Medline Arterial Line Pack Recalled: Mislabeling Risk in Medical Kits
Medline recalls arterial line packs with mislabeled heparin-coated catheters that could be distributed in medical kits. Affected lots include 24IMA276, 24JMI065, 24FMF777, 24GMG420.
Lower-risk recall
Certain lots Sterile Infusion Catheters which were mislabeled as having a heparin coating were either distributed or manufactured into medical convenience kits and distributed.
Contact the company
What happened, in plain English
Medline is recalling arterial line packs that were mislabeled as having heparin coating. This could lead to improper use in medical settings if the catheters are used without the correct coating. Read more at govinfonow.com/recall/53170-medline-arterial-line-pack-recalled-mislabeling-risk-in-medical-kits.
Source Summary by GovInfoNow · govinfonow.com/recall/53170-medline-arterial-line-pack-recalled-mislabeling-risk-in-medical-kits · Updated August 18, 2026 · FDA enforcement record: FDA #Z-1049-2025
Cite this page
“Medline Arterial Line Pack Recalled: Mislabeling Risk in Medical Kits.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/53170-medline-arterial-line-pack-recalled-mislabeling-risk-in-medical-kits. Based on FDA recall #Z-1049-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1049-2025%22&limit=1).
Why it’s dangerous
The catheters were mislabeled as having heparin coating but were actually distributed without it. This could cause improper anticoagulation during medical procedures, potentially leading to clotting issues.
Who’s affected
Healthcare providers using Medline arterial line packs with specific lot numbers are most at risk. Patients receiving care with these kits may also be affected.
How to tell if you have this one
Check for lot numbers 24IMA276, 24JMI065, 24FMF777, or 24GMG420 on the Medline Arterial Line Pack (REF DYNJ65208B).
- Brand
Medline- Category
Medical device
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: FL, KS, ND, PA, WA, WV, IL, WA
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-1048-2025 | CENTURION Infusion Catheter, 7F, 17cm (DO), Reorder MIC17F7; Infusion Catheter with Antimicrobial Heparin Coating.; UDI/DI 10653160249979 (EA) 20653160249976 (CS), Lot Numbers: 2024103190, 2024050990, 2024021290, 2024012990, 2024111990 | 1200 units |
| Z-1049-2025 | MEDLINE ARTERIAL LINE PACK, REF DYNJ65208B, medical convenience kit containing Infusion Catheter with Antimicrobial Heparin Coating.; UDI/DI 10195327561543 (ea) 40195327561544 (cs), Lot Numbers: 24IMA276, 24JMI065, 24FMF777, 24GMG420 | 50 units |
What to do — step by step
Check Lot Numbers
Look for lot numbers 24IMA276, 24JMI065, 24FMF777, or 24GMG420 on the product label.
Where it went and when
Where it was distributed
Distributed in 7 states.
FDA distribution: “US: FL, KS, ND, PA, WA, WV, IL, WA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida, Illinois, Kansas, North Dakota, Pennsylvania, Washington, West Virginia.
Recall timeline
FDA published this recall 44 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
Is there a risk of serious injury?
The recall addresses a potential risk of improper anticoagulation, but the hazard level is low risk as the remedy focuses on checking labels rather than immediate action.
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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-1049-2025 (December 23, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1049-2025 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.