Avanos Medical recalls specific models of BALLAD Multi-Access Port Catheters due to incorrect expiration dates on some units. Affected products may have expired dates that could lead to improper use.
Product was distributed with incorrect expiration date.
Avanos Medical is recalling certain BALLAD Multi-Access Port Catheters because they were distributed with incorrect expiration dates. This could lead to improper use if the product is used after its expiration date.
The product was distributed with incorrect expiration dates. If used after the expiration date, it could lead to improper use or potential complications in medical procedures.
Patients using the recalled catheters for medical treatments. Healthcare providers who administer these catheters are most at risk of using expired products.
Check for the product name 'BALLAD Multi-Access Port Catheter, Double Swivel Y Elbow, Adult, 14 French; Sterile; Single Use'. Look for lot numbers: 20065842, 30135996, 30135999, 30137463, 30140309, 30138711, or 30141360.
Verify the expiration date on the product label to ensure it is valid.
The recall record does not specify the correct expiration date.
Check for the lot numbers listed: 20065842, 30135996, 30135999, 30137463, 30140309, 30138711, or 30141360.
The recall does not require immediate stop use; check the expiration date to ensure it is valid.
We’ve drafted a message you can send Avanos to request your refund or repair — edit it as you like.
Subject: Recall Z-0846-2022 — Avanos Avanos Hello, I own a Avanos that is covered by recall Z-0846-2022 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.
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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.
