PlainRecalls

Biogen Ma Inc.

Compiled from official public sources by the publisher.

2 recalls on record · Latest: Dec 23, 2020

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Agency notice ledger

Federal filing book Biogen Ma Inc. LIGHT-BOOK · SINGLE-AGENCY

#4,432 of 14,151 · 2 notices · 0.002% archive

  • BOOK 2 notices
  • RANK #4,432 of 14,151
  • SHARE 0.002% archive
  • AGENCY FDA Drug (2)
  • CAT drugs
  • CATS 2 categories
  • LATEST Dec 23, 2020
  • PHOTO 3M Company

Nearest notice-volume peer: 3M Company (0 notice gap)

Biogen Ma Inc. accounts for about 0.002% of the 104,423-notice archive on 2 distinct filings — a light share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

How Biogen Ma Inc. compares to 14,151 recalling firms

Biogen Ma Inc. ranks 4,432nd of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Biogen Ma Inc. vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

2 4432nd of 14151 higher than 8,037 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Biogen Ma Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Biogen Ma Inc. holds about 0.002% of archive notices alongside 2 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Drug Moderate Dec 23, 2020

Vumerity (diroximel fumarate) delayed-release capsule, 231 mg, packaged in a) 106-count bottle, b)120-count bottle, Rx only, Manufactured for: Biogen Inc., Cambridge, MA 02142, NDC 64406-020-01
FDA Drug Low Jul 15, 2020

Tecfidera (dimethyl fumarate) delayed-release capsules, 240 mg, 60-count bottle, Rx only, Manufactured by: Biogen Inc., Cambridge, MA 02142, NDC 64406-006-02

Biogen Ma Inc. is a small archive contributor

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar drugs volume

Nearest multi-notice firms that share this firm's dominant product category.

Aaa Cosmetica, Sa de Cv 2 Abc Sales 1 Inc 2 Abrams Royal Pharamacy 2 Acme United, of Rocky Mount, North Carolina 2

Frequently Asked Questions

How many federal recall notices name Biogen Ma Inc.? ▼
PlainRecalls indexes 2 distinct federal recall events naming Biogen Ma Inc., aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Biogen Ma Inc. sit among other recalling firms? ▼
Biogen Ma Inc. ranks #4,432 of 14,151 by distinct recall-event count among 14,151 firms in this archive (57th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Biogen Ma Inc.'s notices? ▼
FDA Drug accounts for 2 of this firm's 2 indexed notices.
What product category dominates Biogen Ma Inc.'s filing book? ▼
Filings for Biogen Ma Inc. span 2 product categories, led by drugs. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Biogen Ma Inc.: 2 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Drug). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Biogen Ma Inc.; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026