DePuy Orthopaedics, Inc.: Medical Device Recall in 2017 - (Recall #: Z-2317-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

DePuy Synthes various orthopedic instruments modified by U.S. Distributors These instruments are used in various orthopedic procedures

Product Classification:

Class II

Date Initiated: January 6, 2017

Date Posted: June 14, 2017

Recall Number: Z-2317-2017

Event ID: 76023

Reason for Recall:

Products were made outside of Quality System Regulation, and potentially outside of premarket submission (510k/PMA) for certain devices. The safety or effectiveness of these devices cannot be assured.

Status: Terminated

Product Quantity: 345

Code Information:

Unknown

Distribution Pattern:

Nationwide Distribution to: AZ CA IA IL IN LA MA MD ME MI MN PA VA

Voluntary or Mandated:

Voluntary: Firm initiated