Synthes (USA) Products LLC: Medical Device Recall in 2015 - (Recall #: Z-2086-2015)

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:

16mm Chisel Blade; used in the LCP Anterior Ankle Arthodesis Plate System and the Hip Preservation Surgery Set. Orthopedic manual surgical instrument.

Product Classification:

Class II

Date Initiated: June 24, 2015

Date Posted: July 22, 2015

Recall Number: Z-2086-2015

Event ID: 71599

Reason for Recall:

It was discovered that a 10mm Chisel Blade was etched as a 16mm Chisel Blade.

Status: Terminated

Product Quantity: 100

Code Information:

Part Number 399.56 Lot Numbers T106341

Distribution Pattern:

US Distribution to the states of : NJ, VA, OH, IN, MI, FL, WI, CA, TN, MD, NC, WA, UT, ID, MO, NV and KS.

Voluntary or Mandated:

Voluntary: Firm initiated