Consumers with questions regarding this recall can contact Sun Pharma by calling 1-800-818-4555 Monday through Friday between 8:00 am to 5:00 pm EST or e-mailing drug.safetyUSA@sunpharma.com. The current recall applies to metformin tablets between 500 mg and 750 mg, sold under the brand name Time-Cap Labs Inc. U.S. health regulators are telling five drugmakers to recall versions of the widely used diabetes medication after testing revealed elevated levels of a contaminant linked to cancer in several lots. FDA Requests Metformin Recall by Five Drug Manufacturers The information provided on this Web site should not be construed as medical instruction. Some lots of the diabetes medication metformin were placed under voluntary recall on Wednesday by U.S. distributor, Bayside Pharmaceuticals. We have created a site to share drug recall information. Several other generic drugmakers were also asked to recall metformin products due to similar NDMA concerns last May. Metformin – Safety update. "GMP news" is a Portal about international GMP Standard for pharmaceutical professionals and specialists, managers, and students. Back in November 2017, the U.S. subsidiary carried out a nationwide voluntary recall of two lots of Riomet (metformin oral solution). Marksans expanded its voluntary recall to include 76 additional unexpired lots of metformin ER tablets (500 mg and 750mg) labeled as Time-Cap Labs. ... the drugmaker pulled 500- and 1,000-milligram versions of extended-release metformin … Sun Pharmaceutical Industries, Inc., a wholly owned subsidiary of Sun Pharmaceutical Industries Ltd. is voluntarily recalling one lot of RIOMET ER™ (metformin hydrochloride for extended-release oral suspension), 500 mg per 5 mL to the consumer level. The product has been manufactured at Sun Pharma’s Mohali-based manufacturing plant and is being recalled by its US-based subsidiary. RIOMET ER™ (metformin hydrochloride for extended-release oral suspension) is a prescription oral medication indicated as an adjunct to diet and exercise to improve glycemic control in adults and pediatric patients 10 years of age and older with type 2 diabetes mellitus. To date, SUN PHARMA has not received any reports of adverse events related to this recall. 11 Oct 2020, 18:47; ... while the recall applies to metformin tablets between 500 mg and 750 mg. At Magellan Rx Management, we want to help you get the best possible care. To date, Sun Pharma has not received any reports of adverse events related to this recall. To date, SUN PHARMA has not received any reports of adverse events related to this recall. The latest manufacturer to recall the prescription is Sun Pharma, which late last month, announced a voluntary recall of one lot of its extended-release (ER) metformin hydrochloride oral suspension (Riomet ER). On Oct. 9, 2020, the FDA provided an update to this recall to include two voluntary recalls by Marksans Pharma and Sun Pharmaceutical Industries for extended release metformin due to … September 23, 2020 -- Sun Pharmaceutical Industries, Inc. (Sun Pharma), a wholly owned subsidiary of Sun Pharmaceutical Industries Ltd. is voluntarily recalling one lot of Riomet ER™ (metformin hydrochloride for extended-release oral suspension), 500 mg per 5 mL to the consumer level. The product is a liquid that is packaged in a 16-oz. Sun Pharma recalls 747 bottles of generic diabetes drug in US market: USFDA The US health regulator has classified it as a Class-II recall, which is initiated in a "situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote". Each carton contains one bottle of drug pellets, one bottle of diluent, and one dosing cup. 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