Orthosensor recalls

Orthosensor has 8 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 17 Oct 2018. The most frequent reason is device malfunction.

Total recalls8since 2012

Last 12 months0reported

Class I00% of total

Ongoing0latest 17 Oct 2018

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 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 8 100%Class III 0 0%

Why orthosensor is recalled

Device Malfunction788%
Foreign Material113%

Product types

Other Medical Devices675%
Hip & Knee Implants225%

By year

2018675%
2015113%
2012113%

All orthosensor recalls, newest first

8 total

Reported	Class	Recall	Company	Reason	Where
17 Oct 2018Device	CLASS II	Verasense for Zimmer Biomet Persona CR G-H/7-12 Left recalled	Orthosensor	Device Malfunction	7 states
17 Oct 2018Device	CLASS II	Verasense for Zimmer Biomet Persona CR C-D/3-9 Left recalled	Orthosensor	Device Malfunction	7 states
17 Oct 2018Device	CLASS II	Verasense for Zimmer Biomet Persona CR C-D/3-9 Right recalled	Orthosensor	Device Malfunction	7 states
17 Oct 2018Device	CLASS II	Verasense for Zimmer Biomet Persona CR E-F/3-11 Right recalled	Orthosensor	Device Malfunction	7 states
17 Oct 2018Device	CLASS II	Verasense for Zimmer Biomet Persona CR G-H/7-12 Right recalled	Orthosensor	Device Malfunction	7 states
17 Oct 2018Device	CLASS II	Verasense for Zimmer Biomet Persona CR E-F/3-11 Left recalled	Orthosensor	Device Malfunction	7 states
4 Feb 2015Device	CLASS II	Verasense Knee System recalled by Orthosensor	Orthosensor	Device Malfunction	6 states
31 Oct 2012Device	CLASS II	"**Ortho Sensor12-123-A Knee Trial recalled	Orthosensor	Foreign Material	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.