Encore Medical, Lp: Medical Device Recall in 2015 - (Recall #: Z-0131-2016)

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:

AltiVate Humeral Socket Shell Trial, Part Number 804-06-052 The glenoid baseplate is intended for cementless application with addition of screws for fixation. The humeral stem is intended for cemented or cementless use. This device may also be indicated in the salvage of previously failed surgical attempts. Shoulder reconstructive surgery should be reserved for patients who have failed non-operative treatments.

Product Classification:

Class II

Date Initiated: September 15, 2015

Date Posted: October 28, 2015

Recall Number: Z-0131-2016

Event ID: 72208

Reason for Recall:

Difficulty assembling the shell trial to the broach and the retaining ring disassembled from the screw.

Status: Terminated

Product Quantity: 20 units

Code Information:

Lot: 180052L01

Distribution Pattern:

US Distribution to states of: PA, FL, ID, and CA.

Voluntary or Mandated:

Voluntary: Firm initiated