Lower riskMedical device recall · FDA · Published January 9, 2025
Medline Convenience Kits Recall: Reduced Skin Barrier Wear Time Risk
Medline recalls two convenience kits for procedures due to reports of shorter skin barrier protection time. Affected kits may need replacement to prevent skin injury during use.
Kits contain recalled components due to reports of reduced skin barrier wear time. This refers to a shorter duration that a skin barrier can effectively adhere to and protect the skin before it needs to be replaced.
Take action
Contact the company
📍Recalling firmMEDLINE INDUSTRIES, LP - Northfield3 Lakes Dr · Northfield, IL 60093-2753
✎ GovInfoNow plain-language explainer
Medline is recalling adult intubation trays and main dispense kits for procedures because they contain components that can cause skin barriers to wear out faster than intended. This means the skin protection might not last as long, increasing the risk of skin injury during medical procedures. Read more at govinfonow.com/recall/53135-medline-convenience-kits-recall-reduced-skin-barrier-wear-time-risk.
“Medline Convenience Kits Recall: Reduced Skin Barrier Wear Time Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/53135-medline-convenience-kits-recall-reduced-skin-barrier-wear-time-risk. Based on FDA recall #Z-1182-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1182-2025%22&limit=1).
The FDA announced on Jan. 9, 2025, that Medline Industries LP is recalling 70 Medline Convenience Kits due to recalled components with reduced skin barrier wear time. Owners should contact the company for a remedy.
How to tell if you have it
Brand: Medline
Product: ADULT INTUBATION TRAY, Model Number DYNJAA254A, Lot Numbers 24KBR956, 24LBA655
Product: ADULT MAIN DISP. INTUB PART A, Model Number DYNJAA262A, Lot Number 24LBD397
Distribution: CA, NY
The hazard
The kits contain recalled components due to reports of reduced skin barrier wear time. This refers to a shorter duration that a skin barrier can effectively adhere to and protect the skin before it needs to be replaced.
Context
GovInfoNow's records show MEDLINE INDUSTRIES, LP - Northfield has 119 other recalls on record since Oct. 22, 2021. Other recent recalls of similar products include Medline Convenience Kits Recall: Contaminated Components Risk (July 10, 2026), Medline Convenience Kits Recall: Sterile Packaging Risk (June 12, 2026), and Medline Convenience Kits Recall: Risk of Sterile Packaging Breach (June 12, 2026).
How to tell if you have this one
Check for model numbers DYNJAA254A or DYNJAA262A on the kits. The lot numbers 24KBR956, 24LBA655 for the first kit and 24LBD397 for the second kit are also indicators of affected units.
Brand
Medline
Category
Medical device
FDA recall event · 2 products
All 2 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
US States: CA, NY
Recall number
Product, codes & lots
Quantity
Z-1182-2025
Medline Convenience Kits for Various Procedures: 1) ADULT INTUBATION TRAY, Model Number DYNJAA254A; 2) ADULT MAIN DISP. INTUB PART A, Model Number DYNJAA262A; 1) DYNJAA254A, UDI-DI 10195327686260 (each) 40195327686261 (case), Lot Number 24KBR956, 24LBA655; 2) DYNJAA262A, UDI-DI 10195327208172 (each) 40195327208173 (case), Lot Number 24LBD397
70 kits
Z-1183-2025
Medline Convenience Kits for Various Procedures: 1) CLOVIS RESP/INTUB DRAWER 2, Model Number ACC010809; 2) RESP/INTUBATION DRAWER #2, Model Number ACC010813; 1) ACC010809, UDI-DI 10198459012235 (each) 40198459012236 (case), Lot Number 24JDC400; 2) ACC010813, UDI-DI 10198459012556 (each) 40198459012557 (case), Lot Number 24KDA437
0 kits
Based on the official FDA remedy
What to do — step by step
Check Kit Model Numbers
Look for model numbers DYNJAA254A or DYNJAA262A on the kits.
Where it went and when
Where it was distributed
Distributed in California and New York.
Listed by the agency
Not listed
FDA distribution: “US States: CA, NY” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, New York.
Recall timeline
FDA published this recall 48 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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-1182-2025 (January 9, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1182-2025 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.