Recall Z-2608-2021 · MEH Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
Corin Ltd
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.
| Date | Jul 28, 2021 |
| Status | Terminated |
| Reason | 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. |
| Root cause | Storage |
| Action | On 7/28&29/2021, the firm sent emails entitled "IMPORTANT-containment request FA COUK 2021 013" which notified the consignee they have been identified as receiving one or more of the medical devices listed in the attached Excel file due to them potentially having physical and/or water damage. They were to quarantine the parts until further instructions were issued. On 9/7/2021, Corin USA issued recall letters dated 9/3/2021 via email on 9/7/2021 requesting the devices be quarantined and returned. |
| Quantity | 2 |
| Distribution | US Nationwide distribution in the states of AZ, CA, FL, IL, OK, PA, TX, UT, and WI. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K170359 | Trinity Dual Mobility System Corin U.S.A. Limited, Oct 31, 2017 |