Corin USA Limited: Medical Device Recall in 2016 - (Recall #: Z-1527-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Trinity Acetabular Shell Product Usage: Total Hip Replacement.

Product Classification:

Class II

Date Initiated: January 29, 2016

Date Posted: May 4, 2016

Recall Number: Z-1527-2016

Event ID: 73205

Reason for Recall:

Potential for abrasion of the sterile barrier pouches of the new packaging system.

Status: Terminated

Product Quantity: 629 devices in total

Code Information:

Cluster Shell 044mm Taper Size 1, Lot Code: 320023; Cluster Shell 046mm Pager Size 2, Lot Code: 320018; Cluster Shell 048mm Taper Size 2, Lot Codes: 321691, 322402, 322981, 322982, 323745, 323746, 324298; Cluster Shell 050mm Taper Size 2, Lot Codes: 321954, 322753, 322980; Cluster Shell 050mm Taper Size 3, Lot Codes:

Distribution Pattern:

Worldwide Distribution - US Nationwide in the states of CA, FL, ID, TX, OK, OH, MA, and NC and the countries of Australia Belgium, Egypt, Germany, Ghana, Italy, Japan, Poland, South Africa and UK.

Voluntary or Mandated:

Voluntary: Firm initiated