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RecallWatchMedical Device Safety
Class IIOngoingZ-2417-2026

Medline Industries, LP recalls MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-CATH D…

Medline Industries, LPNorthfield, IL, United StatesReported Jun 24, 2026 · 24 days ago
Legal News Analyst ·

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Affected product

Check your device

Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.

Affected products & lots

  • MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-CATHDYNJ63276G
    UDI-DI 10195327606527
    7 affected lots
    25LMH070DYNJ47269D1019532767478625LMJ234DYNJ63276G1019845945883526BBC598

What the firm is doing

Firm began notifying consignees on 4/27/2026. Customers were instructed to request stickers to over-label affected convenience kits with a warning label. Warning label indicates for user to remove the affected component and replace it with product from supply. No kits are to be returned.

DistributionShow details

US Nationwide distribution. OUS distribution pending.

Class IIWhat this means

Use of the product may cause temporary or medically reversible adverse health consequences.

Sources & references

Taylor Coteus
Legal News Analyst

Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.

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