International Life Sciences
3 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for International Life Sciences and translate it into plain English — free weekly digest, optional same-day alerts.
- 2026-03-18FDA-DeviceClass IIStop using Artelon FLEXBAND TWIST devices
International Life Sciences is recalling Artelon FLEXBAND TWIST surgical augmentation devices (lot RK29976) because they failed bacterial endotoxin testing. Bacterial endotoxins are substances that can trigger harmful immune responses if present on medical devices used in surgery.
- 2026-03-18FDA-DeviceClass IIStop using Artelon FlexBand Plus devices
International Life Sciences is recalling Artelon FlexBand Plus augmentation devices (Ref: 41054 and 41057) because they failed bacterial endotoxin testing. These devices may contain harmful bacterial contamination that could cause infection or other complications if implanted.
- 2026-03-18FDA-DeviceClass IIStop using Artelon FlexBand Dynamic Matrix devices
International Life Sciences is recalling Artelon FlexBand Dynamic Matrix augmentation devices (Ref: 31057) because they failed bacterial endotoxin testing. Bacterial endotoxins are substances that can trigger harmful immune responses. The devices were distributed worldwide, including throughout the United States and multiple international markets.
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