgi® (Amifampridine) 10 mg tablets to the consumer level. The products were found to be contaminated with yeast, mold, and […]
Baxter Issues Urgent Medical Device Correction for All Spectrum IQ Infusion Pumps to Reinforce Important Safety Information Regarding Best Practices for Customer-Initiated IT Network Updates
, The National Agency for Food and Drug Administration and Control (NAFDAC) has been informed by U.S Food and drug administration (FDA) about a safety communication that Baxter International Inc. has issued an Urgent Medical Device Correction for all Spectrum IQ infusion pumps to reinforce important safety information when customers implement changes to their network […]
Public Alert No: 036/2021 – Recall Of All Lots Of Max Health Hydro Pineapple Burn By John Nguyen (JONGU 4308), An Ebay Seller Due To Presence Of Undeclared Sibutramine
, The National Agency for Food and Drug Administration and Control (NAFDAC) has received information from US FDA on the recall of all lots of Max health Hydro Pineapple Burn manufactured by Jongu 4308 because FDA analysis has found the product to contain undeclared sibutramine. The presence of sibutramine in Max health Hydro Pineapple Burn […]
Public Alert No: 0035/2021 – Recall Of Products Labelled As Infant Formulas By Able Groupe Due To Insufficient Iron Levels And Failure To Meet Fda Requirements
, The National Agency for Food and Drug Administration and Control (NAFDAC) has received information from US FDA on the recall of certain infant Formulas manufactured by Able Groupe due to insufficient Iron levels and not meeting other FDA requirements. The recalled products were sold under the brand names HiPP, Holle, Bioland and Kendamil. The […]
Public Alert: 032/2021 – Palisades Park HIS Issues Voluntary Recall of Miss Slim Due to the Presence of Undeclared Sibutramine
, The National Agency for Food and Drug Administration and Control has been informed by the U.S. Food and Drug Administration that Palisades Park, NJ, HIS is voluntarily recalling all lots and all presentations of Miss Slim (10 count & 30 count capsules) to the consumer level. The recall of Miss Slim was due to […]
Public Alert No:31/2021 – Johnson & Johnson Consumer Inc. Issues Voluntary Recall of Specific NEUTROGENA® and AVEENO® Aerosol Sunscreen Products Due to the Presence of Benzene
, The National Agency for Food and Drug Administration and Control has been informed by US FDA that Johnson & Johnson Consumer Inc. (JJCI) is voluntarily recalling all lots of five NEUTROGENA® and AVEENO® aerosol sunscreen product lines to the consumer level. The recall was due to low levels of benzene identified in some samples […]
Public Alert No. 030/2021 – Alert on Recall of All Unexpired Lots of Alpha Male Plus Male Enhancer fruit chews by Alpha Male Plus Due to the Presence of Undeclared Tadalafil and Sildenafil
, The National Agency for Food and Drug Administration and Control has been informed by the U.S. Food and Drug Administration that Tucson, AZ, Alpha Male Plus is voluntarily recalling all lots of unexpired Alpha Male Plus Male Enhancer fruit chews. The result of analysis by FDA found the product to contain undeclared tadalafil, an […]
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 […]
Public Alert No.027/2021- Statins: Drug Safety Communication – US Food And Drug Administration (FDA) Requests Removal Of Strongest Warning Against Using Cholesterol-Lowering Statins During Pregnancy
, The National Agency for Food and Drug Administration and Control (NAFDAC) has been informed by the U.S FDA about revisions to the prescribing information of the entire class of statin medicines, regarding their use in pregnancy. These changes include removing the contraindication against using these medicines in all pregnant patients. A contraindication is FDA’s […]
