restor3d recalls

restor3d has 5 recalls on record with the FDA and USDA, the earliest in 2022 and the latest reported on 23 Sep 2026. 2 are still ongoing. 2 were reported in the last 12 months.

Total recalls5since 2022

Last 12 months2reported

Class I00% of total

Ongoing2latest 23 Sep 2026

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 0 0 0May 0 0 1Aug 1 0

Severity split

Class I 0 0%Class II 5 100%Class III 0 0%

Why restor3d is recalled

Product types

Hip & Knee Implants480%
Other Medical Devices120%

By year

2026240%
2022360%

Ongoing restor3d recalls

2 active

Reported	Class	Recall	Company	Reason	Where
23 Sep 2026Device	CLASS II	Kinos Axiom Total Ankle System with Axiom PSR, Flat-cut (Cut Guide) recalled	restor3d	Packaging Defects	Nationwide
26 Aug 2026Device	CLASS II	Veritas Standard Reverse Total Shoulder Veritas Standard recalled	restor3d	Device Malfunction	Nationwide

All restor3d recalls, newest first

5 total

Reported	Class	Recall	Company	Reason	Where
23 Sep 2026Device	CLASS II	Kinos Axiom Total Ankle System with Axiom PSR, Flat-cut (Cut Guide) recalled	restor3d	Packaging Defects	Nationwide
26 Aug 2026Device	CLASS II	Veritas Standard Reverse Total Shoulder Veritas Standard recalled	restor3d	Device Malfunction	Nationwide
11 May 2022Device	CLASS II	Evans Wedge Disposable Trials, Large Footprint Thickness recalled	restor3d	Other	Nationwide
11 May 2022Device	CLASS II	Non-Sterile Double Ended Trial Kit, Small Footprint recalled by restor3d	restor3d	Other	Nationwide
11 May 2022Device	CLASS II	Evans Wedge Disposable Trials, Medium Footprint Thickness recalled	restor3d	Other	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.