PlainRecalls

Omni Life Science

Compiled from official public sources by the publisher.

8 recalls on record · Latest: Nov 24, 2021

Subscribe to new Omni Life Science recalls (RSS)

Agency notice ledger

Federal filing book Omni Life Science LIGHT-BOOK · SINGLE-AGENCY

#1,784 of 14,151 · 8 notices · 0.008% archive

  • BOOK 8 notices
  • RANK #1,784 of 14,151
  • SHARE 0.008% archive
  • AGENCY FDA Devices (8)
  • CAT medical devices
  • CATS 1 category
  • LATEST Nov 24, 2021
  • PHOTO Acumedia Manufacturer…

Nearest notice-volume peer: Acumedia Manufacturers, Inc. (0 notice gap)

Omni Life Science accounts for about 0.008% of the 104,423-notice archive on 8 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 →

Omni Life Science's standing among 14,151 recalling firms

Omni Life Science ranks 1,784th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Omni Life Science vs all firms by recall-notice count

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

8 1784th of 14151 higher than 12,296 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

Omni Life Science in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Omni Life Science holds about 0.008% of archive notices alongside 8 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Nov 24, 2021

OMNI K2 Hip Stem, Manufacturer's Product Code 130006 The OMNI K2 Hip Stem is intended for use as the femoral component of a primary total hip replacement. This femoral hip stem is intended for uncemented fixation and single use implantation.
FDA Devices Low Nov 23, 2016

OMNIBotics Tracker Kit -Model: RM-10000 The TOTAL KNEE SURGETICS Navigation System with iBlock (Now OMNIBotics) is intended for use during stereotaxic surgery to aid the surgeon in locating anatomical structures and aligning the endoprostheses with the anatomical structures. It is specifically indicated for: Total Knee Arthroplasty
FDA Devices Moderate Sep 19, 2012

Omnilife Science Apex Knee System Modular Tibia Augment, Size 5 x 4mm Ref: KC-54050. The Apex Knee System is intended for use as a primary or revision total knee replacement.
FDA Devices Moderate Sep 19, 2012

Omnilife Science Apex Knee System Modular Tibia Augment, Size 4 x 4mm Ref: KC-54040. The Apex Knee System is intended for use as a primary or revision total knee replacement.
FDA Devices Moderate Sep 19, 2012

Omnilife Science Apex Knee System Modular Tibia Augment, Size 2 x 4mm Ref: KC-54020. The Apex Knee System is intended for use as a primary or revision total knee replacement.
FDA Devices Moderate Sep 19, 2012

Omnilife Science Apex Knee System Modular Tibia Augment, Size 3 x 4mm Ref: KC-54030. The Apex Knee System is intended for use as a primary or revision total knee replacement.
FDA Devices Moderate Sep 19, 2012

Omnilife Science Apex Knee System Modular Tibia Augment, Size 1 x 4mm Ref: KC-54010. The Apex Knee System is intended for use as a primary or revision total knee replacement.
FDA Devices Moderate Sep 19, 2012

Omnilife Science Apex Knee System Modular Tibia Augment, Size 6 x 4mm Ref: KC-54060. The Apex Knee System is intended for use as a primary or revision total knee replacement.

Omni Life Science 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.

Acumedia Manufacturers, Inc. 8 Adept Medical Ltd 8 Aju Pharm Co., Ltd. 8 Asante Solutions, Inc. 8

Frequently Asked Questions

How many federal recall notices name Omni Life Science? ▼
PlainRecalls indexes 8 distinct federal recall events naming Omni Life Science, 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 Omni Life Science sit among other recalling firms? ▼
Omni Life Science ranks #1,784 of 14,151 by distinct recall-event count among 14,151 firms in this archive (87th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Omni Life Science's notices? ▼
FDA Devices accounts for 8 of this firm's 8 indexed notices.
What product category dominates Omni Life Science's filing book? ▼
Filings for Omni Life Science 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.
Omni Life Science: 8 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 Omni Life Science; individual notices remain authoritative on each linked recall page.

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