Device recall
Z-1470-2022: Medline Convenience kits labeled as follows: a. BEDSIDE PICC CDS, Model Number…
FDA device recall · Class II · MEDLINE INDUSTRIES, LP - SPT
Key facts
| Recall number (Z-number) | Z-1470-2022 |
|---|---|
| Recall event | 90516 |
| Product | Medline Convenience kits labeled as follows: a. BEDSIDE PICC CDS, Model Number CDS984642, b. VASCULAR CDS, Model Number DYNJ902880J, c. VASCULAR CDS, Model Number DYNJ902880K, d. OPEN HEART A & B, Model Number DYNJ904831F, e. OPEN HEART MHS, Model Number DYNJ905394A, f. OPEN HEART MHS, Model Number… |
| Product code | OEZ |
| Recalling firm | MEDLINE INDUSTRIES, LP - SPT |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3000717925 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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