Carwild recalls nasal packing used in eye surgery due to potential sterile barrier failure. Affected units have model Q770410 and lot 24F1638. No remedy specified in recall notice.
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 nasal packing used during eye surgery because the sterile barrier might not stay sealed properly. This could lead to contamination or infection if the product isn't kept sterile.
The product's sterile barrier might not stay sealed correctly over time, which could allow contamination. This is a risk during eye surgery procedures where sterility is critical.
Surgical staff and patients who used the Ivalon nasal packing during eye procedures. Those with model Q770410 and lot 24F1638 are most at risk.
Check for model number Q770410 and lot number 24F1638 on the packaging. This nasal packing was intended for use during ophthalmic surgical procedures.
Look for model number Q770410 and lot number 24F1638 on the packaging.
The recall states the sterile barrier might not stay sealed properly, so it's not guaranteed to be sterile for the product's entire life.
The recall notice does not specify any remedy or action steps for affected products.
Check for model number Q770410 and lot number 24F1638 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-0800-2025 — Carwild Carwild Hello, I own a Carwild that is covered by recall Z-0800-2025 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.
