Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 20208 |
| Brand Name: | Ethicon Physiomesh Composite mesh |
| Model: | PHY0715R PHY1015V PHY1515Q PHY1520R PHY1520V PHY2025V PHY2030R PHY2535V PHY3035R and PHY3050R |
| Affected: | All lots |
| Software version: | |
| Recalling Organisation: | Johnson & Johnson (New Zealand) Limited 507 Mt Wellington Highway Mt Wellington AUCKLAND 1060 |
| Contact Information: | 0800 922 638 |
| Manufacturer: | Johnson & Johnson International |
| Issue: | Manufacturer has initiated worldwide medical device removal of product from the market. . Health Canada issued Medical Recall RECALL 25May2016 (RA-58846) . MHRA Recall 2016/005/025/701/005 -Health care practitioners that have treated patients using ETHICON PHYSIOMESH™ Composite Mesh should continue to follow those patients in the usual manner.This voluntary recall has been communicated to the U.S. ,Food and Drug Administration (FDA) and the European Competent Authorities |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 30/5/2016 |
