Cardinal Health recalls Dover Closed Urethral Tray with Hydrogel Coated Catheter due to risk of urinary drainage blockage, potentially causing urinary retention. Affected units have specific product codes and lot numbers.
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 hydrogel-coated catheters because a blockage in the drainage port could prevent urine from draining properly. This might lead to urinary retention if the bladder isn't emptied in time.
The device's bubble inlet port can become blocked, preventing urine from flowing into the drainage bag. If urine isn't drained regularly, it may cause urinary retention, which can lead to complications if not addressed.
Patients using this urinary drainage device for bladder emptying. Those with medical conditions requiring frequent catheter use are most at risk.
Check for product code 3410 and lot numbers: 2216502164, 2215825764, 2215122964, 2213740864, 2209525264, 2210223764. The device is intended for urinary drainage from the bladder.
Look for product code 3410 and the listed lot numbers on the device packaging.
The device is safe for use unless it has a blocked bubble inlet port, which could prevent proper urine drainage.
Check the product code and lot numbers to see if it's affected. If it is, contact Cardinal Health for instructions.
Yes, but monitor for blockage in the bubble inlet port. If urine isn't draining properly, stop use and contact a healthcare provider.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-0358-2023 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-0358-2023 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.
