Mazor Robotics Ltd: Mazor X robotic guidance system REF: TPL0059
Read the official notice at FDA (device) →
The text below is copied from the official FDA (device) record. If anything differs, the official notice is correct.
- Company / brand
- Mazor Robotics Ltd
- Product
- Mazor X robotic guidance system REF: TPL0059
- Reason / hazard
- Software errors that can result in incorrect surgical instrument positioning during spinal surgery.
- Classification
- Class II
- Status
- Ongoing
- Distribution / sold at
- Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belgium, Brazil, Canada, Canary Islands, China, Croatia, France, Germany, Greece, Hong Kong, Hungary, India, Israel, Italy, Japan, Malaysia, Mexico, Netherlands, Poland, Portugal, Puerto Rico, Romania, Singapore, Slovakia, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, Ukraine, United Arab Emirates, United Kingdom, United States, Vietnam.
- Recall initiated
- 2025-12-10
- Code info
- Software versions: 5.0.1, 5.1.2, 5.1.3/ UDI: 07290109180465, 07290109184524, 07290109181158, 00763000635169, 07290109183213, 07290109184517, 00763000419134, 00763000431761, 07290109184098, 07290109184838, 07290115751376, 07290115751895
- Product quantity
- 549 systems
- Voluntary mandated
- Voluntary: Firm initiated
- City
- Caesarea
- Country
- Israel
- Event id
- 98199
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