International Life Sciences recalls Artelon FlexBand Plus Ref: 41054 & 41057
- Recalling company
- International Life Sciences
- Product
- Artelon FlexBand Plus Ref: 41054 & 41057
- Reason
- Augmentation devices failed bacterial endotoxin testing.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Feb 6, 2026
- Reported
- Mar 18, 2026
- 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, 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.
- Status
- Ongoing
- Quantity
- N/A
- Lot / codes
- REF: 41054 -Lot: A10010201/GTIN: 00850003396064 REF: 41057 - Lot: A10010101/GTIN: 00850003396033
- Company location
- Atlanta, GA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1555-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1555-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.