PlainRecalls

Orthosensor, Inc.

Compiled from official public sources by the publisher.

7 recalls on record · Latest: Oct 17, 2018

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Agency notice ledger

Federal filing book Orthosensor, Inc. LIGHT-BOOK · SINGLE-AGENCY

#1,996 of 14,151 · 7 notices · 0.007% archive

  • BOOK 7 notices
  • RANK #1,996 of 14,151
  • SHARE 0.007% archive
  • AGENCY FDA Devices (7)
  • CAT medical devices
  • CATS 1 category
  • LATEST Oct 17, 2018
  • PHOTO A I Foods Corporation

Nearest notice-volume peer: A I Foods Corporation (0 notice gap)

Orthosensor, Inc. accounts for about 0.007% of the 104,423-notice archive on 7 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 →

Orthosensor, Inc.'s standing among 14,151 recalling firms

Orthosensor, Inc. ranks 1,996th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

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

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

7 1996th of 14151 higher than 12,091 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 · 2026-09-15

Orthosensor, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Orthosensor, Inc. holds about 0.007% of archive notices alongside 7 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Oct 17, 2018

OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Left, REF ZBH-PSNCREF311-L.
FDA Devices Moderate Oct 17, 2018

OrthoSensor VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Right, REF ZBH-PSNCRGH712-R.
FDA Devices Moderate Oct 17, 2018

OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Right, REF ZBH-PSNCREF311-R.
FDA Devices Moderate Oct 17, 2018

OrthoSensor VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Right, REF ZBH-PSNCRCD39-R.
FDA Devices Moderate Oct 17, 2018

OrthoSensor VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Left, REF ZBH-PSNCRCD39-L.
FDA Devices Moderate Oct 17, 2018

OrthoSensor VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Left, REF ZBH-PSNCRGH712-L.
FDA Devices Moderate Feb 4, 2015

Verasense Knee System, Model SYK-TRCR 02. Intelligent disposable tibial insert that measures dynamic loads during orthopedic knee surgery.

Orthosensor, Inc. holds a measurable archive slice

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

Similar medical devices volume

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

Abbott Diagnostics Scarborough, Inc. 7 Agfa N.v. 7 Alto Development Corp 7 Ambu Inc. 7

Frequently Asked Questions

How many federal recall notices name Orthosensor, Inc.? ▼
PlainRecalls indexes 7 distinct federal recall events naming Orthosensor, 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 Orthosensor, Inc. sit among other recalling firms? ▼
Orthosensor, Inc. ranks #1,996 of 14,151 by distinct recall-event count among 14,151 firms in this archive (85th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Orthosensor, Inc.'s notices? ▼
FDA Devices accounts for 7 of this firm's 7 indexed notices.
What product category dominates Orthosensor, Inc.'s filing book? ▼
Filings for Orthosensor, 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.
Orthosensor, Inc.: 7 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 Orthosensor, Inc.; individual notices remain authoritative on each linked recall page.

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