Medline Aqua-Seal Chest Drainage Units for Adults Only: Updated Instructions
Medline recalls specific Aqua-Seal Chest Drainage Units (models DYNJ902487A, DYNJ908126, DYNJ910851) for adults 18+ due to updated instructions clarifying target patient age.
Lower-risk recall
The instructions for use (IFUs) on specified Cardinal Health Chest Drainage Units (CDUs) and accessories have been updated to clarify the intended target patient population as adults, 18 years and older.
Contact the company
What happened, in plain English
Medline is recalling certain Aqua-Seal Chest Drainage Units that were previously labeled for use on children. The recall updates instructions to specify these units are intended for adults 18 years and older only. This change ensures proper use for the intended patient group. Read more at govinfonow.com/recall/50063-medline-aqua-seal-chest-drainage-units-for-adults-only-updated.
Source Summary by GovInfoNow · govinfonow.com/recall/50063-medline-aqua-seal-chest-drainage-units-for-adults-only-updated · Updated August 10, 2026 · FDA enforcement record: FDA #Z-1562-2026
Cite this page
“Medline Aqua-Seal Chest Drainage Units for Adults Only: Updated Instructions.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/50063-medline-aqua-seal-chest-drainage-units-for-adults-only-updated. Based on FDA recall #Z-1562-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1562-2026%22&limit=1).
Why it’s dangerous
The units were previously sold without clear age restrictions, potentially leading to use on children. The recall updates instructions to specify they are intended for adults 18 years and older, reducing the risk of inappropriate use.
Who’s affected
Healthcare professionals using these specific Medline kits with Cardinal Health Aqua-Seal Chest Drainage Units. Children under 18 are not at risk as the units are now clearly labeled for adults only.
How to tell if you have this one
Check for model numbers DYNJ902487A (OPEN HEART), DYNJ908126 (CARDIAC PROCEDURE), or DYNJ910851 (CARDIO CONGENITO) with specific lot numbers listed in the recall notice.
- Brand
Medline- Category
Medical device
What to do — step by step
Check Product Model
Identify the model number (DYNJ902487A, DYNJ908126, or DYNJ910851) and lot number from the product label.
Verify Age Appropriateness
Ensure the unit is intended for adult patients (18 years and older) as per updated instructions.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Worldwide - US Nationwide distribution in the state of CA and the countries of Chile, Panama.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 47 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.
Questions people ask
What should I do if I have one of these units?
Check the model number and lot number against the list provided in the recall notice to confirm if it's affected.
Is there a risk of injury from using these units on children?
The recall addresses potential misuse on children by updating instructions to specify adult use only. No injury reports were mentioned in the recall.
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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-1562-2026 (January 30, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1562-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 10, 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.