International Life Sciences 2026-03-18 Health serious FDA
Health · FDA · Recall #FDA-Z-1554-2026
Artelon FlexBand Dynamic Matrix Ref: 31057 Recall
Issued March 18, 2026 · International Life Sciences
In March 2026, International Life Sciences recalled the Artelon FlexBand Dynamic Matrix Ref: 31057, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Augmentation devices failed bacterial endotoxin testing.
What you should do
- 1 Stop using Artelon FlexBand Dynamic Matrix Ref: 31057 right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact International Life Sciences to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- International Life Sciences
- Category
- Health
- Recall date
- March 18, 2026
- Units affected
- Not reported
- 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
- Recall number
- FDA-Z-1554-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- International Life Sciences has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 356th Health recall we've logged in 2026.