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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 Adult Anesthesia Sets Recalled Due to Leaking IV Components

Agency Publication Date: October 10, 2025
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Summary

Medline Industries, LP is recalling 950 units of the Medline Adult Anesthesia Set (REF DYNJ39985G) because they may contain components from a separate recall. These kits include Clearlink IV Sets that were previously recalled by Baxter due to reports of leaking. The specific Medline kit affected by this recall is lot number 25GMB464.

Risk

Leaking IV sets can result in patients receiving an incorrect dose of fluid or medication, or may allow air to enter the infusion line. These defects were identified following customer reports of leaking components.

What You Should Do

  1. This recall affects the Medline Adult Anesthesia Set (REF DYNJ39985G) from lot number 25GMB464, which contains recalled Clearlink IV components.
  2. Check your product labeling for the catalog number REF DYNJ39985G and lot number 25GMB464 to determine if your kit is affected. You can also identify the product by UDI/DI 10198459062353 (individual units) or 40198459062354 (cases).
  3. Stop using the recalled product immediately.
  4. Contact Medline Industries, LP or your distributor to arrange for the return, replacement, or correction of the affected anesthesia sets.
  5. Call the FDA Consumer Complaint hotline at 1-888-463-6332 (1-888-INFO-FDA) for additional questions.

Your Remedy Options

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

Affected Products

Product: Medline Adult Anesthesia Set
Model / REF:
DYNJ39985G
Lot Numbers:
25GMB464
UDI:
10198459062353
40198459062354

Product contains Clearlink IV Sets which Baxter recalled due to customer reports of leaking.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97650
Status: Active
Manufacturer: Medline Industries, LP
Sold By: Authorized medical distributors
Manufactured In: United States
Units Affected: 950 units
Distributed To: Missouri

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.