Carl Zeiss Meditec AG recalls
Every recall we track for Carl Zeiss Meditec AG — 7 in all, from 2017–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Carl Zeiss Meditec AG peaked in 2020 (3); 7 since 2017.
All FDA recall records for Carl Zeiss Meditec AG since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 1 | 0 | 1 |
| 2018 | 0 | 0 | 1 | 0 | 1 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 2 | 1 | 0 | 3 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 1 | 0 | 0 | 1 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 1 | 1 |
What to do if you have a recalled Carl Zeiss Meditec AG product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Carl Zeiss Meditec AG recalls
6 shown- UnratedMedical device
Carl Zeiss Meditec AG recalls Zeiss Intrabeam Spherical Applicator 1.5 cm REF:304534-6000-557
Carl Zeiss Meditec recalls specific Zeiss Intrabeam Spherical Applicators due to failing to meet manufacturing specifications. Affected units include certain serial numbers and batch numbers. Consumers should contact the manufacturer for details.
Carl Zeiss MeditecJun 1, 2026 - Use cautionMedical device
Carl Zeiss Meditec AG recalls ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.
ZEISS miLOOP Lens Fragmentation Device (model 303071-9090-000) used in cataract surgery may stick due to high friction. Affected units sold in 2011-2023; recall issued for safety.
Carl Zeiss MeditecMar 16, 2022 - Lower riskMedical device
Carl Zeiss Meditec AG recalls IOLMaster 700
Carl Zeiss Meditec recalls IOLMaster 700 devices with specific software versions due to potential patient data mismatch during patient list selection. Affected units may need software update or correction.
Carl Zeiss MeditecDec 7, 2020 - Use cautionMedical device
Carl Zeiss Meditec AG recalls Carl Zeiss Meditec AG VISUREF150 REF 2227-967 - Product Usage: is a diagnostic instrument used to determine the
Carl Zeiss Meditec recalls VISUREF150 eye diagnostic devices with serial numbers pending due to faulty DC/DC converter causing electrical shock risk. Affected units may have increased current leakage.
Carl Zeiss MeditecAug 6, 2020 - Lower riskMedical device
Carl Zeiss Meditec AG recalls Carl Zeiss Meditec AG, Goeschwitzer Strasse 51-52 07745 Jena, Germany, IOLMaster 700, REF 1932-169 SN 1185393 2017-09-01
Carl Zeiss Meditec recalls IOLMaster 700 devices with serial number 1185393 due to incorrect calibration causing inaccurate eye imaging. Affected units may provide wrong measurements for eye surgery planning.
Carl Zeiss MeditecJun 25, 2018 - Lower riskMedical device
Carl Zeiss Meditec AG recalls Carl Zeiss INTRABEAM PRS 500, product #304534-0000-500. The firm name on the label is Carl Zeiss Meditec AG, Jena,
Carl Zeiss Meditec recalls specific INTRABEAM PRS 500 radiation therapy devices with incorrect calibration values on certificates. Affected units may not deliver accurate radiation doses.
Carl Zeiss MeditecAug 30, 2017
Carl Zeiss Meditec AG recall questions
How many recalls has Carl Zeiss Meditec AG had?
7 recalls from Carl Zeiss Meditec AG are on record with U.S. safety agencies, from 2017–2026.
What is the most recent Carl Zeiss Meditec AG recall?
Carl Zeiss Meditec AG recalls Zeiss Intrabeam Spherical Applicator 1.5 cm REF:304534-6000-557, dated Jun 1, 2026. Every Carl Zeiss Meditec AG recall is listed on this page, newest first.
What should I do if I have a recalled Carl Zeiss Meditec AG product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Carl Zeiss Meditec AG recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.