Iantrek Recalls

2 recalls found for Iantrek. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DEVICE

Iantrek Recalls C-Rex UNO Goniotomy Instrument Over Sterility Risk

Iantrek recalled 198 C-Rex UNO Microinterventional Goniotomy Instruments on September 6, 2025, due to compromised sterile packaging. The recall affects the model CRX-120 distributed in multiple U.S. states. Healthcare providers and patients must stop using these instruments immediately.

Iantrek
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Iantrek Recalls Cyclopen Microinterventional System Over Sterility Risk

Iantrek recalled 1,262 units of the Cyclopen Microinterventional Cyclodialysis System on September 6, 2025. The recall stems from a risk of compromised sterile packaging that could affect patient safety. Health care providers and patients must stop using the device immediately and follow manufacturer instructions.

Iantrek
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Brand Statistics

Total Recalls
2
Pages
1