Spine Smith Partners LP: Medical Device Recall in 2013 - (Recall #: Z-0932-2013)

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:

Cynch Lordotic T-PLlF Implant. Intervertebral fusion device with bone graft, for use with supplemental fixation.

Product Classification:

Class II

Date Initiated: August 24, 2012

Date Posted: March 20, 2013

Recall Number: Z-0932-2013

Event ID: 62993

Reason for Recall:

Implants were incorrectly laser marked as 23mm instead of 28mm.

Status: Terminated

Product Quantity: 3 units

Code Information:

Part Number: 0609-2809-06, Lot: 39AQ

Distribution Pattern:

Distributed in Texas.

Voluntary or Mandated:

Voluntary: Firm initiated