Cirq Arm System 2 — Class II medical device recall Z-1292-2023
Ongoing recall by Brainlab AG, reported 2023-04-05, distributed in TX. Risk of mechanical instability due to potential manufacturing error of the device
| Recall number | Z-1292-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Brainlab AG, Munich, N/A, Germany |
| Recall initiated | 2023-03-02 |
| Classified | 2023-03-28 |
| Reported by FDA | 2023-04-05 |
| Distributed | TX |
| Quantity | 1 units |
| UPC / GTIN / UDI-DI | 04056481143961 |
Product
Cirq Arm System 2.0
Reason for recall
Risk of mechanical instability due to potential manufacturing error of the device
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1292-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.