Device recall
Z-0487-2015: Cannulaide, Model 101. The Cannulaide product is composed of die-cut…
FDA device recall · Class II · Beevers Manufacturing & Supply, Inc.
Key facts
| Recall number (Z-number) | Z-0487-2015 |
|---|---|
| Recall event | 69648 |
| Product | Cannulaide, Model 101. The Cannulaide product is composed of die-cut hydrocolloid coated polyurethane film with an integral hook strip (i.e., Velcro) to allow for the use of a loop material to help secure a nasal interface. The Cannulaide is applied under and over the nose of infants to provide a… |
| Product code | BZD |
| Recalling firm | Beevers Manufacturing & Supply, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 1, 2014 |
| FEI number | 3023468 |
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