ClearanceBrief
Recall Z-2428-2015 ยท JDB Prosthesis, Elbow, Semi-Constrained, Cemented

Stryker Howmedica Osteonics Corp.

Radio-Capitellum, Capitellum, Left, Large, Do Not Reuse, Rx Only. Indicated for use in the elbow for reduction or relief of pain and/or improved elbow function in skeletally mature patients.

DateAug 20, 2015 (initiated Jun 24, 2015)
StatusTerminated
ReasonStryker is recalling rHead, uHead, Sigmoid Notch, Remotion, Radio Capitellum because packaging integrity (sterile barrier) of the packaging type KIT I may potentially be compromised by transportation.
Root causePackaging change control
ActionBranches/Agencies were notified by Stryker of this action by e-mails on June 24, 2015 and an Urgent Medical Device Removal Letter/Acknowledgement Response Form dated June 25, 2015 was sent to the attention of the Risk Manager.
Quantity16992 total
DistributionWorldwide Distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K070236SBI LATERAL RADIO CAPITELLUM
Small Bone Innovations, Inc., Feb 21, 2007