Stryker Craniomaxillofacial Division recalls

Stryker Craniomaxillofacial Division has 6 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 14 Oct 2015. The most frequent reason is potency & assay.

Total recalls6since 2013

Last 12 months0reported

Class I00% of total

Ongoing0latest 14 Oct 2015

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 6 100%Class III 0 0%

Why stryker craniomaxillofacial division is recalled

Product types

Surgical Instruments583%
Hip & Knee Implants117%

By year

2015583%
2013117%

All stryker craniomaxillofacial division recalls, newest first

6 total

Reported	Class	Recall	Company	Reason	Where
14 Oct 2015Device	CLASS II	Disposable Paper, Medical Accessory, 100 DISP, Paper F recalled	Stryker Craniomaxillofacial Division	Sterility	MI
18 Feb 2015Device	CLASS II	Medpor Titan Max Orbital Floor and Wall recalled	Stryker Craniomaxillofacial Division	Other	Nationwide
18 Feb 2015Device	CLASS II	Medpor Surgical Implant Contoured Two Piece Chin recalled	Stryker Craniomaxillofacial Division	Device Malfunction	Nationwide
18 Feb 2015Device	CLASS II	Medpor Barrier Sheets Orbital Floor Implant recalled	Stryker Craniomaxillofacial Division	Potency & Assay	Nationwide
18 Feb 2015Device	CLASS II	Medpor Barrier Sheets Rectangle recalled by Stryker Craniomaxillofacial	Stryker Craniomaxillofacial Division	Potency & Assay	Nationwide
4 Sep 2013Device	CLASS II	Stryker Part Numbers 79-43903 (3cc), 79-43905 (5cc) recalled	Stryker Craniomaxillofacial Division	Lead & Heavy Metals	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.