FDA-Device2026-06-24Class IIPROCESSING DEFECT
Medline catheter lab and vascular angio kits recalled for defective adhesive tubing
OTHERNationwide distribution
Medline catheter kits recalled for defective adhesive tubing
Medline Industries' Minor Cath Lab Pack, Vascular Angio Pack, and Port-a-Cath kits contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive. The adhesive's butyrate tubing may crack when used, making the kits unusable for their intended medical application.
- Check your kit lot number against the affected lots: 25LMH070 (Cath Lab), 25LMJ234 (Vascular Angio), or 26BBC598 (Port-a-Cath).
- If you have an affected kit, do not use it and contact Medline or your supplier for a replacement.
Hazard
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Sold states
US Nationwide distribution. OUS distribution pending.
Affected count
49,654 kits total
Manufactured in
3 Lakes Dr, Northfield, IL, United States
Products
MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-CATH DYNJ63276G
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2417-2026More Medline Industries, LP recalls
- FDA-Device2026-06-24Medline medical procedure kits recalled for catheter defects and connector detachment risk
- FDA-Device2026-06-24Medline cardiac surgery kits recalled for catheter defects
- FDA-Device2026-06-24Medline dressing change kits recalled for defective adhesive tubing
- FDA-Device2026-06-24Medline open-heart and cardiac surgery kits recalled for catheter defects
- FDA-Device2026-06-24Medline laparoscopy procedure kits recalled for catheter defects
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