Cardinal Health recalls Dover Closed Urethral Tray with Vinyl Catheter due to potential blockage in the bubble inlet port, which may cause urinary retention if urine isn't drained properly.
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 models because a blockage in the bubble inlet port could prevent urine from draining into the bag. This risk might lead to urinary retention if the bladder isn't emptied regularly.
The bubble inlet port can become blocked, preventing urine from flowing into the drainage bag. If urine isn't drained properly, it may cause urinary retention, which requires medical attention.
Patients using the Dover Closed Urethral Tray with the specified catheter models and drainage bags. Those with urinary catheters are most at risk if the blockage occurs.
Check for the product code 3450LF on the tray. The lot numbers include 2216806064, 2214452064, 2212401164, 2210219764, 2209525364, 2208816464, 2206737964, and 2206727564. The product was sold with specific case and lot numbers.
Verify the product code 3450LF and lot numbers listed in the recall notice.
The Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 mm), 5 mL Catheter Pre-connected to 1000 mL Drainage Bag.
Check for product code 3450LF and lot numbers: 2216806064, 2214452064, 2212401164, 2210219764, 2209525364, 2208816464, 2206737964, or 2206727564.
The recall record does not specify a remedy.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-0361-2023 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-0361-2023 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.
