← FDA ENFORCEMENT
Z-2132-2026Class II

Orthorebirth Co Ltd

Recalling firm
Orthorebirth Co Ltd
Product type
Device
Status
Ongoing
Report date
2026-05-13
Distribution
US Nationwide distribution in the states of CA, FL.
Product quantity
20
Initiated by
Voluntary: Firm initiated
Reason for recall

Resorbable bone void filler falls outside standard specifications.

Product description

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

Code / lot info

UDI-DI: 04573190050637. Lots: 25F07104JF, 25F07105JF, 25F07106JF

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.