Stryker Howmedica Osteonics recalls

Stryker Howmedica Osteonics has 86 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 31 May 2017. 2 are still ongoing. The most frequent reason is sterility.

Total recalls86since 2012

Last 12 months0reported

Class I11% of total

Ongoing2latest 31 May 2017

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 1 1%Class II 85 99%Class III 0 0%

Why stryker howmedica osteonics is recalled

Product types

By year

201722%
20163035%
20152023%
201489%
20131416%
20121214%

Ongoing stryker howmedica osteonics recalls

2 active

Reported	Class	Recall	Company	Reason	Where
1 Aug 2012Device	CLASS II	Rejuvenate Modular Stems Stryker Ireland Carrigtwohill recalled	Stryker Howmedica Osteonics	Other	Nationwide
1 Aug 2012Device	CLASS II	ABG II Modular Hip Stem Stryker Howmedica Osteonics Corp recalled	Stryker Howmedica Osteonics	Other	Nationwide

All stryker howmedica osteonics recalls, newest first

86 total

Reported	Class	Recall	Company	Reason	Where
31 May 2017Device	CLASS II	Hoffmann LRF Safety Clip (Bone Transport Strut) recalled	Stryker Howmedica Osteonics	Other	Nationwide
18 Jan 2017Device	CLASS II	Reunion TSA Peg Alignment Sound recalled by Stryker Howmedica Osteonics	Stryker Howmedica Osteonics	Other	Nationwide
28 Dec 2016Device	CLASS II	GAM Kirschner Wire, Sterile R, T2 K-Wire, Sterile R recalled	Stryker Howmedica Osteonics	Sterility	Nationwide
16 Nov 2016Device	CLASS II	LFIT Anatomic V40 Femoral Head, Low Friction Ion Treatment, Sterile recalled	Stryker Howmedica Osteonics	Sterility	Nationwide
19 Oct 2016Device	CLASS II	Stryker Orthopaedics Universal Acetabular Cup Positioner/Impactor recalled	Stryker Howmedica Osteonics	Sterility	Nationwide
21 Sep 2016Device	CLASS II	Stryker Orthopaedics Patella Assembly Instrument recalled	Stryker Howmedica Osteonics	Sterility	Nationwide
21 Sep 2016Device	CLASS II	Femoral Nail, A/R T2 Femur mm T2 Femoral Nailing System is recalled	Stryker Howmedica Osteonics	Labeling Errors	CA
21 Sep 2016Device	CLASS II	Supracondylar Nail T2 SCN mm T2 Supracondylar Nail System recalled	Stryker Howmedica Osteonics	Labeling Errors	CA
17 Aug 2016Device	CLASS II	Stryker Orthopaedics Modular Handle Triathlon Instruments recalled	Stryker Howmedica Osteonics	Sterility	Nationwide
17 Aug 2016Device	CLASS II	Orthopedic manual surgical instrument Usage recalled	Stryker Howmedica Osteonics	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.