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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Surgical Equipment

Medline Convenience Kits Recalled for Reduced Skin Barrier Adhesion

Agency Publication Date: February 19, 2025
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Summary

Medline Industries, LP is recalling 70 Medline Convenience Kits, including Adult Intubation Trays and Respiratory/Intubation Drawers. The recall was initiated because certain components within the kits have reduced skin barrier adhesion, causing the barriers to wear for a shorter time than expected before needing replacement. No incidents or injuries have been reported to date. These kits were distributed to hospitals and medical facilities in California and New York.

Risk

The skin barrier component in these kits may fail to properly adhere to or protect the skin for the intended duration. If the barrier fails or detaches early, it could lead to skin irritation or damage and requires more frequent replacement of medical components.

What You Should Do

  1. This recall affects Medline Convenience Kits, specifically Adult Intubation Trays (Models DYNJAA254A and DYNJAA262A) and Respiratory Intubation Drawers (Models ACC010809 and ACC010813).
  2. Check the lot number and UDI-DI printed on your product packaging or case label to see if it is affected. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled kits immediately.
  4. Contact Medline Industries, LP or your distributor to arrange for the return, replacement, or correction of the affected products.
  5. Call the FDA at 1-888-INFO-FDA (1-888-463-6332) for additional questions regarding this recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Medline Adult Intubation Tray and Adult Main Disposable Intubation Kits
Model / REF:
DYNJAA254A
DYNJAA262A
Lot Numbers:
24KBR956
24LBA655
24LBD397
UDI:
10195327686260
40195327686261
10195327208172
40195327208173

Quantity: 70 kits. Recall #: Z-1182-2025.

Product: Medline Clovis Respiratory/Intub Drawer 2 and Respiratory/Intubation Drawer #2
Model / REF:
ACC010809
ACC010813
Lot Numbers:
24JDC400
24KDA437
UDI:
10198459012235
40198459012236
10198459012556
40198459012557

Quantity: 0 kits. Recall #: Z-1183-2025.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96188
Status: Active
Manufacturer: MEDLINE INDUSTRIES, LP - Northfield
Sold By: Medline Industries; Hospitals; Medical facilities
Manufactured In: United States
Units Affected: 2 products (70 kits; 0 kits)
Distributed To: California, New York

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.