FDA Recall Open, Classified

ZENBONE, REF: ORB-0320C-Z, ORB-0310C-Z, ORB-0304C-Z

Recall: Z-2132-2026 · Initiated March 25, 2026

Recall

Recall Number
Z-2132-2026
Event Number
98733
Firm
Orthorebirth Co Ltd 3 Chome 17-43 Chigasakihigashi; Tsuzuki Yokohama Japan
FEI Number
3011415547
Product Code
MQV
Status
Open, Classified
Root Cause
Device Design
Initiated
March 25, 2026
Posted
May 7, 2026

Description

ZENBONE, REF: ORB-0320C-Z, ORB-0310C-Z, ORB-0304C-Z

Reason

Resorbable bone void filler falls outside standard specifications.

Action

On 3/25/2026, product withdrawal emails were sent to customers informing them to stop distribution and that additional information on device return would be provided. If products were distributed to distributors or hospitals, the firm requests the customer inform to stop distribution and ensure affected devices are not used. In addition, notify the firm if affected devices were used in surgery. On 4/21/2026, recall notices were emailed to customers who were asked to do the following: 1) Return affected devices to firm. 2) If devices were distributed elsewhere, recover all affected product that is in the hands of sub-distributors or end-users, and that you return all affected product to firm. 3) Complete and return the customer reply form via email to [email protected] If you have recall questions, an alternative firm contact for the recall can be found at 1-858-792-1235

Distribution

US Nationwide distribution in the states of CA, FL.

Quantity

20