DeRoyal TRACECART POSTEROR LUMBAR FUSION TRACECART, REF 53-1961.02
Reported: December 21, 2022 Initiated: November 3, 2022 #Z-0707-2023
Product Description
DeRoyal TRACECART POSTEROR LUMBAR FUSION TRACECART, REF 53-1961.02
Reason for Recall
XXX
Details
- Recalling Firm
- DeRoyal Industries Inc
- Units Affected
- 336 kits
- Distribution
- US: Tennessee, Texas, New York, Wisconsin, Florida, Virginia, Massachusetts, Arizona, Missouri, Connecticut, New Jersey, Pennsylvania, North Carolina, Louisiana, Michigan, Minnesota, Ohio, Indiana, Kansas, Illinois, Alabama, Georgia, Mississippi
- Location
- Powell, TN
Frequently Asked Questions
What product was recalled? ▼
DeRoyal TRACECART POSTEROR LUMBAR FUSION TRACECART, REF 53-1961.02. Recalled by DeRoyal Industries Inc. Units affected: 336 kits.
Why was this product recalled? ▼
XXX
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 21, 2022. Severity: Moderate. Recall number: Z-0707-2023.
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