Device recall
Z-1334-2021: CF Delivery Dev Caps Bravo x5, FGS-0635/FGS 0636 - Product Usage: intended to be…
FDA device recall · Class II · Covidien Llc
Key facts
| Recall number (Z-number) | Z-1334-2021 |
|---|---|
| Recall event | 87396 |
| Product | CF Delivery Dev Caps Bravo x5, FGS-0635/FGS 0636 - Product Usage: intended to be used for gastroesophageal pH measurement and monitoring of gastric reflux in adults and children from 4 years of age. |
| Product code | FFT |
| Recalling firm | Covidien Llc |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K102543 |
| FEI number | 1282497 |
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