FDA-Device2026-01-21Class IIPROCESSING DEFECT
Medline Neuro Angio Pack IV administration kits recalled for stuck check valves
What this means
Medline kits containing B. Braun IV administration sets have been recalled because the check valve components may become stuck in either the open or closed position. This could affect proper fluid delivery through the IV line. The affected kits are labeled as Neuro Angio Pack with SKU DYNJ38935, lot number 25IBC144.
- Stop using any Medline Neuro Angio Pack IV administration kits (SKU DYNJ38935, lot 25IBC144)
- Contact your healthcare facility or Medline for instructions on replacement or disposal
- Do not use these kits for patient care
The agency's original wording
Hazard
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.
Intended for
Adults
Illnesses reported
None reported
Sold states
US Nationwide distribution.
Affected count
12 units
Manufactured in
3 Lakes Dr, Northfield, IL, United States
Products
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: NEURO ANGIO PACK, Medline kit SKU DYNJ38935
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1059-2026More Medline recalls
- FDA-Device2026-09-09Medline Convenience Kits recalled for potential sterility breach in antiseptic applicators
- 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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