RecallRadar

FDA Device recall Z-2925-2020

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)

On 2020-09-09 the FDA classified a Class II recall of 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) by Brainlab Ag, citing holding force of the Positioning Arm can be reduced by prolonged non-use.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2925-2020
ClassificationClass II
Statusterminated
Initiated2020-08-20
Published2020-09-09
Last updated2026-09-13 11:55 UTC
CompanyBrainlab Ag
DistributionDC, IL, OH

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

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

Identifiers

code_info
Article Number: 56000-01B, Description: CIRQ ARM SYSTEM 1.3.2, Serial numbers: 20100132017 20100132019 201001320…Article Number: 56000-01B, Description: CIRQ ARM SYSTEM 1.3.2, Serial numbers: 20100132017 20100132019 20100132020 20100132022 20100132023 20100132026 20100132028 20100132030 20100132031 20100132033 20100132035 20100132036 20100132037 20100132038 20100132039 Article Number: 56000-01C, Description:CIRQ ARM SYSTEM 1.4, Serial numbers: 20100140052 20100140053 20100140054 20100140055 20100140056 20100140057

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2925-2020%22

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