Medline medical procedure kits recalled for catheter defects
Medline procedure kits recalled for catheter defects
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.
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-PR2026-08-05Medline Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits recalled for connector overheating risk
- FDA-Device2026-07-29Medline surgical convenience kits recalled for quality issues in anesthetic component
- FDA-Device2026-07-29Medline NEURO PACK medical kits recalled for Bacillus contamination
- FDA-Device2026-07-29Medline convenience kits with Bard Silastic Foley Catheters recalled for surface contamination
- FDA-Device2026-07-29Medline convenience kits with Bard Silastic Foley Catheters recalled for surface contamination
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