Cirq Arm System — Class II medical device recall Z-2925-2020
Terminated recall by Brainlab AG, reported 2020-09-09, distributed in DC, IL, OH. Holding force of the Positioning Arm can be reduced by prolonged non-use.
| Recall number | Z-2925-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Brainlab AG, Munich, N/A, Germany |
| Recall initiated | 2020-08-20 |
| Classified | 2020-08-29 |
| Reported by FDA | 2020-09-09 |
| Terminated | 2021-05-13 |
| Distributed | DC, IL, OH |
| Countries outside the US | BG, DE, FR, GB |
| Quantity | 21 arms |
| Serial numbers | 20100132017, 20100132019, 20100132020, 20100132022, 20100132023, 20100132026, 20100132028, 20100132030, 20100132031, 20100132033, 20100132035, 20100132036, 20100132037, 20100132038, 20100132039, 20100140052, 20100140053, 20100140054, 20100140055, 20100140056, 20100140057 |
| Model numbers | 1.3.2 |
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.
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-2925-2020. 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.