Medline Central Line Dressing Tray Recall: Incomplete Seals Risk Sterility
Medline recalls Central Line Dressing Change Trays with potential incomplete seals that could compromise sterility. Affected units include Lot 2020021990 and Product Number DYNDC1928C.
Lower-risk recall
Potential of incomplete seals impacting the sterility of the kit.
Contact the company
What happened, in plain English
Medline is recalling Central Line Dressing Change Trays that may have incomplete seals, risking contamination of medical kits. This could lead to infections if used improperly. Read more at govinfonow.com/recall/64491-medline-central-line-dressing-tray-recall-incomplete-seals-risk-sterility.
Source Summary by GovInfoNow · govinfonow.com/recall/64491-medline-central-line-dressing-tray-recall-incomplete-seals-risk-sterility · Updated August 19, 2026 · FDA enforcement record: FDA #Z-3013-2020
Cite this page
“Medline Central Line Dressing Tray Recall: Incomplete Seals Risk Sterility.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/64491-medline-central-line-dressing-tray-recall-incomplete-seals-risk-sterility. Based on FDA recall #Z-3013-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3013-2020%22&limit=1).
Why it’s dangerous
Incomplete seals might allow contaminants to enter the sterile dressing kit during use. This could lead to infections if the kit is not properly sealed.
Who’s affected
Healthcare workers using central line dressing kits are most at risk. Patients receiving these treatments could face infection if the seals fail.
How to tell if you have this one
Check for Lot Number 2020021990 or Product Number DYNDC1928C on the tray. The recall applies to specific units sold by Medline.
- Brand
Medline- Category
Medical device
What to do — step by step
Check Product Details
Look for Lot Number 2020021990 or Product Number DYNDC1928C on the tray.
Where it went and when
Where it was distributed
Distributed in Minnesota and Texas.
FDA distribution: “Domestic Distribution: MN and TX.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Minnesota, Texas.
Recall timeline
FDA terminated this recall 9 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
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-3013-2020 (August 12, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3013-2020 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.