Carwild recalls Ivalon CELLULOSE SURGICAL SPEAR models Q604237 with LOT 24G1739 due to potential sterile barrier failure during ophthalmic surgery.
Potential for package seal to be out of specification and the sterile barrier cannot be guaranteed for the life of the product.
Carwild is recalling Ival:on surgical spears used in eye surgery because the packaging might not stay sterile. This could lead to infections if the product is used without proper sterility.
The sterile packaging might not stay sealed properly, which could allow contamination. This means the surgical spear might not be sterile when used, increasing infection risk during eye surgery.
Surgical teams using the Ivalon CELLULOSE SURGICAL SPEAR during eye procedures are affected. Patients and staff at hospitals using the recalled model are at risk of infection.
Check for model number Q604237 and lot number 24G1739 on the packaging. The product is intended for ophthalmic surgical procedures for fluid management.
Look for model number Q604237 and lot number 24G1739 on the packaging.
The recall states the sterile barrier might not be guaranteed, so it's not safe to use without checking the recall.
The recall does not specify a remedy, so check with Carwild for guidance.
Look for model number Q604237 and lot number 24G1739 on the packaging.
We’ve drafted a message you can send Carwild to request your refund or repair — edit it as you like.
Subject: Recall Z-0799-2025 — Carwild Carwild Hello, I own a Carwild that is covered by recall Z-0799-2025 from Carwild. 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.
