Device recall
Z-0040-2012: Prostrate Seeding Applicator Needle. Product code PSS1820AT Packed in boxes of…
FDA device recall · Class II · Worldwide Medical Technologies, LLC
Key facts
| Recall number (Z-number) | Z-0040-2012 |
|---|---|
| Recall event | 59712 |
| Product | Prostrate Seeding Applicator Needle. Product code PSS1820AT Packed in boxes of (25) with five Single Packs and four five packs or as singles or five packs. Worldwide Medical Technologies, LLC Used to introduce radionuclide seeds of 1-125 or Pd-103 into the body for radiation therapy. This device is… |
| Product code | IWJ |
| Recalling firm | Worldwide Medical Technologies, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 19, 2012 |
| FEI number | 3000206637 |
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