Orthoscan recalls

Orthoscan has 11 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 11 Dec 2024. 7 are still ongoing. The most frequent reason is device malfunction.

Total recalls11since 2018

Last 12 months0reported

Class I00% of total

Ongoing7latest 11 Dec 2024

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 7 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 11 100%Class III 0 0%

Why orthoscan is recalled

Device Malfunction11100%

Product types

By year

2024764%
2018436%

Ongoing orthoscan recalls

7 active

Reported	Class	Recall	Company	Reason	Where
11 Dec 2024Device	CLASS II	Ziehm Vision FD recalled by Orthoscan	Orthoscan	Device Malfunction	PR
11 Dec 2024Device	CLASS II	Ziehm Vision RFD 3D recalled by Orthoscan	Orthoscan	Device Malfunction	PR
11 Dec 2024Device	CLASS II	Ziehm Vision R recalled by Orthoscan	Orthoscan	Device Malfunction	PR
11 Dec 2024Device	CLASS II	Ziehm Vision system, x-ray, tomography, computed recalled by Orthoscan	Orthoscan	Device Malfunction	PR
11 Dec 2024Device	CLASS II	Ziehm Vision RFD recalled by Orthoscan	Orthoscan	Device Malfunction	PR
11 Dec 2024Device	CLASS II	Ziehm Solo FD recalled by Orthoscan	Orthoscan	Device Malfunction	PR

All orthoscan recalls, newest first

11 total

Reported	Class	Recall	Company	Reason	Where
11 Dec 2024Device	CLASS II	Ziehm Vision FD recalled by Orthoscan	Orthoscan	Device Malfunction	PR
11 Dec 2024Device	CLASS II	Ziehm Vision RFD 3D recalled by Orthoscan	Orthoscan	Device Malfunction	PR
11 Dec 2024Device	CLASS II	Ziehm Vision R recalled by Orthoscan	Orthoscan	Device Malfunction	PR
11 Dec 2024Device	CLASS II	Ziehm Vision system, x-ray, tomography, computed recalled by Orthoscan	Orthoscan	Device Malfunction	PR
11 Dec 2024Device	CLASS II	Ziehm Vision RFD recalled by Orthoscan	Orthoscan	Device Malfunction	PR
11 Dec 2024Device	CLASS II	Ziehm Solo FD recalled by Orthoscan	Orthoscan	Device Malfunction	PR
11 Dec 2024Device	CLASS II	Ziehm Solo. Digital Mobile C-arm recalled by Orthoscan	Orthoscan	Device Malfunction	PR
17 Jan 2018Device	CLASS II	Mobile Mini C-arm system Part # recalled by Orthoscan	Orthoscan	Device Malfunction	Nationwide
17 Jan 2018Device	CLASS II	Mobile Mini C-arm system Part # recalled by Orthoscan	Orthoscan	Device Malfunction	Nationwide
17 Jan 2018Device	CLASS II	Mobile Mini C-arm system Part # 1000-0004-FD recalled by Orthoscan	Orthoscan	Device Malfunction	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.