FDAHealthFebruary 25, 2026
Medline Industries, LP — Medline Kits: 1) ANGIO CATH PACK-MARY IMMACULAT, Model Number: DYNJ24517D
⚠️ The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Is this relevant to me?
- Geography
- Nationwide
- Source agency
- FDA
- Category
- Health
- Published
- February 25, 2026
US Nationwide distribution.
What's affected?
- Product
- Medline Kits: 1) ANGIO CATH PACK-MARY IMMACULAT, Model Number: DYNJ24517D
- Lot code
- 25CBA224
Additional details
1) DYNJ24517D, UDI-DI: 10193489812510(each), 40193489812511(case), Lot Number: 25CBA224
What should I do?
Recommended action
Class II recall. Voluntary: Firm initiated Quantity affected: 15 units.
Get Health recall alerts
Delivered to your inbox. Free. No account required.