Every recall we track for Biogen MA Inc. — 2 in all, all from 2020 — plus the complaints and injury reports the public filed about them.
Biogen recalls Vumerity (diroximel fumarate) 231mg capsules due to failed dissolution testing. Affected bottles: 106-count and 120-count, Rx only. No remedy specified in recall notice.
Biogen recalls Tecfidera 240mg capsules due to a manufacturing issue that may have led to contaminated product distribution. Affected lots were distributed despite in-process rejection.
2 recalls from Biogen MA Inc. are on record with U.S. safety agencies, from 2020.
Biogen MA Inc. recalls Vumerity (diroximel fumarate) delayed-release capsule, 231 mg, packaged in a) 106-count bottle, b)120-count bottle, Rx, dated Dec 9, 2020. Every Biogen MA Inc. recall is listed on this page, newest first.
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
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