Smith & Nephew, Inc.: Medical Device Recall in 2021 - (Recall #: Z-0772-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Bone fixation nail. TRIGEN INTERTAN - Product Usage: indicated for fractures of the femur including simple shaft fractures, comminuted shaft fractures, spiral shaft fractures, long oblique shaft fractures and segmental shaft fracture;

Product Classification:

Class II

Date Initiated: November 2, 2020

Date Posted: January 13, 2021

Recall Number: Z-0772-2021

Event ID: 86927

Reason for Recall:

Manufacturing packaging error.

Status: Terminated

Product Quantity: 41 units

Code Information:

Model #: 71675535 & 71675532 Lot #: 20CM25278 & 20DM01466.

Distribution Pattern:

Worldwide distribution - US Nationwide distribution including in the states of AL, AZ, CA, FL, IA, KY, MI, NC, NJ, OH, PA, TN, TX, WA and the countries of AU, CA & GB.

Voluntary or Mandated:

Voluntary: Firm initiated