Product Recalls: July 17, 2019 – August 14, 2019
Health Letter, September 2019
Note: Never stop taking a drug that appears on the product recall list without first talking to your doctor or pharmacist. Most recalls are limited to a single manufacturer and may not be related to the version of a particular drug you are taking. If a recall does relate to the version of the drug you are taking, you should not stop taking the drug until you discuss an alternative treatment with your doctor or pharmacist.
CLASS II
Atorvastatin calcium tablets, 80 mg, 90- or 500-count bottles. Manufactured by: Alkem Laboratories, Ltd.
Divalproex sodium extended-release tablets, 250 mg, 100-count unit-dose carton. Manufactured by Dr. Reddy’s Laboratories Ltd.
Doxycycline hyclate tablets, 100 mg, 30 tablets per carton (3 x 10 Unit Dose Blisters). Distributed by: American Health Packaging.
Kaitlib Fe norethindrone and ethinyl estradiol chewable tablets, 0.8 mg/0.025 mg and ferrous fumarate. Manufactured by: Lupin Limited.
Lisinopril and hydrochlorothiazide tablets, 20 mg/12.5 mg, 500-count bottle. Manufactured for: Lupin Pharmaceuticals, Inc.
Temozolomide capsules; 5, 20, 100, 140, 180 or 250 mg; 5- or 14-count bottle. Manufactured by: Deva Holding A.S.
For more information about the drug recalls listed above, please visit http://www.accessdata.fda.gov/scripts/ires/index.cfm.
CONSUMER PRODUCTS
For a list of recent recalls of consumer products, please visit the Consumer Product Safety Commission website at http://www.cpsc.gov/en/Recalls/.