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Carl Zeiss Meditec Ag Recalls

7 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Carl Zeiss Meditec Ag.

7Total Recalls
0Critical
3,863Units Affected
Mar 16, 2022Most Recent
All Recalls

Every Carl Zeiss Meditec Ag Recall

Sorted by most recent. Click any recall for full details.

7 recalls
High RiskFDA
Carl Zeiss Meditec Ag
ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.
Medical Devices·1,225 affected·Mar 16, 2022
High RiskFDA
Carl Zeiss Meditec Ag
IOLMaster 700
Medical Devices·613 affected·Dec 7, 2020
High RiskFDA
Carl Zeiss Meditec Ag
Carl Zeiss Meditec AG VISUREF150 REF 2227-967 - Product Usage: is a diagnostic instrument used to determine the objective refractive valu...
Diagnostic Devices·132 affected·Aug 6, 2020
High RiskFDA
Carl Zeiss Meditec Ag
Carl Zeiss Meditec AG, Goeschwitzer Strasse 51-52 07745 Jena, Germany, IOLMaster 700, REF 1932-169 SN 1185393 2017-09-01
Medical Devices·1 affected·Jun 25, 2018
High RiskFDA
Carl Zeiss Meditec Ag
Carl Zeiss INTRABEAM PRS 500, product #304534-0000-500. The firm name on the label is Carl Zeiss Meditec AG, Jena, Germany. The INTRABE...
Medical Devices·9 affected·Aug 30, 2017
High RiskFDA
Carl Zeiss Meditec Ag
IOL Master 500: Software versions 7.5 and 7.7; Ophthalmic: IOL Master 500 is intended for biometric determination of ocular measuremen...
Medical Devices·1,882 affected·Oct 27, 2015
High RiskFDA
Carl Zeiss Meditec Ag
Treatment packs used on the VisuMax Laser Keratome. Size M Manufactured by Carl Zeiss Meditec AG, Jena, Germany. The VisuMax Lase...
Medical Devices·1 affected·Feb 3, 2014