---
title: "Zeiss Intrabeam Spherical Applicator 1.5 cm REF:304534-6000-557 — FDA record Z-2649-2026 | Is It on Recall"
description: "Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications."
url: https://isitonrecall.com/recall/fda-device-z-2649-2026-zeiss-intrabeam-spherical-applicator-1-5-cm-ref-304534-6000-557/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Zeiss Intrabeam Spherical Applicator 1.5 cm REF:304534-6000-557 — FDA record Z-2649-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jun 1, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Zeiss Intrabeam Spherical Applicator 1.5 cm REF:304534-6000-557
- **Reason**: Spherical applicators (radiation therapy accessory) failed to meet manufacturing specifications.
- **Classification**: Class II
- **Recalling firm**: Carl Zeiss Meditec AG
- **Quantity**: 13 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2649-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2649-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | 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 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide - US Nationwide distribution in the state and territories of Florida and Puerto Rico. The countries of China, Germany, Ecuador, Spain, France, Malaysia, Philippines, Poland, and Romania.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Jul 8, 2026
- **Recall initiation date**: Jun 1, 2026
- **Center classification date**: Jul 1, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2649-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Carl Zeiss Meditec AG records](https://isitonrecall.com/brand/carl-zeiss-meditec-ag/)
