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International Life Sciences recalls Artelon FlexBand Plus Ref: 41054 & 41057
Recalled March 18, 2026 · FDA recall Z-1555-2026 · International Life Sciences
Hazard
Augmentation devices failed bacterial endotoxin testing. · FDA Class II
Units
N/A
Sold at
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, MI, MN, MO, MS, MT, NC, NE, NJ, NY, OH, OK, OR, PA, SD, TN, TX, UT, VA, WA, WI, WY and the countries of Australia, France, Germany, Italy, Japan, Korea, Spain, Switzerland, United Kingdom, United Arab Emirates, Slovenia.
Description
Augmentation devices failed bacterial endotoxin testing.
Product
Artelon FlexBand Plus Ref: 41054 & 41057
Manufacturer(s)
International Life Sciences
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →