FDA Device recall Z-1292-2023
Cirq Arm System 2.0
- FDA Device
- Class II
- ongoing
- Published 2023-04-05
On 2023-04-05 the FDA classified a Class II recall of Cirq Arm System 2.0 by Brainlab Ag, citing risk of mechanical instability due to potential manufacturing error of the device.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1292-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-03-02 |
| Published | 2023-04-05 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Brainlab Ag |
| Distribution | TX |
Product
Cirq Arm System 2.0
Reason
Risk of mechanical instability due to potential manufacturing error of the device
Identifiers
| code_info | 56500 CIRQ ARM SYSTEM 2.0; GTIN 04056481143961; All available Serial numbers/lot numbers are affected. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1292-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.