PlainRecalls
FDA Devices Moderate Class II Terminated

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

Reported: July 5, 2017 Initiated: May 30, 2017 #Z-2624-2017

Product Description

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

Reason for Recall

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

Details

Recalling Firm
Smith & Nephew, Inc.
Units Affected
36 units
Distribution
US distribution to TN
Location
Memphis, TN

Frequently Asked Questions

What product was recalled?
LEGION(R) FEM CONE IMPACTOR HEADS: a) REF 71441976, ID 18MM b) REF 71441977, ID 20MM c) REF 71441978, ID 22MM. Recalled by Smith & Nephew, Inc.. Units affected: 36 units.
Why was this product recalled?
The incorrect Loctite adhesive was used to assemble the impactor heads.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 5, 2017. Severity: Moderate. Recall number: Z-2624-2017.