International Life Sciences recalls Artelon FlexBand Plus models 41054 and 41057 due to failed bacterial endotoxin testing. Consumers should check product details and contact the company for remedies.
Augmentation devices failed bacterial endotoxin testing.
International Life Sciences is recalling Artelon FlexBand Plus devices with specific reference numbers because they failed bacterial endotoxin testing. This means the products could pose a health risk if used as intended.
The devices failed bacterial endotoxin testing, which means they may contain harmful bacteria. This could lead to infections or health issues if used without proper cleaning or sterilization.
Users of Artelon FlexBand Plus devices with reference numbers 41054 or 41057 are affected. Those with the specific lot numbers or GTINs listed are most at risk.
Check for reference numbers 41054 or 41057 on the product. Look for lot numbers A10010201 or A10010101 and GTINs 00850003396064 or 00850003396033.
Identify the reference number and lot information on your Artelon FlexBand Plus device.
The Artelon FlexBand Plus devices failed bacterial endotoxin testing, which means they may contain harmful bacteria.
The recall record does not specify a remedy, so contact International Life Sciences directly for instructions.
Check for reference numbers 41054 or 41057, lot numbers A10010201 or A10010101, and GTINs 00850003396064 or 00850003396033.
We’ve drafted a message you can send International Life Sciences to request your refund or repair — edit it as you like.
Subject: Recall Z-1555-2026 — International Life Sciences International Life Sciences Hello, I own a International Life Sciences that is covered by recall Z-1555-2026 from International Life Sciences. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
