International Life Sciences Recalls

3 recalls found for International Life Sciences. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DEVICE

International Life Sciences Recalls Artelon FLEXBAND TWIST Augmentation Devices for Endotoxin Test F

International Life Sciences issued an active recall of Artelon FLEXBAND TWIST augmentation devices. The devices were distributed worldwide, including nationwide in the United States. The recall concerns failures in bacterial endotoxin testing that could pose a infection risk; users should stop using the device and follow recall instructions from the manufacturer.

International Life Sciences
Augmentation devices
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Health & Personal Care
HIGH
FDA DEVICE

International Life Sciences Recalls Artelon FlexBand Plus Augmentation Devices for Endotoxin Testing

International Life Sciences recalled Artelon FlexBand Plus augmentation devices after endotoxin testing failures. The recall affects devices with REF 41054 and REF 41057 distributed worldwide. Patients and healthcare providers must stop using the devices immediately and follow manufacturer instructions for recall return.

International Life Sciences
Augmentation devices
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Brand Statistics

Total Recalls
3
Pages
1

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