Avanos Medical recalls ambIT Reusable Program Luer Cass kits (Product Code 220568) due to potential distribution without an air in-line filter. Affected units have Lot Number 30191805 (expiring 17 Jan 2025).
Some of the ambIT kits were potentially distributed without an air in-line filter.
Avanos Medical is recalling some ambIT Reusable Program Luer Cass kits because they may have been distributed without an air in-line filter. This could pose a risk if the kit is used without the filter, though the specific danger isn't detailed in the recall.
The recall states that some kits were potentially distributed without an air in-line filter. This could mean that during use, the kit might not filter air properly, potentially introducing contaminants into the system. However, the recall does not specify the exact risk or how serious it is.
Users of the ambIT Reusable Program Luer Cass kits with Product Code 220568 and Lot Number 30191805 (expiring 17 January 2025) are affected. Medical professionals using these kits for procedures are most at risk.
Check for Product Code 220568 and Lot Number 30191805 (expiring 17 January 2025) on the ambIT Reusable Program Luer Cass kits. The product is manufactured by Avanos Medical, Inc.
Verify the Product Code (220568) and Lot Number (30191805) on the ambIT Reusable Program Luer Cass kit.
The recall states that some ambIT kits were potentially distributed without an air in-line filter, but the specific risk is not detailed in the notice.
The recall does not specify a remedy, so no action is required beyond checking the product details.
The recall does not describe a specific hazard mechanism or risk of serious injury.
We’ve drafted a message you can send Avanos Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1687-2023 — Avanos Medical Avanos Medical Hello, I own a Avanos Medical that is covered by recall Z-1687-2023 from Avanos Medical. 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.
