FDA Enforcement Class II Terminated

Carousel MAS1025-01, part of the Brain Surgical Accessories Intra-operative Kit (KIT0295), accessory used with the Renaissance System (TPL0038). Indicated for precise positioning of surgical instruments or spinal implants during general spinal and brain surgery. It is intended to be used whenever the clinician and/or patient benefits from generated 3D imaging of, high contrast objects.

Recall: Z-0609-2019 · Reported December 26, 2018

Enforcement

Recall Number
Z-0609-2019
Event ID
81521
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Mazor Robotics Ltd
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
December 26, 2018
Initiation Date
November 26, 2014
Classification Date
December 14, 2018
Termination Date
July 3, 2019
Address
5 Shacham Street, P.O. Box 3104, North Industrial Park, N/A, Israel

Description

Carousel MAS1025-01, part of the Brain Surgical Accessories Intra-operative Kit (KIT0295), accessory used with the Renaissance System (TPL0038). Indicated for precise positioning of surgical instruments or spinal implants during general spinal and brain surgery. It is intended to be used whenever the clinician and/or patient benefits from generated 3D imaging of, high contrast objects.

Reason

In some situations the carousel position pin (locker) may cause the carousel upper plate to pop out and the carousel may then inadvertently move.

Code Info

Affected products: all Carousels under Level 01 were affected and therefore are applicable to this issue. The related lots include: WP065611, WP066389, WP066411, WP066412, WP066420. Explanation of the coding system: a part number (e.g. MAS1025-01) is composed of a generic part number related to the part (e.g. MAS1025) and the level of the part (e.g. 01).

Distribution

Affected devices were distributed in the US to four different medical facilities in four states

Quantity

5 units