Medical DeviceOct 22, 2025
Iantrek C-Rex UNO Microinterventional Goniotomy Instrument recall — FDA Z-0135-2026
Potential for compromised integrity of the sterile packaging.
Class IIFDA: OngoingIantrek Inc.
Recall history in this database
Classification mix: Class II: 2.
Medical DeviceOct 22, 2025
Iantrek Cyclopen Microinterventional Cyclodialysis System recall — FDA Z-0134-2026
Potential for compromised integrity of the sterile packaging.
Class IIFDA: OngoingIantrek Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Iantrek Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.