Concorde Lift Driver Shaft AO. Used with supplemental internal spinal fixation systems that have been cleared for use in the lumbar spine.
Reported: March 14, 2018 Initiated: July 26, 2017 #Z-0848-2018
Product Description
Concorde Lift Driver Shaft AO. Used with supplemental internal spinal fixation systems that have been cleared for use in the lumbar spine.
Reason for Recall
Potential for Intra-operative breakage of driver tips
Details
- Recalling Firm
- DePuy Orthopaedics, Inc.
- Units Affected
- 130 units total
- Distribution
- Nationwide Distribution
- Location
- Raynham, MA
Frequently Asked Questions
What product was recalled? ▼
Concorde Lift Driver Shaft AO. Used with supplemental internal spinal fixation systems that have been cleared for use in the lumbar spine.. Recalled by DePuy Orthopaedics, Inc.. Units affected: 130 units total.
Why was this product recalled? ▼
Potential for Intra-operative breakage of driver tips
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 14, 2018. Severity: Moderate. Recall number: Z-0848-2018.
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