Device recall
Z-0595-2016: MED-RX Single Use REF 54-3680R, 8 FR. x 36" (91CM) Polyurethane Feeding Tube For…
FDA device recall · Class II · Benlan, Inc.
Key facts
| Recall number (Z-number) | Z-0595-2016 |
|---|---|
| Recall event | 72851 |
| Product | MED-RX Single Use REF 54-3680R, 8 FR. x 36" (91CM) Polyurethane Feeding Tube For Pediatric Use with Orange Radiopaque Stripe and Enteral Connector, Made in Canada, Benton, Oakville, Ontario, Canada |
| Product code | FPD |
| Recalling firm | Benlan, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 31, 2016 |
| 510(k) numbers | K100700 |
| FEI number | 3932 |
At a glance
- 1–9 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