Medline Industries IV administration and extension sets recalled for connector leaks
Stop using Medline IV administration sets
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
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 Industries, LP recalls
- FDA-Device2026-06-03Medline EYE TRAY-LF medical kit recalled for mismatched syringes
- FDA-Device2026-06-03Medline spinal anesthesia and nerve block kits recalled for bupivacaine quality and efficacy concerns
- FDA-Device2026-05-20Medline Namic Preceptor blood pressure manifold recalled for particulate contamination
- FDA-Device2026-05-20Medline TAVI medical convenience kits recalled for particulate contamination in fluid path
- FDA-Device2026-05-20Medline medical convenience kits with Namic Manifold recalled for particulate contamination
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