Medical DeviceAug 26, 2026
Veritas Standard Glenoid Baseplate recall — FDA Z-2987-2026
Due to incorrect machining of peripheral screw hole resulting in potential for improper engagement of the peripheral screws.
Class IIFDA: Ongoingrestor3d Inc.
Recall history in this database
Classification mix: Class II: 4.
Medical DeviceMay 11, 2022
restor3d Evans Wedge Disposable Trials, Medium Footprint, 10mm Thickness (6101-20181018) recall — FDA Z-1027-2022
During re-work of disposable instruments to relabel for 4-year shelf-life of disposable instruments, parts got mixed into other lots.
Class IIFDA: Terminatedrestor3d Inc.
Medical DeviceMay 11, 2022
restor3d Non-Sterile Double Ended Trial Kit, Small Footprint, (6110-N01-KTS01) for the recall — FDA Z-1026-2022
Product labeled incorrectly. The lot was labeled with Small footprint when the product was Medium.
Class IIFDA: Terminatedrestor3d Inc.
Medical DeviceMay 11, 2022
restor3d Evans Wedge Disposable Trials, Large Footprint, 8mm Thickness recall — FDA Z-1028-2022
During re-work of disposable instruments to relabel for 4-year shelf-life of disposable instruments, parts got mixed into other lots.
Class IIFDA: Terminatedrestor3d Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies restor3d Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.