PlainRecalls

Carl Zeiss Meditec, Inc.

Compiled from official public sources by the publisher.

10 recalls on record · Latest: Mar 16, 2022

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Agency notice ledger

Federal filing book Carl Zeiss Meditec, Inc. LIGHT-BOOK · SINGLE-AGENCY

#1,440 of 14,151 · 10 notices · 0.010% archive

  • BOOK 10 notices
  • RANK #1,440 of 14,151
  • SHARE 0.010% archive
  • AGENCY FDA Devices (10)
  • CAT medical devices
  • CATS 1 category
  • LATEST Mar 16, 2022
  • PHOTO 4e Brands North Ameri…

Nearest notice-volume peer: 4e Brands North America, Llc (0 notice gap)

Carl Zeiss Meditec, Inc. accounts for about 0.010% of the 104,423-notice archive on 10 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 Carl Zeiss Meditec, Inc. compares to 14,151 recalling firms

Carl Zeiss Meditec, Inc. ranks 1,440th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Carl Zeiss Meditec, Inc. vs all firms by recall-notice count

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

10 1440th of 14151 higher than 12,602 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

Carl Zeiss Meditec, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Carl Zeiss Meditec, Inc. holds about 0.010% of archive notices alongside 10 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Mar 16, 2022

CIRRUS HD-OCT, Models 5000 AngioPlex and 6000 AngioPlex
FDA Devices Moderate Aug 18, 2021

Chassis Label - "CIRRUS HD-OCT Rx-Only" Product Label Exterior RX - "CIRRUS HD-OCT Model 6000"
FDA Devices Moderate Jan 8, 2020

The PLEX Elite 9000, a Swept-Source OCT [SS-OCT] - Product Usage: The PLEX Elite 9000 Swept-Source OCT [SS-OCT] is a non- contact, high resolution, wide field of view tomographic and biomicroscopic imaging device intended for in-vivo viewing, axial cross-sectional and three-dimensional imaging of posterior ocular structures. The device is indicated for visualizing posterior ocular structures including, but not limited to, retina, retinal nerve fiber layer, ganglion cell plus inner plexiform lay
FDA Devices Moderate Dec 25, 2019

VisuMax Software Version 2.10.13 with activated Software-Module ReLEx (SMILE) option used in conjunction with the VisuMax Femtosecond Laser System for Refractive Correction. Catalog Number 0000000-1345-518 Product Usage: The VisuMax Femtosecond Laser is a precision ophthalmic surgical laser designed for the creation of incisions in the cornea. The VisuMax Femtosecond Laser is indicated for use in small incision lenticule extraction (SMILE) for the reduction or elimination of myopia. This d
FDA Devices Moderate Nov 27, 2013

Zeiss brand IOLMaster 500, Model 500, Biomicroscope, Slit-Lamp, AC-Powered, Product is manufactured by Carl Zeiss Meditec AG (Jena), Carl Zeiss Promenade 10, Jena, Germany 07745; and distributed by Carl Zeiss Meditec, Inc., Dublin, CA This device is intended for use primarily by physicians and health care workers and may be only used under the supervision of a physician. This device will not be sold to the general public. The IOLMaster is intended for the biometric determination of ocula
FDA Devices Moderate Nov 27, 2013

Zeiss brand IOLMaster, Version 1-5, Biomicroscope, Slit-Lamp, AC-Powered, Product is manufactured by Carl Zeiss Meditec AG (Jena), Carl Zeiss Promenade 10, Jena, Germany 07745; and distributed by Carl Zeiss Meditec, Inc., Dublin, CA This device is intended for use primarily by physicians and health care workers and may be only used under the supervision of a physician. This device will not be sold to the general public. The IOLMaster is intended for the biometric determination of ocular

FDA Devices Moderate Jun 12, 2013

Zeiss brand OPMI Pentero C, Surgical microscope and accessories, Model: OPMI Pentero C, Product Numbers: 302583-9001-000 (PENTERO C), and 305961-0000-00 (Ceiling Mount for PENTERO C), Product Usage: A surgical microscope and accessories is an AC-powered device intended for use during surgery to provide a magnified view of the surgical field.
FDA Devices Moderate Nov 28, 2012

INTRABEAM Balloon Applicator Set; 3.5 cm, Carl Zeiss Meditec AG, Oberkochen, Germany INTRABEAM System is intended for radiation therapy treatments.
FDA Devices Moderate Nov 28, 2012

INTRABEAM Balloon Applicator Set; 3.0 cm, Carl Zeiss Meditec AG, Oberkochen, Germany INTRABEAM System is intended for radiation therapy treatments
FDA Devices Moderate Nov 28, 2012

INTRABEAM Balloon Applicator Set; 4.0 cm, Carl Zeiss Meditec AG, Oberkochen, Germany INTRABEAM System is intended for radiation therapy treatments.

Carl Zeiss Meditec, 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.

Amerx Health Care Corp. 10 Bausch & Lomb Surgical, Inc. 10 Beekley Corporation 10 Cypress Medical Products LLC 10

Frequently Asked Questions

How many federal recall notices name Carl Zeiss Meditec, Inc.? ▼
PlainRecalls indexes 10 distinct federal recall events naming Carl Zeiss Meditec, 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 Carl Zeiss Meditec, Inc. sit among other recalling firms? ▼
Carl Zeiss Meditec, Inc. ranks #1,440 of 14,151 by distinct recall-event count among 14,151 firms in this archive (89th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Carl Zeiss Meditec, Inc.'s notices? ▼
FDA Devices accounts for 10 of this firm's 10 indexed notices.
What product category dominates Carl Zeiss Meditec, Inc.'s filing book? ▼
Filings for Carl Zeiss Meditec, 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.
Carl Zeiss Meditec, Inc.: 10 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 Carl Zeiss Meditec, Inc.; individual notices remain authoritative on each linked recall page.

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