Avanos Medical recalls ambIT Kit Basic Filter Luer Cass (Product Code 220537) due to potential distribution without an air in-line filter. Affected units have specific lot numbers and expiration dates.
Some of the ambIT kits were potentially distributed without an air in-line filter.
Avanos Medical is recalling some ambIT Kit Basic Filter Luer Cass products because they might have been distributed without an air in-line filter. This could pose a risk if the filter is missing during use.
The ambIT kit is designed for medical use and requires an air in-line filter to function properly. Without this filter, the product may not work as intended, potentially leading to improper medical outcomes.
Users of the ambIT Kit Basic Filter Luer Cass with Product Code 220537 and specific lot numbers are affected. Those using the product for medical purposes may be at higher risk if the filter is missing.
Check for Product Code 220537 on the ambIT Kit Basic Filter Luer Cass. Affected units have lot numbers 30195563 or 30190578 with an expiration date of January 17, 2025.
Verify the Product Code is 220537 and lot numbers are 30195563 or 30190578.
The ambIT Kit Basic Filter Luer Cass may have been distributed without an air in-line filter, which is necessary for proper medical function.
Check the Product Code and lot numbers to see if your unit is affected. If it is, you may need to contact Avanos Medical for further instructions.
The recall is due to potential distribution without an air in-line filter, but the record does not specify a 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-1686-2023 — Avanos Medical Avanos Medical Hello, I own a Avanos Medical that is covered by recall Z-1686-2023 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.
