Zeiss Intrabeam Spherical Applicator 1 recall — Carl Zeiss Meditec AG
Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications.
Official ID Z-2649-2026 · Official record ↗
Recall found. Carl Zeiss Meditec AG is named in FDA Class II recall Z-2649-2026 covering Zeiss Intrabeam Spherical Applicator 1. Hazard: Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications. Identifying details: UDI: (01)04049539101563 Batch no: A0002 Serial numbers: US - A63141, A63086 OUS (Outside the US) - A63085, A63096, A63101, A63102, A63105, A63107, A63108, A63109, A63110, A63112, A6313. Status: Ongoing.
Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications.
Official ID Z-2649-2026 · Official record ↗
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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.