Cardinal Health recalls Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 ml) 5ml Catheter Product Code: 2480 due to potential blockage of the bubble inlet port causing urinary retention risk.
Occlusion (blockage) of the bubble inlet port of the urinary drainage bag which may prevent urine draining into the bag. If the bladder is not emptied within a clinically appropriate time, this may increase the risk of urinary retention
Cardinal Health is recalling Dover Closed Urethral Trays with specific catheter sizes because a blockage in the bubble inlet port may prevent proper urine drainage, increasing the risk of urinary retention. This is a serious medical issue that requires immediate attention to avoid complications.
The bubble inlet port can become blocked, preventing urine from draining into the drainage bag. If urine isn't emptied regularly, it can lead to urinary retention, which may cause discomfort, infection, or other complications.
Patients using this catheter for urinary drainage are affected. Those with medical conditions requiring frequent catheter use are at higher risk.
Check for the product code 2480 on the catheter packaging. The lot numbers 2216501464, 2213046064, and 2206726764 are associated with this recall. This product was sold with specific UDI-DI numbers.
Look for product code 2480 on the catheter packaging to confirm if it's recalled.
Talk to your doctor or healthcare provider about the risk of urinary retention and possible alternatives.
The product may cause blockage of the bubble inlet port, which can lead to urinary retention. It is not safe to use without checking the recall status.
Contact your healthcare provider for guidance on managing the risk of urinary retention.
Check for product code 2480 and lot numbers 2216501464, 2213046064, or 2206726764 on the packaging.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-0356-2023 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-0356-2023 from Cardinal Health. 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.
