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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

Centurion Catheters and Arterial Line Packs Recalled for Mislabeled Coating

Agency Publication Date: January 29, 2025
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Summary

Medline Industries, LP is recalling Centurion Infusion Catheters and Medline Arterial Line Packs because they were mislabeled as having an antimicrobial heparin coating when they do not. Approximately 1,250 units are affected by this recall, including 1,200 infusion catheters and 50 arterial line convenience kits. These products were distributed to hospitals and medical facilities in several states including Florida, Illinois, Kansas, North Dakota, Pennsylvania, Washington, and West Virginia.

Risk

Patients may be at a higher risk for blood clots or infections if a medical provider uses a catheter that lacks the antimicrobial heparin coating they believe is present. While no injuries or incidents have been reported to date, the lack of expected protective coating could lead to serious medical complications during clinical procedures.

What You Should Do

  1. This recall affects Centurion Infusion Catheters (Model MIC17F7) and Medline Arterial Line Packs (Model DYNJ65208B) that were distributed or manufactured into medical convenience kits and mislabeled as having an antimicrobial heparin coating.
  2. Identify if you have the affected catheters by checking for lot numbers 2024103190, 2024050990, 2024021290, 2024012990, or 2024111990 on the packaging.
  3. Identify if you have the affected arterial line packs by checking for lot numbers 24IMA276, 24JMI065, 24FMF777, or 24GMG420 on the packaging.
  4. Stop using the recalled catheters and kits immediately and remove them from your clinical inventory.
  5. Contact Medline Industries, LP or your medical supply distributor to arrange for the return, replacement, or correction of the affected units.
  6. Call the FDA Consumer Complaint hotline at 1-888-463-6332 (1-888-INFO-FDA) 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: CENTURION Infusion Catheter, 7F, 17cm (DO)
Model / REF:
MIC17F7
Lot Numbers:
2024103190
2024050990
2024021290
2024012990
2024111990
UDI:
10653160249979
20653160249976

Mislabeled as having Antimicrobial Heparin Coating.

Product: MEDLINE ARTERIAL LINE PACK
Model / REF:
DYNJ65208B
Lot Numbers:
24IMA276
24JMI065
24FMF777
24GMG420
UDI:
10195327561543
40195327561544

Medical convenience kit containing mislabeled Infusion Catheter.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96066
Status: Active
Manufacturer: MEDLINE INDUSTRIES, LP - Northfield
Sold By: Medical facilities; Hospitals
Manufactured In: United States
Units Affected: 2 products (1200 units; 50 units)
Distributed To: Florida, Kansas, North Dakota, Pennsylvania, Washington, West Virginia, Illinois

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.