Use caution Medical device recall · FDA · Published November 1, 2022

Cardinal Health Dover Closed Urethral Tray Recall: Blockage Risk

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.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-0356-2023Medical device Cardinal Health ›

Use caution until it’s fixed

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

Take action

Contact the company

Recalling firmCardinal Health777 West St · Mansfield, MA 02048-1122

✎ GovInfoNow plain-language explainer

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. Read more at govinfonow.com/recall/59784-cardinal-health-dover-closed-urethral-tray-recall-blockage-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/59784-cardinal-health-dover-closed-urethral-tray-recall-blockage-risk · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0356-2023

Cite this page

“Cardinal Health Dover Closed Urethral Tray Recall: Blockage Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/59784-cardinal-health-dover-closed-urethral-tray-recall-blockage-risk. Based on FDA recall #Z-0356-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0356-2023%22&limit=1).

Cardinal Health recalled Dover Closed Urethral Trays with Vinyl Catheters due to a blockage hazard that may prevent urine drainage, the FDA said on Nov. 1, 2022. The agency announced the Class II voluntary recall under number Z-0356-2023.

How to tell if you have it

Brand: Cardinal Health
Product: Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 ml) 5ml Catheter
Product Code: 2480
Lot Numbers: 2216501464, 2213046064, 2206726764

The hazard

The recall addresses occlusion 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.

Context

GovInfoNow's records show Cardinal Health has four other recalls on record since Oct. 2, 2013. Other recent recalls include a Nov. 2, 2021 surgical gown recall for sterility risk and an Aug. 4, 2021 syringe recall for air reintroduction risk. Similar product recalls include Medline urethral catheter tray recalls announced on May 4, 2026.

How to tell if you have this one

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.

Brand
Cardinal Health
Category
Medical device

FDA recall event · 6 products

All 6 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class II
Status
Ongoing
Distribution
Nationwide

Recall number	Product, codes & lots
Z-0356-2023	Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 ml) 5ml Catheter Product Code: 2480 Intended for urinary drainage from the bladder of a patient; UDI-DI: Each 10884521009370 Case 20884521009377 Lot Numbers: 2216501464, 2213046064, 2206726764
Z-0357-2023	Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter 16 Fr/Ch (5.3 mm) Product Code: 3408 Intended for urinary drainage from the bladder of a patient; UDI-DI: Each 10884521009431 Case 20884521009438 Lot Numbers: 2215825664
Z-0358-2023	Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter 14 Fr/Ch (4.7 mm) Product Code: 3410 Intended for urinary drainage from the bladder of a patient; UDI-DI: Each 10884521009448 Case 20884521009445 Lot Numbers: 2216502164, 2215825764, 2215122964 2213740864, 2209525264, 2210223764
Z-0359-2023	Dover Closed Urethral Tray with Vinyl Catheter Product Code: 3420 Intended for urinary drainage from the bladder of a patient; UDI-DI: Each 10884521009455 Case 20884521009452 Lot Numbers: 2215000364
Z-0360-2023	Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 mm), 5 mL Catheter Pre-connected to 1000 mL Drainage Bag Product Code: 3450 Intended for urinary drainage from the bladder of a patient; UDI-DI: Each 10884521009479 Case 20884521009476 Lot Numbers: 2216502264, 2216507864, 2215825864 2215119164, 2214451964, 2213740964 2213046464, 2212401364, 2212401264 2211101164, 2211101264, 2209515164 2210219664, 2209515264, 2209501064 2207800564, 2208816364, 2207401264 2207401164
Z-0361-2023	Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 mm), 5 mL Catheter Pre-connected to 1000 mL Drainage Bag Product Code: 3450LF Intended for urinary drainage from the bladder of a patient.; UDI-DI: Each 10884521009585 Case 20884521009582 Lot Numbers: 2216806064, 2214452064, 2212401164 2210219764, 2209525364, 2208816464 2206737964, 2206727564

Based on the official FDA remedy

What to do — step by step

Check Product Code
Look for product code 2480 on the catheter packaging to confirm if it's recalled.
Contact Healthcare Provider
Talk to your doctor or healthcare provider about the risk of urinary retention and possible alternatives.

Where it went and when

Where it was distributed

Distributed nationwide.

FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 43 days after the firm started it.

Nov 1, 2022Firm started the recall
Dec 2, 2022FDA classified it Class II
Dec 14, 2022Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Keep exploring

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Link to this recall

<a href="https://govinfonow.com/recall/59784-cardinal-health-dover-closed-urethral-tray-recall-blockage-risk">Cardinal Health Dover Closed Urethral Tray Recall: Blockage Risk (GovInfoNow)</a>

Where this comes from

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.

Official source: FDA Recall #Z-0356-2023 (November 1, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0356-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.