Which brands of losartan have been recalled?
The affected lots of the voluntary recall by Legacy Pharmaceutical Packaging are the following: NDC 68645-494-54, losartan potassium tablets USP 50 mg, 30 count, Legacy Lot 180190, expires on 10/2020. NDC 68645-494-54, losartan potassium tablets USP 50 mg, 30 count, Legacy Lot 180191, expires on 10/2020.
What is the latest recall on losartan?
In November, the FDA announced a voluntary recall of losartan potassium/hydrochlorothiazide, 100 mg/25 mg tablets in 1,000-count plastic bottles, NDC 0781-5207-10, Lot number JB8912, Exp. Date 06/2020.
Has losartan been recalled 2021?
PD-Rx Pharmaceuticals Inc. is recalling 576 bottles of losartan potassium tablets because they contain trace amounts of the nitrosamine impurity NMBA, according to the May 5, 2021, US Food and Drug Administration (FDA) Enforcement Report.
Is losartan OK to take now?
Conclusion: Losartan in the form of Lozap or Lozap is a safe and effective treatment of patients with hypertensive disease.
Is there a recall on losartan blood pressure pills 2022?
The FDA designated them Class II on May 3, 2022. Drugs affected by Class II recalls may cause temporary or medically reversible adverse health consequences if used. While remote, a possibility of serious harm also exists. Losartan is a prescription medication used to treat high blood pressure.
Are all hydrochlorothiazide tablets recalled?
To assist you in the care of your patients, we would like to alert you to the recall of all batches of irbesartan 75 mg, 150 mg and 300 mg tablets and irbesartan and hydrochlorothiazide 150 mg/12.5 mg and 300 mg/12.5 mg tablets on Oct. 14, 2021.
Is losartan still on recall in 2022?
What is the problem with losartan?
Since losartan is a medication used to lower blood pressure, sometimes it can lower blood pressure too much, which can cause dizziness or even fainting. In certain cases, it can reduce blood flow to the kidneys, causing kidney failure. In addition, it can cause high blood potassium (hyperkalemia) (UpToDate, n.d.).
What is a voluntary drug recall?
A recall is a voluntary action taken by a company at any time to remove a defective drug product from the market. The list below includes voluntary recalls in which public notification has been issued. See FDA’s role in drug recalls for more information. See Recalls, Market Withdrawals, & Safety Alerts for all FDA-regulated products.
Why are some medical devices on the recall list?
These products are on the list because there is a reasonable chance that they could cause serious health problems or death. Use the yearly lists to find information about Class I medical device recalls and some Class II and III recalls of interest to patients. The links give details about what to do if you own or use one of these products.
Which over-the-counter drugs have been recalled in 2018?
The recall involves 31 different over-the-counter drugs purchased on or after June 1, 2018 that are unexpired from the following brands: Medi-First, Medi-First Plus, Medique, Dover, Otis Clapp, and Ecolab.
Is there a recall on varenicline?
FDA Alerts Health Care Professionals and Patients to a Voluntary Recall of Chantix (varenicline) to the Warehouse Level July 2, 2021 — FDA is alerting patients and health care professionals to Pfizer’s voluntary recall of nine lots of the smoking cessation drug… July 2, 2021