Iantrek recalls C-Rex UNO Microinterventional Goniotomy Instrument (model CRX-120) due to potential compromised sterile packaging. This could affect surgical safety during ophthalmic procedures.
Potential for compromised integrity of the sterile packaging.
Iantrek is recalling its C-Rex UNO Microinterventional Goniotomy Instrument (model CRX-120) because the sterile packaging might be damaged, risking infection during eye surgery. This is a serious hazard for medical professionals using the instrument.
The sterile packaging may become compromised, leading to contamination of the surgical instrument. This could cause infections or other complications during eye surgery procedures.
Medical professionals who use the C-Rex UNO instrument for eye surgery are most at risk. Patients undergoing ophthalmic procedures with this instrument could be affected.
Check for model number CRX-120 on the instrument. The lot numbers are 351729 or 351759 with expiration dates of May 2026.
Immediately stop using the C-Rex UNO Microinterventional Goniotomy Instrument if it has model number CRX-120.
The model number is CRX-120.
Compromised sterile packaging could lead to contamination of the surgical instrument, risking infection during eye surgery.
Check for model number CRX-120 and lot numbers 351729 or 351759 with expiration dates of May 2026.
We’ve drafted a message you can send Iantrek to request your refund or repair — edit it as you like.
Subject: Recall Z-0135-2026 — Iantrek Iantrek Hello, I own a Iantrek that is covered by recall Z-0135-2026 from Iantrek. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
