Device recall
Z-0266-2012: Rapid Strand Rx; the RAPID Strand Rx kit consists of custom loaded absorbable…
FDA device recall · Class II · Medi-Physics Inc. dba GE Healthcare
Key facts
| Recall number (Z-number) | Z-0266-2012 |
|---|---|
| Recall event | 60005 |
| Product | Rapid Strand Rx; the RAPID Strand Rx kit consists of custom loaded absorbable seeding spacers and I-125 radionuclide brachytherapy sources (seeds) spaced at prescribed distance and configuration within a sleeve (tube) made of absorbable suture material, stiffened, loaded into prostate seeding… |
| Product code | KXK |
| Recalling firm | Medi-Physics Inc. dba GE Healthcare |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 20, 2012 |
| 510(k) numbers | K063177 |
| FEI number | 1417338 |
At a glance
- 1–9 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