FDAFDA recall Z-2417-2026 · Jun 24, 2026
Medline Industries, LP: MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-CATH DYNJ63276G recall
Recall found
Product
MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-CATH DYNJ63276G
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.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- DYNJ84775A UDI-DI 10195327606527 lot 25LMH070 DYNJ47269D UDI-DI 10195327674786 lot 25LMJ234 DYNJ63276G UDI-DI 10198459458835 lot 26BBC598
- Quantity
- 49,654 kits total
- Distribution
- US Nationwide distribution. OUS distribution pending.
- Recalling firm
- Medline Industries, LP, Northfield, IL
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-04-27
Source: openFDA enforcement record Z-2417-2026 · search recall number Z-2417-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.