(UnitedVoice.com) – Our medications should keep us healthy, not harm us. That’s why it’s important to stay up-to-date on prescription drug recalls. Here are some recent recalls from major drug manufacturers.
Denton Pharma, Inc. dba Northwind Pharmaceuticals Voluntarily Recalls All Unexpired Lots of its Ranitidine Tablets and Ceases Distribution, Due to Possible Presence of N-nitrosodimethylamine (NDMA) Impurity https://t.co/fm4tZIcjzy pic.twitter.com/EckwZaACei
— U.S. FDA (@FDArecalls) January 8, 2020
Popular heartburn drug Ranitidine has been involved with recalls since November. Now another manufacturer has recalled the medicine because of possible carcinogenic impurities.
Denton Pharma, Inc. dba Northwind Pharmaceuticals, has issued a voluntary recall of all 150mg and 300 mg Ranitidine tablets. The recall is part of a larger one because of the presence or potential presence of NDMA.
NDMA is a chemical that can form naturally during industrial processes. It’s known to cause cancer when present in higher than recommended levels.
— U.S. FDA (@FDArecalls) January 13, 2020
Taro Pharmaceutical Industries has issued a recall of the epilepsy and bipolar medication Lamotrigine. The recall is due to the presence of Enalapril Maleate, a heart and blood pressure medication, which was caused by cross-contamination.
The only dose included in the recall right now is Lamotrigine 100mg, lot No. 331771, with an expiration date of June 2021.
RECALL: Depression medication Mirtazapine recalled due to label error on declared strength https://t.co/KzPtCN77He
— KTVU (@KTVU) January 3, 2020
Aurobindo Pharma has recalled depression medicine Mirtazapine, sold under the brand name of Remeron because some bottles might have the wrong pills.
It was discovered that bottles labeled as 7.5 mg might actually contain 15 mg tablets. The official recall states that “Taking a higher dose than expected may increase risk of sedation, agitation, increased reflexes, tremor, sweating, dilated pupils, gastrointestinal distress, nausea, constipation and more.”
The pills involved in the recall are from lot number 03119002A3 with an expiration date of 03/2022.
Consumers who have questions are being asked to call Aurobindo Pharma at 1-566-850-2876 and choose option 2.
Copyright 2020, UnitedVoice.com