Smith & Nephew, Inc.: Medical Device Recall in 2017 - (Recall #: Z-2624-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

LEGION(R) FEM CONE IMPACTOR HEADS: a) REF 71441976, ID 18MM b) REF 71441977, ID 20MM c) REF 71441978, ID 22MM

Product Classification:

Class II

Date Initiated: May 30, 2017

Date Posted: July 5, 2017

Recall Number: Z-2624-2017

Event ID: 77413

Reason for Recall:

The incorrect Loctite adhesive was used to assemble the impactor heads.

Status: Terminated

Product Quantity: 36 units

Code Information:

Lot numbers: a) 16HGA0031 b) 16HGA0034 c) 16HGA0035

Distribution Pattern:

US distribution to TN

Voluntary or Mandated:

Voluntary: Firm initiated