Medline medical procedure kits recalled for catheter defects
What this means
Medline identified that samples of multiple surgical procedure kits did not meet performance standards. The kits contained catheters with surface irregularities, connectors that detached prematurely, and diameter measurements that fell outside specifications.
- Check if your facility uses any of the affected Medline kit models (50 different procedure kits, including laparoscopy, ECMO, and gynecology packs).
- Review the lot numbers and SKU numbers provided in the recall notice against your inventory.
- Contact Medline Industries for instructions on returning or replacing affected kits.
The agency's original wording
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2493-2026More 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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