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Carl Zeiss Meditec AG FDA Recalls
2 recalls on file across devices, 0 of them Class I and 2 still open. Matched by name to CZMWY.
Newest first
Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.
| Product |
|---|
| Zeiss Intrabeam Spherical Applicator 1.5 cm REF:304534-6000-557Class IIJun 1, 2026Spherical applicators (radiation therapy accessory) failed t |
| ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.Class IIMar 16, 2022High friction of the slider can cause the device to stick, o |