PlainRecalls

Biomet Microfixation, LLC

Compiled from official public sources by the publisher.

19 recalls on record · Latest: May 24, 2017

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Agency notice ledger

Federal filing book Biomet Microfixation, LLC LIGHT-BOOK · SINGLE-AGENCY

#836 of 14,151 · 19 notices · 0.018% archive

  • BOOK 19 notices
  • RANK #836 of 14,151
  • SHARE 0.018% archive
  • AGENCY FDA Devices (19)
  • CAT medical devices
  • CATS 1 category
  • LATEST May 24, 2017
  • PHOTO Abbott

Nearest notice-volume peer: Abbott (0 notice gap)

Biomet Microfixation, LLC accounts for about 0.018% of the 104,423-notice archive on 19 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Biomet Microfixation, LLC's standing among 14,151 recalling firms

Biomet Microfixation, LLC ranks 836th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Biomet Microfixation, LLC vs all firms by recall-notice count

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

19 836th of 14151 higher than 13,281 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 · 2026-09-14

Biomet Microfixation, LLC in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Biomet Microfixation, LLC holds about 0.018% of archive notices alongside 19 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate May 24, 2017

Biomet Microfixation TraumaOne System Surgical Tray - Model # 46-1600
FDA Devices Moderate Sep 14, 2016

Hard Tissue Replacement (HTR) Implant, Rx only, for use in single procedure only. Custom made. HTR polymer implants are intended for bone replacement/augmentation for treatment of craniofacial voids/defects resulting from disease, injury, or surgical trauma.
FDA Devices Moderate Oct 28, 2015

Neuro Combo Set Case The cases hold surgical instrumentation in place during handling and storage.
FDA Devices Moderate Oct 28, 2015

Thinflap System Case The cases hold surgical instrumentation in place during handling and storage.
FDA Devices Moderate Dec 17, 2014

Total Temporomandibular Joint Replacement System- 50mm Rt Standard Ti Mand Reconstruction of the temporomandibular joint
FDA Devices Moderate Dec 17, 2014

Total Temporomandibular Joint Replacement System- 45mm Rt Narrow Ti Mand Reconstruction of the temporomandibular joint
FDA Devices Moderate Dec 17, 2014

Total Temporomandibular Joint Replacement System- 50mm Rt Narrow Ti Mand Reconstruction of the temporomandibular joint
FDA Devices Moderate Dec 17, 2014

Total Temporomandibular Joint Replacement System- 50mm Rt Stand Off Ti Mand Reconstruction of the temporomandibular joint
FDA Devices Moderate Dec 17, 2014

Total Temporomandibular Joint Replacement System- 45mm Lft Standard Ti Mand Reconstruction of the temporomandibular joint
FDA Devices Moderate Dec 17, 2014

Total Temporomandibular Joint Replacement System- 50mm Lft Narrow Ti Mand Reconstruction of the temporomandibular joint
FDA Devices Moderate Dec 17, 2014

Total Temporomandibular Joint Replacement System- 50mm Lft Standard Ti Mandi Reconstruction of the temporomandibular joint
FDA Devices Moderate Dec 17, 2014

Total Temporomandibular Joint Replacement System- 55mm Lft Standard Ti Mand Reconstruction of the temporomandibular joint
FDA Devices Moderate Dec 17, 2014

Total Temporomandibular Joint Replacement System- 45mm Lft Narrow Ti Mand
FDA Devices Moderate Dec 17, 2014

Total Temporomandibular Joint Replacement System- 45mm Rt Stand Off TI Mand Reconstruction of the temporomandibular joint
FDA Devices Moderate Dec 17, 2014

Total Temporomandibular Joint Replacement System- 55mm Rt Standard Ti Mand Reconstruction of the temporomandibular joint
FDA Devices Moderate Dec 17, 2014

Total Temporomandibular Joint Replacement System- 45mm Rt Standard TI Mand Reconstruction of the temporomandibular joint
FDA Devices Moderate Dec 17, 2014

Total Temporomandibular Joint Replacement System- 45mm Lft Stand Off Ti Mand Reconstruction of the temporomandibular joint
FDA Devices Moderate Dec 17, 2014

Total Temporomandibular Joint Replacement System- 50mm Lft Stand Off Ti Mand Reconstruction of the temporomandibular joint
FDA Devices Moderate Sep 10, 2014

Biomet Microfixation Temporomandibular Joint (TMJ) Patient Matched Left Fossa Part# CP751506 The Total Temporomandibular Joint (TMJ) replacement system is implanted in the jaw to functionally reconstruct a diseased and/or damaged temporomandibular joint. The Total TMJ replacement system is a two-component system comprised of mandibular condyle and a glenoid fossa components. Both components are available in multiple stock sizes as right and left specific designs and are attached to the bones

Biomet Microfixation, LLC holds a measurable archive slice

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

Similar recall count

Nearest multi-notice firms by distinct-event totals (19 here).

Abbott 19 Abbott Gmbh & Co. Kg 19 Abbott Medical Optics Inc. (Amo) 19 Adm Milling 19 Advance Pierre N 19

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Abbott 19 Abbott Gmbh & Co. Kg 19 Abbott Medical Optics Inc. (Amo) 19 Amo Puerto Rico Manufacturing, Inc. 19

Frequently Asked Questions

How many federal recall notices name Biomet Microfixation, LLC? ▼
PlainRecalls indexes 19 distinct federal recall events naming Biomet Microfixation, LLC, 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 Biomet Microfixation, LLC sit among other recalling firms? ▼
Biomet Microfixation, LLC ranks #836 of 14,151 by distinct recall-event count among 14,151 firms in this archive (94th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Biomet Microfixation, LLC's notices? ▼
FDA Devices accounts for 19 of this firm's 19 indexed notices.
What product category dominates Biomet Microfixation, LLC's filing book? ▼
Filings for Biomet Microfixation, LLC span 1 product category, led by medical devices. 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.
Biomet Microfixation, LLC: 19 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Biomet Microfixation, LLC; individual notices remain authoritative on each linked recall page.

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