PlainRecalls

Exactech, Inc.

Compiled from official public sources by the publisher.

211 recalls on record · Latest: Mar 18, 2026

Subscribe to new Exactech, Inc. recalls (RSS)

Agency notice ledger

Federal filing book Exactech, Inc. HEAVY-BOOK · SINGLE-AGENCY

#64 of 14,151 · 211 notices · 0.202% archive

  • BOOK 211 notices
  • RANK #64 of 14,151
  • SHARE 0.202% archive
  • AGENCY FDA Devices (211)
  • CAT medical devices
  • CATS 1 category
  • LATEST Mar 18, 2026
  • PHOTO Medtronic Vascular

Nearest notice-volume peer: Medtronic Vascular (0 notice gap)

Exactech, Inc. accounts for about 0.202% of the 104,423-notice archive on 211 distinct filings — a heavy 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 Exactech, Inc. compares to 14,151 recalling firms

Exactech, Inc. ranks 64th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Exactech, Inc. vs all firms by recall-notice count

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

211 64th of 14151 higher than 14,086 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

Exactech, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Exactech, Inc. holds about 0.202% of archive notices alongside 211 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Sep 19, 2012

REF 101-45-30***NOVATION MODULAR DRILL BIT LENGTH: 30mm, DIAMETER 4.5mm***Use with 30mm Screw***STERILE***EXACTECH 2320 NW 56th Court, Gainesville, FL 32653***. To assist the surgeon in the implantation of Novation Hip system components in according to a conventional technique for hemi & total hip arthroplasty. Specifically, these instruments are reusable, surgically invasive, and intended for transient use.
FDA Devices Moderate Sep 12, 2012

OPTETRAK LOGIC TIBIAL INSERT POSTERIOR STABILIZED***Match Component Colors 6 YELLOW, 11mm, Use with LOGIC Femoral and Tibial Components***REF 02-012-35-6011. There are three product sizes being recalled, 11mm, 13mm, 15mm. All other information is the same. The Optetrak Logic Total Knee System is indicated for use in skeletally mature individuals undergoing primary surgery for total knee replacement due to osteoarthritis, osteonecrosis, rheumatoid arthritis, and/or post-traumatic degenerati
FDA Devices Moderate Aug 29, 2012

OPTETRAK LOGIC Proximal Tibial Spacer & Screws (2) 2.5 LT BLUE Size 2.5, 8mm***STERILE***Match insert/spacer/tray color. Use with LOGIC Tibial Components. REF 02--012-42-2508. The Optetrak Comprehensive Knee Systems are indicated for use in skeletally mature individuals undergoing primary surgery for total knee replacement due to osteoarthritis, osteonecrosis, rheumatoid arthritis, and/or post-traumatic degenerative problems. They are also indicated for revision of failed previous reconstruct
FDA Devices Moderate Aug 8, 2012

Octane-C Cervical, 6¿ Lordotic Intended for anterior cervical spine intervertebral body fusion procedures at one level (C3-C7).
FDA Devices Moderate Aug 8, 2012

Equinoxe Fixed Angle Replicator Plate Intended for Primary and Reverse Total Shoulder Arthroplasty.
FDA Devices Moderate Aug 8, 2012

Equinoxe Reverse Glenosphere Locking Screw Intended for Primary and Reverse Total Shoulder Arthroplasty.
FDA Devices Moderate Aug 8, 2012

Equinoxe Anatomic Replicator Plate Intended for Primary and Reverse Total Shoulder Arthroplasty
FDA Devices Moderate Aug 8, 2012

Equinoxe Reverse Compression Screw Intended for Primary and Reverse Total Shoulder Arthroplasty.
FDA Devices Moderate Aug 8, 2012

Equinoxe Reverse Shoulder Fracture Adapter Tray Screw Intended for Primary and Reverse Total Shoulder Arthroplasty.
FDA Devices Moderate Aug 1, 2012

Product is labeled in part: "***OPTETRAK RBK***TIBIAL TRAY***FINNED, CEMENTED***CoCr Alloy***SIZE 2F/1T***REF 260-04-21***Exactech Gainesville, FL 32653-1630***. The Exactech Optetrak RBK Total Knee System is indicated for use in skeletally mature individuals undergoing primary surgery for knee pain and disability due to rheumatoid arthritis, osteoarthritis, traumatic arthritis, polyarthritis, collagen disorders and/or avascular necrosis of the femoral condyle, post-traumatic loss of the jo
FDA Devices Moderate Aug 1, 2012

Product is labeled in part: "***OPTETRAK***TIBIAL TRAY***TRAPEZOID CEMENTED***Ti Alloy*** SIZE 1F/1T, 2F/1T***FOR CEMENTED USE ONLY***Exactech, Gainesville, FL 32653-1630.***REF 204-04-21***". The Optetrak Comprehensive Knee Systems are indicated for use in skeletally mature individuals undergoing primary surgery for total knee replacement due to osteoarthritis, osteonecrosis, rheumatoid arthritis and/or post-traumatic degenerative problems. They are also indicated for revision of failed pre

Exactech, Inc. carries an outsized archive share

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 (211 here — heavy-book).

Medtronic Vascular 211 Philips Medical Systems Nederland B.v. 209 Volkswagen 207 Integra LifeSciences Corp. 217 Teleflex Medical 204

Similar medical devices volume

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

Medtronic Vascular 211 Philips Medical Systems Nederland B.v. 209 Integra LifeSciences Corp. 217 Teleflex Medical 204

Frequently Asked Questions

How many federal recall notices name Exactech, Inc.? ▼
PlainRecalls indexes 211 distinct federal recall events naming Exactech, 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 Exactech, Inc. sit among other recalling firms? ▼
Exactech, Inc. ranks #64 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Exactech, Inc.'s notices? ▼
FDA Devices accounts for 211 of this firm's 211 indexed notices.
What product category dominates Exactech, Inc.'s filing book? ▼
Filings for Exactech, Inc. 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.
Exactech, Inc.: 211 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 Exactech, Inc.; individual notices remain authoritative on each linked recall page.

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