Public Alert No. 018/2020-Rwanda FDA Recalls Chinese-made face masks over non-compliance with regulatory standards
, The National Agency for Food and Drug Administration and Control has been informed that the Rwandan Food and Drug Authority (FDA) has recently recalled Chinese-made face masks, YK01 FFP2 due to insufficient particle filter retention of the material and non-compliance with regulatory standards. Face-masks are in high demand due to the Covid-19 pandemic as […]
Public Alert: 013/2020-Recall of Amlodipine 10mg Batch Number GY0128 by Accord Healthcare Limited UK
, The National Agency for Food and Drug Administration and Control has received information from United Kingdom Medicine and Healthcare Products Regulatory Agency (MHRA), of a voluntary recall of one batch of high blood pressure medication, Amlodipine 10mg tablets manufactured by Accord Healthcare Limited. The company took the decision to recall the blood pressure medication […]
Public Alert No: 014/2020- Recall of Liquid Fruit Grape Juice product code 27327 by South Africa Foods Company
, The National Agency for Food and Drug Administration and Control (NAFDAC) has received report that South Africa Pioneer Foods Company has voluntarily recalled Liqui Fruit Red Grape Juice 330ml can with product code 27327. Updated Report available reveal that Pioneer Foods has confirmed that Liqui Fruit Red Grape Juice 330ml cans related to the […]
Public Alert No. 012/2020-Presence of Suspected Falsified SA’A TRIM (Sulfamethoxazole) circulating in an illicit market in Chad
, The National Agency for Food and Drug Administration and Control has received information from WHO that a stakeholder DIFAEM has confirmed the presence of Suspected Falsified SA’A TRIM (Sulfamethoxazole) circulating in an illicit market in Chad. The active pharmaceutical ingredients of the Genuine SA’ATRIM are a combination of two antibiotics (Sulfamethoxazole BP 400MG, Trimethoprim […]
Regulatory Authorities Recall Alcohol Based Hand Sanitizers Containing Methanol
, The National Agency for Food and Drug Administration and Control (NAFDAC) has received information from US FDA of the recall of all alcohol- based hand sanitizer products that are labelled to contain ethanol (also known as ethyl alcohol) but that have tested positive for methanol. In a another notification, Rwanda Food and Drugs Authority (RFDA) has […]
Public Alert No. 0010/2020 Recall of FARO Table Water 750ml Due to Presence of Particles
, The National Agency for Food and Drug Administration and Control (NAFDAC) has directed Adama Beverages Limited to recall FARO Table Water 750ml as a precautionary step pending conclusion of investigation by the Agency. A consumer complaint was received by NAFDAC on 3rd September, 2020 on the presence of particles in one batch (B179). The […]
Recall Of DDAVP® Nasal Spray 10mcg/0.1ml, Desmopressin Acetate Nasal Spray 10mcg/0.1ml, STIMATE® Nasal Spray 1.5mg/ml Due To Superpotency
, The National Agency for Food and Drug Administration and Control has received information from the US FDA that Ferring Pharmaceuticals US is voluntarily recalling all lots of DDAVP® Nasal Spray 10 mcg/0.1mL, Desmopressin Acetate Nasal Spray 10 mcg/0.1mL, and STIMATE® Nasal Spray 1.5 mg/mL to the consumer level. These products are being recalled due to superpotency […]
Recall Of Heparin Sodium Compounded Products By SCA Pharmaceuticals
, The National Agency for Food and Drug Administration and Control has received information from the US FDA about the voluntary recall of Ten (10) lots of heparin sodium products by SCA pharmaceutical. The recall is due to presence of incorrect preservative (Benzyl Alcohol). Whereas the labelling of the products listed methyl paraben and propyl […]
Voluntary Recall Of Two Lots Of Dexmedetomidine Hydrochloride Injection Due To Cross-Contamination Of Lidocaine
, The National Agency for Food and Drug Administration and Control (NAFDAC) has received information from the US FDA about the voluntary recall of two lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200mcg/50mL (4mcg/mL), 50mL fill in a 50mL vial by Fresenius Kabi, USA Fresenius Kabi initiated this recall due to the possibility […]
Recall Of Daptomycin For Injection 500mg/Vial By Mylan
, The National Agency for Food and Drug Administration and Control (NAFDAC) has received information from the US FDA about voluntary recall of one lot of Daptomycin for Injection, 500 mg/vial by Mylan institutional LLC. The recall is due to the presence of particulate matter found in one single-dose vial manufactured by Mylan Laboratories Limited’s […]
