Device recall
Z-1331-2013: DePuy LifeLiner Stick & Cut Resistant Gloves Rt, Lg Part No. 5200-68-000 The…
FDA device recall · Class III · DePuy Orthopaedics, Inc.
Key facts
| Recall number (Z-number) | Z-1331-2013 |
|---|---|
| Recall event | 65078 |
| Product | DePuy LifeLiner Stick & Cut Resistant Gloves Rt, Lg Part No. 5200-68-000 The gloves are designed to resist sticks and cuts and are not cut or puncture proof. These gloves are not required by any surgical technique. |
| Product code | FYE |
| Recalling firm | DePuy Orthopaedics, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jan 14, 2014 |
| FEI number | 1818910 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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