Ortho Development recalls

Ortho Development has 8 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 13 May 2020. 2 are still ongoing. The most frequent reason is packaging defects.

Total recalls8since 2014

Last 12 months0reported

Class I00% of total

Ongoing2latest 13 May 2020

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 ortho development is recalled

Product types

Hip & Knee Implants8100%

By year

2020225%
2014675%

Ongoing ortho development recalls

2 active

Reported	Class	Recall	Company	Reason	Where
13 May 2020Device	CLASS II	Tibial Tray Nonporous A Size recalled by Ortho Development	Ortho Development	Device Malfunction	6 states
13 May 2020Device	CLASS II	Tibial Tray Nonporous A Size recalled by Ortho Development	Ortho Development	Device Malfunction	6 states

All ortho development recalls, newest first

8 total

Reported	Class	Recall	Company	Reason	Where
13 May 2020Device	CLASS II	Tibial Tray Nonporous A Size recalled by Ortho Development	Ortho Development	Device Malfunction	6 states
13 May 2020Device	CLASS II	Tibial Tray Nonporous A Size recalled by Ortho Development	Ortho Development	Device Malfunction	6 states
27 Aug 2014Device	CLASS II	Patella, REF164 recalled by Ortho Development	Ortho Development	Packaging Defects	Nationwide
27 Aug 2014Device	CLASS II	Pivot Bipolar Cup /43 recalled by Ortho Development	Ortho Development	Packaging Defects	Nationwide
27 Aug 2014Device	CLASS II	PS Tibial Insert recalled by Ortho Development	Ortho Development	Packaging Defects	Nationwide
27 Aug 2014Device	CLASS II	Tibila Insert CK, Balanced Knee System Revision, REF563-1YYY recalled	Ortho Development	Packaging Defects	Nationwide
27 Aug 2014Device	CLASS II	Tibila Insert UC, Balanced Knee System, REF163-3YYY recalled	Ortho Development	Packaging Defects	Nationwide
21 May 2014Device	CLASS II	PS-C Femoral Nonporous Rt Sz recalled by Ortho Development	Ortho Development	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.