Corin Ltd: Medical Device Recall in 2021 - (Recall #: Z-2608-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Corin Trinity Dual Mobility, Size 4, Dual Mobility CoCr Liner, REF 321.04.540, Sterile, and Corin Dual Mobility, Size 4 42 insert/28 head, REF 325.04.042, Sterile; both are components of the Trinity Dual Mobility System.

Product Classification:

Class II

Date Initiated: July 28, 2021

Date Posted: October 6, 2021

Recall Number: Z-2608-2021

Event ID: 88589

Reason for Recall:

The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices.

Status: Terminated

Product Quantity: 2

Code Information:

The affected products are shipment specific and were delivered to the consignee between 7/22-26/2021. Model 321.04.540 - Lot number 478880 delivered 7/26/2021; Model 325.04.042- Lot number 480567 delivered 7/26/2021.

Distribution Pattern:

US Nationwide distribution in the states of AZ, CA, FL, IL, OK, PA, TX, UT, and WI.

Voluntary or Mandated:

Voluntary: Firm initiated