Medline Umbilical Tray Recall: Packaging Defect Risk
Medline recalls umbilical trays with possible packaging defects that could compromise sterile product protection. Affected units include specific lot numbers and model UVT1250.
Lower-risk recall
There is a possible packaging defect impacting the outer Tyvec pouch that protects the sterile product.
Contact the company
What happened, in plain English
Medline is recalling umbilical trays with specific model and lot numbers due to a possible packaging defect that might compromise sterile product protection. This could lead to contamination risks during medical procedures. Read more at govinfonow.com/recall/52263-medline-umbilical-tray-recall-packaging-defect-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/52263-medline-umbilical-tray-recall-packaging-defect-risk · Updated August 18, 2026 · FDA enforcement record: FDA #Z-1995-2025
Cite this page
“Medline Umbilical Tray Recall: Packaging Defect Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/52263-medline-umbilical-tray-recall-packaging-defect-risk. Based on FDA recall #Z-1995-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1995-2025%22&limit=1).
Why it’s dangerous
The outer Tyvec pouch that protects the sterile product may have a packaging defect. This could allow contamination of the sterile product during medical procedures if the pouch fails.
Who’s affected
Healthcare professionals using Medline umbilical trays with model UVT125:3.5&5FR Catheter. Those most at risk are medical staff handling the trays during procedures.
How to tell if you have this one
Check for model UVT1250 with lot numbers 25BBG881, 24KBU973, 24IBK851, or 24HBQ012. The product is sold under the brand Medline.
- Brand
Medline- Category
Medical device
What to do — step by step
Check Product Details
Identify the model number (UVT1250) and lot numbers (25BBG881, 24KBU973, 24IBK851, 24HBQ012) to confirm if your item is affected.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide distribution in the state of VA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 48 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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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-1995-2025 (May 15, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1995-2025 to see it in context.
- Plain-language summary written by qwen3:4b on August 18, 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.