Carl Zeiss Meditec recalls
3 official recalls and safety alerts involving Carl Zeiss Meditec since 2022-03, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Carl Zeiss Meditec or the relevant agency.
- 2026-07-08
USCarl Zeiss Meditec AG recalls Zeiss Intrabeam Spherical Applicator 1.5 cm REF:304534-6000-557
Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications.
FDA · DeviceCarl Zeiss Meditec AGWorldwide - US Nationwide distribution in the state and territories of Florida…Official notice →- 2022-05-04
- US
Carl Zeiss Meditec AG recalls ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.
High friction of the slider can cause the device to stick, or not move as intended.
FDA · DeviceCarl Zeiss Meditec AGU.S.: AL, AR, AZ, CA, CT, FL, GA, IA, IL, KS, LA, MA, MD, MI, MN, MO, MS, MT,…Official notice → - 2022-03-16
- US
Carl Zeiss Meditec, Inc. recalls CIRRUS HD-OCT, Models 5000 AngioPlex and 6000 AngioPlex
Optic nerve head angiography scan to be turned off due to its distribution without pre-market clearance.
FDA · DeviceCarl Zeiss Meditec, Inc.U.S Nationwide Distribution.: OH, CA, IN, AR, IA, LA, WI, OK, IL, OR, AL, KY,…Official notice →