Device recall
Z-1471-2022: Medline convenience kits: a. VENOUS ACCESS PACK-LF, Model Number DYNJ36725B, Lot…
FDA device recall · Class II · MEDLINE INDUSTRIES, LP - SPT
Key facts
| Recall number (Z-number) | Z-1471-2022 |
|---|---|
| Recall event | 90516 |
| Product | Medline convenience kits: a. VENOUS ACCESS PACK-LF, Model Number DYNJ36725B, Lot codes: 19UBB149, b. KIT LB SHUNT, Model NumberDYNJ905860A, Lot codes: 22OBG246, 21LBU048, 21GBI196, 21KBK242, 21EBH567 Model/Catalog Number: a. Model Number DYNJ36725B, b. Model Number DYNJ905860A |
| Product code | OFF |
| 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
- 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