Biomet Spine, LLC: Medical Device Recall in 2015 - (Recall #: Z-2744-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Biomet Parsippany, NJ. 4 0 MM X 14 MM Variable Screw C-Tek Maxan Anterior Cervical Plate System. Lot 375440.

Product Classification:

Class II

Date Initiated: August 5, 2015

Date Posted: September 16, 2015

Recall Number: Z-2744-2015

Event ID: 71940

Reason for Recall:

Some of P/N 14-521614B Lot 375440 was mislabeled as P/N 14-521614 Lot 375440.

Status: Terminated

Product Quantity: 7 parts

Code Information:

Model Number 14-521614B, lot number 375440.

Distribution Pattern:

Nationwide Distribution including Distributed nationwide to OH, LA, TX, and GA.

Voluntary or Mandated:

Voluntary: Firm initiated