Device recall
Z-2587-2017: Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-2587-2017 |
|---|---|
| Recall event | 77330 |
| Product | Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets manufactured from galvanized carbon steel and aluminum rods that are coated with a blue PVC or polypropylene outer covering and are designed to be placed inside an endotracheal tube to obtain a desired shape during… |
| Product code | BSR |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3005747797 |
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