# FDA recall Z-2925-2020

> **Brainlab AG** · Class II · device recall initiated 2020-08-20.

## Product

Cirq Arm System - Model SBS 1.3.2 (Art.No. 56000-01B) and SBS 1.4 (Art.No. 56000-01C) of the CIRQ Arm System (56000 and 56000A)

## Reason for recall

Holding force of the Positioning Arm can be reduced by prolonged non-use.

## Distribution

USA: DC, OH, IL    OUS: Bulgaria; France; Germany; United Kingdom

## Key facts

- **Recall number:** Z-2925-2020
- **Recalling firm:** Brainlab AG
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-08-20
- **Report date:** 2020-09-09
- **Termination date:** 2021-05-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Munich, N/A, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2925-2020

## Citation

> AI Analytics. FDA recall Z-2925-2020. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-2925-2020. Source: US FDA. Licensed CC0.

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