DePuy Mitek, Inc., a Johnson & Johnson Co.: Medical Device Recall in 2025 - (Recall #: Z-1314-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

COR Disposable Kit, 8 mm. Cartilage Transplant System.

Product Classification:

Class II

Date Initiated: February 24, 2025

Date Posted: March 19, 2025

Recall Number: Z-1314-2025

Event ID: 96347

Reason for Recall:

Device is missing the pin in the graft loader component.

Status: Ongoing

Product Quantity: US: 131 units; OUS: 312 units

Code Information:

Model No. 252109 & 252112; GTIN: 10886705012374 & 10886705012404; Lot No. 23C11, 23C12, 23E04, 23F02, 23R03, 24A02, 24B01, 24C17, 24P07, 23C13, 23D03, 23D14, 23F01, 24C15, 24K07 & 24N10.

Distribution Pattern:

Domestic: Nationwide Distribution; Foreign: Austria, Belgium, Brazil, Switzerland, Chile, China, Colombia, Czech Republic, Germany, Spain, Finland, France, French Guyana, Greece, Israel, India, Italy, Japan, South Korea, Luxemburg, Mexico, Netherlands, Poland, Portugal & Singapore.

Voluntary or Mandated:

Voluntary: Firm initiated