Stryker Corporation: Medical Device Recall in 2018 - (Recall #: Z-0837-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

STRYKER WEDGE INTERFERENCE SCREW SYSTEM, ACL Interface Screw, 9MM X 25MM, Model 0234010056, labeled sterile.

Product Classification:

Class II

Date Initiated: November 17, 2017

Date Posted: March 14, 2018

Recall Number: Z-0837-2018

Event ID: 78668

Reason for Recall:

Routine bioburden testing of certain lots were found to have levels higher than internal acceptable rates.

Status: Terminated

Product Quantity: 60,753 units total

Code Information:

Model 0234010056, UDI 04546540754561, Lot No. 17278AG2

Distribution Pattern:

Distributed domestically to . Distributed internationally to Australia and Mexico.

Voluntary or Mandated:

Voluntary: Firm initiated