Device recall
Z-0680-05: Sheridan Sher-I-Bronch Left Endobronchial Tube; an Rx, sterile, sinlge use…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-0680-05 |
|---|---|
| Recall event | 31205 |
| Product | Sheridan Sher-I-Bronch Left Endobronchial Tube; an Rx, sterile, sinlge use endobronchial tube with modified tip for left bronchial intubation, 37 Fr.; Hudson Respiratory Care Inc., Temecula, CA 92589-9020, Manufactured in Mexico; sold under the following catalog numbers: a) catalog number (REF)… |
| Product code | CBI |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 31, 2006 |
| 510(k) numbers | K851856 |
| FEI number | 3004959265 |
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