Device recall
Z-2444-2024: Medline procedure kits labeled as: 1) WMC HYBRID OR PACK PART 1, Pack Number…
FDA device recall · Class I · MEDLINE INDUSTRIES, LP - Northfield
Key facts
| Recall number (Z-number) | Z-2444-2024 |
|---|---|
| Recall event | 94580 |
| Product | Medline procedure kits labeled as: 1) WMC HYBRID OR PACK PART 1 , Pack Number CMPJ08068F ; 2) VASCULAR PACK , Pack Number CMPJ11455B ; 3) SALEM CATH LAB-LF , Pack Number DYNJ26938J ; 4) EH PEDIATRIC CATH , Pack Number DYNJ49920L ; 5) ARTERIOGRAM PACK, Pack Number DYNJ53018; 6) CATH PACK , Pack… |
| Product code | OES |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 1417592 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database