DePuy Mitek, Inc., a Johnson & Johnson Co.: Medical Device Recall in 2019 - (Recall #: Z-0665-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Healix Knotless ADV BR 4.75 Suture Anchor

Product Classification:

Class II

Date Initiated: November 4, 2019

Date Posted: December 18, 2019

Recall Number: Z-0665-2020

Event ID: 84237

Reason for Recall:

Specific product codes and lots of the Mitek HEALIX ADVANCE" Knotless Anchors were manufactured with BIOCRYL" Biocomposite Material instead of BIOCRYL RAPIDE¿ Biocomposite Material. BIOCRYL and BIOCRYL RAPIDE are biocompatible and effective material choices for absorbable, injection-molded sports medicine implant fixation.

Status: Terminated

Product Quantity: 299

Code Information:

Part Number: 222330 Batch/Lot: 5L45257 GTIN: 10886705023462

Distribution Pattern:

US: AL AZ CA CT FL IA IL IN LA MA MD ME MI MN MT NC NE NH NJ NM OH OK OR PA TN TX VA WA WI International: Belgium, Chile, China, Czech Republic, France, India, Japan, Korea, Latvia, New Zealand, Slovakia Sweden

Voluntary or Mandated:

Voluntary: Firm initiated