Cardinal Health recalls Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter 16 Fr/Ch (5.3 mm) Product Code 3408 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 Hydrogel Coated Catheters because a blockage in the bubble inlet port may prevent proper urine drainage, increasing the risk of urinary retention. Patients using this product should stop using it immediately to avoid potential complications.
The bubble inlet port can become blocked, preventing urine from draining into the collection bag. If urine isn't drained properly, it can lead to urinary retention, which may require medical intervention.
Patients using the Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter 16 Fr/Ch (5.3 mm) Product Code 3408 are affected. Those with urinary drainage systems using this specific product are most at risk.
Check for the product code 3408 on the packaging. The item was sold with lot numbers 2215825664 and case numbers 10884521009431 and 20884521009438.
Immediately stop using the Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter 16 Fr/Ch (5.3 mm) Product Code 3408 if you have it.
The product code is 3408.
Lot number 2215825664 is affected.
If you have the Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter 16 Fr/Ch (5.3 mm) Product Code 3408, you should stop using it immediately to prevent urinary retention risk.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-0357-2023 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-0357-2023 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.
