Corin Ltd: Medical Device Recall in 2022 - (Recall #: Z-1509-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Corin METAFIX HIP STEM, SIZE 3, STANDARD, 135 degrees, COLLARED HIP STEM, CEMENTLESS, Part Number 579.0103

Product Classification:

Class II

Date Initiated: July 22, 2022

Date Posted: August 17, 2022

Recall Number: Z-1509-2022

Event ID: 90573

Reason for Recall:

One MetaFix size 7 collarless stem from batch 478179 which was incorrectly labelled as a MetaFix size 3 collared stem from batch 485630.

Status: Ongoing

Product Quantity: 5 devices

Code Information:

UDI (01) 0 505563 89123 0 (10) 485630 (17) 261114, Lot Number 485630

Distribution Pattern:

US Nationwide distribution in the states of OK, TX, FL.

Voluntary or Mandated:

Voluntary: Firm initiated