FDA Class II Medical Devices

restor3d Inc.: Brand Name: Veritas Standard Reverse Total Shoulder Product Name: Veritas Standard Glenoid Baseplate Model/Catalog Number: 1500-1030; 1500-1035…

restor3d Inc. · Affected quantity: 59

Hazard
Due to incorrect machining of peripheral screw hole resulting in potential for improper engagement of the peripheral screws.

Details
Distribution: U.S. Nationwide distribution in the state of Texas.. Recall #Z-2987-2026, initiated 20260630. Voluntary: Firm initiated.

Products affected
Brand Name: Veritas Standard Reverse Total Shoulder Product Name: Veritas Standard Glenoid Baseplate Model/Catalog Number: 1500-1030; 1500-1035 Software Version: N/A - off-the-shelf hardware product Product Description: The restor3d Reverse Total Shoulder Arthroplasty System is intended for patient…

Recall status
Ongoing

Reference: FDA Z-2987-2026 · Issued August 26, 2026 · Class II · Indexed by RecallSweep from the official FDA feed.

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