Device recall
Z-1683-2022: Medline CHEST TUBE REORDER NO: DYNJ36762A
FDA device recall · Class II · Medline Industries Inc.
Key facts
| Recall number (Z-number) | Z-1683-2022 |
|---|---|
| Recall event | 90689 |
| Product | Medline CHEST TUBE REORDER NO: DYNJ36762A |
| Product code | LRP |
| Recalling firm | Medline Industries Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3005595283 |
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