Medline Industries IV administration and extension sets recalled for connector leaks
What this means
Medline Industries is recalling 23 models of IV administration and extension sets because the male connectors may leak, crack, or break during use under certain conditions. This could cause delays in treatment, blood loss, infection, air embolism, or patients not receiving the correct medication dose.
- Check if your facility uses any Medline IV sets with model numbers starting with DYNDTB (such as DYNDTB0529, DYNDTB1029, DYNDTB1516, or others listed in the recall)
- Stop using affected sets immediately
- Contact Medline Industries or your supplier for replacement sets
- Report any injuries or problems to the FDA's MedWatch program at 1-888-SAFEMEDS
The agency's original wording
Under circumstances involving exposure to particular chemicals and mechanical forces, the male luer connectors for the specified IV Administration and Extension sets may leak, crack, and/or break during use, which may result in a delay in patient treatment, blood loss, infection, an air embolism, and/or underdosage of medication.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1366-2026More Medline recalls
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- FDA-Device2026-09-09Medline Convenience Kits with BD ChloraPrep Clear applicators recalled for contamination risk
- FDA-Device2026-09-09Medline Convenience Kits recalled for sterility packaging breach risk
- FDA-Device2026-09-09Medline Convenience Kits with BD ChloraPrep Clear applicators recalled for defective packaging seals
- FDA-Device2026-09-09Medline Arterial Line Insertion Kit recalled for sterility packaging breach risk
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