Stryker Howmedica Osteonics Corp.: Medical Device Recall in 2013 - (Recall #: Z-0919-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Command Instrument Broach Handle. Used in Total Hip Arthroplasty. Catalog Number: 6266-0-100

Product Classification:

Class II

Date Initiated: December 20, 2012

Date Posted: March 20, 2013

Recall Number: Z-0919-2013

Event ID: 64306

Reason for Recall:

Reports of handle fracture and subsequent disassociation of cam assembly subcomponents during use.

Status: Terminated

Product Quantity: 48 units

Code Information:

Catalog Number: 6266-0-100 Lot Code: RD6W017, RD7L234X, RD7L234, RD7L235, RD5T305A, RD6W017J, RD6W017A, RD5T307, RD5T305T, RD5T305M, RD5T305L, RD5T306X, RD5T305, RD5T306

Distribution Pattern:

Nationwide Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated