International Life Sciences
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...
Source: openFDA Enforcement API