Carwild recalls Ival: 20cm eye wicks due to potential sterile barrier failure. This could compromise surgical site safety. Affected units have model Q604206 and lot 24G1880.
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 Ivalon Eye Wicks 20cm because the sterile packaging might not stay sealed properly. This could let contaminants reach the surgical site during use, risking infection.
The packaging seal might not stay intact, which could let unsterile materials contact the surgical site. This might increase infection risk during procedures.
Surgical staff and patients using these eye wicks during eye surgery. Those with model Q604206 and lot 24G1880 are most at risk.
Check for model number Q604206 and lot number 24G1880 on the packaging. These eye wicks are intended for ophthalmic surgical use.
Look for model Q604206 and lot 24G1880 on the packaging.
The sterile barrier might not stay sealed properly, increasing infection risk during eye surgery.
Model Q604206 with lot number 24G1880.
No specific stop-use instruction is given; check packaging for model and lot numbers.
We’ve drafted a message you can send Carwild to request your refund or repair — edit it as you like.
Subject: Recall Z-0798-2025 — Carwild Carwild Hello, I own a Carwild that is covered by recall Z-0798-2025 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.
