Device recall
Z-2111-2019: 1 pc Full Wrap Support Belt Apron, Product Number F111, Part Numbers MTREF111*F…
FDA device recall · Class II · Burlington Medical, LLC
Key facts
| Recall number (Z-number) | Z-2111-2019 |
|---|---|
| Recall event | 83144 |
| Product | 1 pc Full Wrap Support Belt Apron, Product Number F111, Part Numbers MTREF111*F, MTREF111E, MTREF111F, REF111*F, REF111*M, REF111B, REF111E, REF111F, SEF111*F, SEF111*M, SEF111C, SEF111D, SEF111E, SEF111F, UEF111*F, UEF111*M, UEF111A, UEF111B, UEF111C, UEF111D, UEF111E, UEF111XLM, UEF111XXLM Product… |
| Product code | EAJ |
| Recalling firm | Burlington Medical, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 28, 2023 |
| FEI number | 1000120804 |
At a glance
- None Linked 510(k)s
- 10–99 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