Public Alert No. 006/2022- Public Alert On Class 2 Recall Of IKERVIS 1MG/ML Eye Drops, Emulsion
, The National Agency for Food and Drug Administration and Control (NAFDAC) is notifying healthcare providers that Medicines & Healthcare products Regulatory Agency (MHRA) and the Health Science Authority Singapore is recalling one lot each of IKERVIS 1 mg/mL eye drops manufactured by SANTEN Oy (trading as Santen UK Limited) and Santen Pharmaceutical Asia Pte Ltd. […]
Public Alert No. 005/2022- Recall of Dermaved Sensitive Cream (Unlicensed Medicine)
, The National Agency for Food and Drug Administration and Control is informing healthcare providers that Medicines & Healthcare products Regulatory Agency (MHRA) in conjunction with Dermaved is recalling Dermaved Sensitive Cream due to presence of clobetasol propionate (0.001% w/w). Clobetasol propionate is a strong steroid and it is an active ingredient in Prescription […]
Public Alert No: 004/2022 – Recall Of Bake Crafters -Maple Waffle Wg Chicken Sausage Sandwich Due To Potential Listeria Monocytogenes Contamination
, The National Agency for Food and Drug Administration and Control (NAFDAC) has received information from US FDA on the voluntary recall of Bake Crafters Maple Waffle WG Chicken Sausage manufactured by Bake Crafters, USA due to potential Listeria monocytogenes contamination. Consumption of the contaminated product may produce symptoms of listeriosis, which can take up […]
Public Alert 003/2022 – Alert on Recall of Clobetasol Propionate Ointment USP, 5%, 60g Tubes by Taro Pharmaceuticals Incorporation U.S.A, Due to Microbial Contamination
, The National Agency for Food and Drug Administration and Control (NAFDAC) has received information from US FDA that Taro Pharmaceuticals U.S.A., Inc. is voluntarily recalling one (1) lot of Clobetasol Propionate Ointment USP, 0.05% packaged in 60 g tubes, to the consumer level due to the presence of Ralstonia pickettii bacteria which was discovered by the […]
Public Alert 002/2022 – Alert on Recall of Lidocaine HCI Topical Solution USP, 4% by Teligent Pharma, Due to Super Potency
, The National Agency for Food and Drug Administration and Control (NAFDAC) has received information from US FDA that Teligent Pharma, Inc. is voluntarily recalling two lots of Lidocaine HCl Topical Solution USP 4%, 50ml in a screw cap glass bottle. The product is being recalled because the firms testing has found it to be super […]
Public Alert No: 001/2022 – Efficient Laboratories, Inc. Expands Voluntary Nationwide Recall to Consumers to Include Twelve Additional Lots of Rompe Pecho CF, Rompe Pecho EX, Rompe Pecho MAX, and Rompe Pecho DM Sold in 2019 Due to Microbial Contamination Concerns
, The National Agency for Food and Drug Administration and Control (NAFDAC) has been informed by U.S Food and drug Administration (FDA) that Efficient Laboratories Miami, Florida. is expanding its voluntary recall to consumers to include twelve lots of Rompe Pecho CF, Rompe Pecho EX, Rompe Pecho MAX, and Rompe Pecho DM due to microbial […]
Public Alert No.0048/2021 Food Recall Warning – Amara Brand Organic Smoothie Melts – Carrot Raspberry Recalled Due To Plastic Pieces
, The National Agency for Food and Drug Administration and Control (NAFDAC) has been informed by Canada’s Food and Drugs Act and Regulations that Pata-Foods Inc. Dba Amara, Ottawa, Canada, on 31st October, 2021, recalled its Organic Smoothie Melt Carrot Raspberry due to contamination, the product, which contain pieces of plastic has been linked to […]
Public Alert No.0047/2021 Recall Of Substandard Lefin Pediatric Suspension Manufactured By M/S. Leama Chemi Pharma (PVT) Ltd
, The National Agency for Food and Drug Administration and Control (NAFDAC) has been informed by Drug Regulatory Authority of Pakistan (DRAP) about a recent recall of Lefin Pediatric Suspension manufactured by M/s Leama Chemi Pharma (Pvt) Limited for being Substandard. Lefin Pediatric suspension is a brand of Paracetamol use for the relief of mild […]
Public Alert No.0046/2021 – American Screening LLC Issues A Voluntary Nationwide Recall Of American Screening Hand Sanitizer Packaged In 8 Oz Bottles Because They Resemble Beverage Containers
, The National Agency for Food and Drug Administration and Control (NAFDAC) has been informed by U.S Food and Drug Administration (FDA) that American screening LLC issues a voluntary recall of American screening hand sanitizer packaged in 8 oz bottles because they resemble beverage containers. Risk Associated Ingesting hand sanitizer, which is intended for topical […]
Public Alert No. 045/2021- Alert on the Voluntary Recall of Specific Lots of Odor- Eaters® Spray Powder and Odor-Eaters® Stink Stoppers® Spray Due to Benzene Contamination
, The National Agency for Food and Drug Administration and Control has been informed by the U.S. Food and Drug Administration (FDA) that Odor-Eaters®, owned by Blistex Inc., is voluntarily recalling a total of forty-one lots of two Odor-Eaters® spray products due to the presence of benzene. Internal testing identified low levels of benzene contamination […]
