Stryker Howmedica Osteonics Corp.: Medical Device Recall in 2013 - (Recall #: Z-2099-2013)

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:

Stryker 1) Asnis III Cannulated Screw REF 604640 4.0x40mm TL 13.5mm 2) Asnis III Cannulated Screw REF 604642S 4.0x42mm TL 14mm, sterile Product Usage: The Asnis III Cannulated Screw System is intended for fracture fixation of small and long bones and of the pelvis. The system is not intended for spinal use.

Product Classification:

Class II

Date Initiated: July 8, 2013

Date Posted: September 4, 2013

Recall Number: Z-2099-2013

Event ID: 65891

Reason for Recall:

Stryker received a report that the length of the cannulated screw asnis III, article # 604640 Lot R11482, was incorrect.

Status: Terminated

Product Quantity: 23 units

Code Information:

Catalog # 604640, Lot Code R11428 21 units Catalog # 604642S, Lot Code R09071 1 unit

Distribution Pattern:

USA Nationwide Distribution in the states of: FL. OH, TX, & VA

Voluntary or Mandated:

Voluntary: Firm initiated