Cardinal Health recalls Dover Closed Urethral Tray with Vinyl Catheter (Product Code 3420) due to potential blockage in the drainage bag 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 Vinyl Catheter (Product Code 3420) because blockage in the drainage bag may prevent urine from draining, increasing the risk of urinary retention. This is a serious medical risk for patients using catheters.
The drainage bag's bubble inlet port can become blocked, preventing urine from flowing into the bag. If urine isn't drained properly, it can lead to urinary retention, which may cause discomfort, infection, or other complications.
Patients using catheters for urinary drainage are affected. Those with urinary retention risks or who use the product for extended periods are most at risk.
Check for Product Code 3420 on the tray. The lot numbers are 2215000364 and the case number is 20884521009452. This product was sold with UDI-DI: 10884521009455.
Inspect the bubble inlet port for blockage; if blocked, contact your healthcare provider immediately.
The product may have a blockage risk that could lead to urinary retention, so it's not safe to use without checking for blockage.
Check the bubble inlet port for blockage; if blocked, contact your healthcare provider immediately.
Look for Product Code 3420, lot number 2215000364, or case number 20884521009452 on the tray.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-0359-2023 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-0359-2023 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.
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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.
