PlainRecalls

Oculus Optikgeraete Gmbh

Compiled from official public sources by the publisher.

7 recalls on record · Latest: Sep 6, 2023

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Agency notice ledger

Federal filing book Oculus Optikgeraete Gmbh LIGHT-BOOK · SINGLE-AGENCY

#1,995 of 14,151 · 7 notices · 0.007% archive

  • BOOK 7 notices
  • RANK #1,995 of 14,151
  • SHARE 0.007% archive
  • AGENCY FDA Devices (7)
  • CAT medical devices
  • CATS 1 category
  • LATEST Sep 6, 2023
  • PHOTO A I Foods Corporation

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

Oculus Optikgeraete Gmbh 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 →

How Oculus Optikgeraete Gmbh compares to 14,151 recalling firms

Oculus Optikgeraete Gmbh ranks 1,995th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Oculus Optikgeraete Gmbh vs all firms by recall-notice count

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

7 1995th 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

Oculus Optikgeraete Gmbh in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Oculus Optikgeraete Gmbh 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 Sep 6, 2023

Oculus Pentacam AXL , Ref 70100, CE 0123
FDA Devices Moderate Sep 6, 2023

Oculus Myopia Master , Ref 68100, CE 0123
FDA Devices Moderate Sep 6, 2023

Oculus Pentacam AXL Wave, Ref 70020, CE 0123
FDA Devices Moderate Sep 7, 2022

Pentacam AXL REF 70100, Pentacam HR REF 70900. Used to image the anterior segment of the eye.
FDA Devices Moderate Sep 7, 2022

Pentacam AXL Wave REF 70020. Used to image the anterior segment of the eye.
FDA Devices Moderate Sep 7, 2022

Pentacam HR REF 70900. Used to image the anterior segment of the eye.
FDA Devices Moderate Feb 28, 2018

OCULUS Pentacam AXL, Model 70100, software versions 1.21r01, 1.21r03, 1.21r11, and 1.21r13. The firm name on the label is OCULUS Optikgerate GmbH, Made in Germany. The Pentacam AXL is designed to take photos of the anterior segment of the eye, which includes the cornea, pupil, anterior chamber, and lens of the eye, to evaluate corneal shape, analyze condition of the lens (opaque crystalline lens), analyze the anterior chamber angle, analyze anterior chamber depth, analyze the volume of the a

Oculus Optikgeraete Gmbh 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 Alto Development Corp 7 Ambu Inc. 7 Andover Healthcare Inc. 7

Frequently Asked Questions

How many federal recall notices name Oculus Optikgeraete Gmbh? ▼
PlainRecalls indexes 7 distinct federal recall events naming Oculus Optikgeraete Gmbh, 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 Oculus Optikgeraete Gmbh sit among other recalling firms? ▼
Oculus Optikgeraete Gmbh ranks #1,995 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 Oculus Optikgeraete Gmbh's notices? ▼
FDA Devices accounts for 7 of this firm's 7 indexed notices.
What product category dominates Oculus Optikgeraete Gmbh's filing book? ▼
Filings for Oculus Optikgeraete Gmbh 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.
Oculus Optikgeraete Gmbh: 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 Oculus Optikgeraete Gmbh; individual notices remain authoritative on each linked recall page.

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