Avanos recalls ambIT System PIB/PCA W 5in Cath (Product Code 220507) due to potential missing air in-line filter. Affected units sold with specific lot numbers through December 2023.
Some of the ambIT kits were potentially distributed without an air in-line filter.
Avanos is recalling some ambIT System PIB/PCA W 5in Cath kits because they might have been distributed without an air in-line filter. This could pose a risk if the filter is missing during medical use.
The ambIT kits may have been distributed without an air in-line filter. This filter is critical for preventing air embolisms during medical procedures. Without it, air could enter the bloodstream, potentially causing serious complications.
Patients using the ambIT System PIB/PCA W 5in Cath kits with Product Code 220507 are likely affected. Healthcare providers administering these kits are at higher risk due to the medical context.
Check for Product Code 220507 on the ambIT System PIB/PCA W 5in Cath kits. Affected units were sold with Lot Numbers 30177647 (expiring December 17, 2023) or 30174128 (expiring October 14, 2023).
Verify the Product Code on the ambIT System PIB/PCA W 5in Cath kit is 220507.
The recall is because some ambIT kits were potentially distributed without an air in-line filter, which is critical for preventing air embolisms during medical procedures.
Check the Product Code on the kit; if it's 220507, it may be affected. However, the recall record does not specify a remedy or action to take.
Yes, affected units have Lot Numbers 30177647 (expiring December 17, 2023) or 30174128 (expiring October 14, 2023).
We’ve drafted a message you can send Avanos to request your refund or repair — edit it as you like.
Subject: Recall Z-1685-2023 — Avanos Avanos Hello, I own a Avanos that is covered by recall Z-1685-2023 from Avanos. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
