DePuy Orthopaedics, Inc.: Medical Device Recall in 2018 - (Recall #: Z-0848-2018)

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:

Concorde Lift Driver Shaft AO. Used with supplemental internal spinal fixation systems that have been cleared for use in the lumbar spine.

Product Classification:

Class II

Date Initiated: July 26, 2017

Date Posted: March 14, 2018

Recall Number: Z-0848-2018

Event ID: 79072

Reason for Recall:

Potential for Intra-operative breakage of driver tips

Status: Terminated

Product Quantity: 130 units total

Code Information:

Product code: 287804101G Lot number: 052316-A R, 121416-A R

Distribution Pattern:

Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated