Smith & Nephew, Inc.: Medical Device Recall in 2017 - (Recall #: Z-2625-2017)

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) TIB CONE IMPACTOR HEADS: a) REF 71441972, ID 24MM b) REF 71441971, ID 22MM c) REF 71441973, ID 26MM d) REF 71441974, ID 28MM e) REF 71441975, ID 30MM

Product Classification:

Class II

Date Initiated: May 30, 2017

Date Posted: July 5, 2017

Recall Number: Z-2625-2017

Event ID: 77413

Reason for Recall:

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

Status: Terminated

Product Quantity: 46 units

Code Information:

Lot numbers: a) 16HGA0040 b) 16JGA0003 c) 16JGA0005 d) 16JGA0006 e) 16JGA0007

Distribution Pattern:

US distribution to TN

Voluntary or Mandated:

Voluntary: Firm initiated