Brainlab AG: Medical Device Recall in 2023 - (Recall #: Z-1292-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Cirq Arm System 2.0

Product Classification:

Class II

Date Initiated: March 2, 2023

Date Posted: April 5, 2023

Recall Number: Z-1292-2023

Event ID: 91781

Reason for Recall:

Risk of mechanical instability due to potential manufacturing error of the device

Status: Ongoing

Product Quantity: 1 unit

Code Information:

56500 CIRQ ARM SYSTEM 2.0; GTIN 04056481143961; All available Serial numbers/lot numbers are affected.

Distribution Pattern:

Texas

Voluntary or Mandated:

Voluntary: Firm initiated