Device recall
Z-0068-2012: STRIP T's STERILE ADHESIVE ORGANIZER, Model #SC5000-4R, Lot #090710, 510(k)…
FDA device recall · Class III · Kapp Surgical Instrument Inc
Key facts
| Recall number (Z-number) | Z-0068-2012 |
|---|---|
| Recall event | 60000 |
| Product | STRIP T's STERILE ADHESIVE ORGANIZER, Model #SC5000-4R, Lot #090710, 510(k) exempt. One (1) adhesive organizer is packed in a Tyvek pouch and 60 pouches are placed into a 'Shelf Box'. The shelf box is placed into a shipping container. The Sterile Adhesive Organizer is used to hold tubing or… |
| Product code | KGT |
| Recalling firm | Kapp Surgical Instrument Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Feb 19, 2013 |
| FEI number | 1522875 |
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