Device recall
Z-0058-2017: Teleflex Percuaneous Solutions, Gripper Grasper, Ref ML003EE, Rx Only Sterile…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-0058-2017 |
|---|---|
| Recall event | 75130 |
| Product | Teleflex Percuaneous Solutions, Gripper Grasper, Ref ML003EE, Rx Only Sterile Manufactured for: Teleflex Medical, Park, NC 27709 The Percutaneous Surgical System with 5 mm attachments is indicated for the means to penetrate soft tissue to access certain areas of the human abdomen and used to grasp… |
| Product code | GCJ |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 25, 2017 |
| 510(k) numbers | K143299 |
| FEI number | 3005747797 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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