Recall Ledger

Artelon FlexBand Plus Ref: 41054 & 41057 recall (International Life Sciences)

Medical deviceClass IIOngoing

Summary: International Life Sciences is recalling Artelon FlexBand Plus Ref: 41054 & 41057. Reason: Augmentation devices failed bacterial endotoxin testing.

What is being recalled

Artelon FlexBand Plus Ref: 41054 & 41057

Why

Augmentation devices failed bacterial endotoxin testing.

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

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. (states named: Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, Nebraska, New Jersey, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, Wyoming)

How to tell if yours is affected

REF: 41054 -Lot: A10010201/GTIN: 00850003396064 REF: 41057 - Lot: A10010101/GTIN: 00850003396033

What to do

Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.

Recall facts

Recall numberZ-1555-2026
CategoryMedical device
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedFebruary 6, 2026
ReportedMarch 18, 2026
CompanyInternational Life Sciences
Company locationAtlanta, GA, United States
Initiated byVoluntary: Firm initiated
QuantityN/A

More recalls from International Life Sciences · all medical device recalls · recalls from February 2026

Official FDA record