FDAClass IIApril 5, 2023

Cirq Arm System 2.0 recall

Cirq Arm System 2.0

Why was Cirq Arm System 2.0 recalled?

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

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

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

Product
Cirq Arm System 2.0
Recalling firm
Brainlab AG
Quantity
1 unit
Distribution
Texas
Recall date
April 5, 2023
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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