medical MODERATE Updated 2026-03-18

International Life Sciences recalls Artelon FlexBand Dynamic Matrix Ref: 31057

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Recalled Product

Artelon FlexBand Dynamic Matrix Ref: 31057

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Hazard / Issue

Augmentation devices failed bacterial endotoxin testing.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: A10011001/GTIN: 00850003396019

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for Artelon FlexBand Dynamic →

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View official government recall

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