Mylan LLC. recalls Temozolomide Capsules, 250 mg, 5-count bottles, Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 USA, NDC 0378
Recalled February 1, 2017 · FDA recall D-0444-2017 · Mylan
Hazard
Failed Tablet/Capsule Specifications: customer complaints of broken or crushed capsules, resulting in loose powder in the bottle. · FDA Class II
Units
588 bottles
Sold at
Nationwide in the USA
Description
Failed Tablet/Capsule Specifications: customer complaints of broken or crushed capsules, resulting in loose powder in the bottle.
Product
Temozolomide Capsules, 250 mg, 5-count bottles, Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 USA, NDC 0378-5265-98.
Manufacturer(s)
Mylan LLC.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →