Drug recall
Medline Kits: 1) ANGIO CATH PACK-MARY IMMACULAT, Model Number: DYNJ24517D
FDA recall event 98599 · Class II · Medline Industries, LP
Key facts
| Event ID | 98599 |
|---|---|
| Recall numbers | Z-1829-2026, Z-1830-2026, Z-1831-2026, Z-1832-2026, Z-1833-2026, Z-1834-2026, Z-1835-2026, Z-1836-2026, Z-1837-2026, Z-1838-2026, Z-1839-2026, Z-1840-2026 and 10 more |
| Recalling firm | Medline Industries, LP |
| Product type | Devices |
| Products | Medline Kits: 1) ANGIO CATH PACK-MARY IMMACULAT, Model Number: DYNJ24517D, Medline Kits: 1) ANGIOGRAPHY PACK-LF, Model Number: DYNJQ0505M; 2) ANGIO PACK, Model Number: DYNJT2021G; 3) ANGIOGRAPHY PACK, Model Number: DYNJ31377B; 4) ANGIO PACK, Model Number: DYNJ51279; 5)…, Medline Kits: 1) ARTHROGRAM TRAY, Model Number: DYNJ07425; 2) TOL NEURO ANGIO PACK, Model Number: DYNJ38610I 3) ANGIOGRAPHY PACK, Model Number: DYNJ45234A 4) C.I.C.N. ANGIO PACK, Model Number…, Medline Kits: 1) ARTHROSCOPY PACK, Model Number: DYNJ82440, Medline Kits: 1) BREAST PACK, Model Number: DYNJ66777D and 17 more |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. |
| Initiation date | Feb 25, 2026 |
| Report date | Apr 29, 2026 |
| City | Northfield |
| State | IL |
| Country | United States |
| FEI number | 1417592 |
At a glance
- 10–99 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: