Device recall
Z-0307-2009: Uni-CP Compression Forceps (spreader); Non-sterile, R only, Catalog number…
FDA device recall · Class II · Integra LifeSciences Corp
Key facts
| Recall number (Z-number) | Z-0307-2009 |
|---|---|
| Recall event | 49561 |
| Product | Uni-CP Compression Forceps (spreader); Non-sterile, R only, Catalog number: 339001ND Newdeal, Lyon, France; Integra, 411 Enterprise Drive, Plainsboro, NJ 08536 Intended to open the UNI-Compression Plate olive, which creates a compression. |
| Product code | HRS |
| Recalling firm | Integra LifeSciences Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 11, 2009 |
| 510(k) numbers | K070447 |
| FEI number | 1121308 |
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