International Life Sciences

Device Recalls (Class II)

← All Device Recalls (Class II)
Class II Z-1554-2026 · 20260318 · Ongoing

Product

Artelon FlexBand Dynamic Matrix Ref: 31057

Reason for Recall

Augmentation devices failed bacterial endotoxin testing.

Distribution

Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, M...