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FDA DeviceClass IINotable

FDA Recall: Artelon FlexBand Dynamic Matrix Ref: 31057

Date: 2026-03-18
Brand: International Life Sciences
Category: Medical Device
FDA Class: Class II

Description

Augmentation devices failed bacterial endotoxin testing.

Hazard

Augmentation devices failed bacterial endotoxin testing.

Remedy

N/A

View original recall →
FDA Recall: Artelon FlexBand Dynamic Matrix Ref: 31057 | RecallWatch