Device recall
Z-2282-2025: Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy…
FDA device recall · Class II · Carefree Surgical Specialties
Key facts
| Recall number (Z-number) | Z-2282-2025 |
|---|---|
| Recall event | 97259 |
| Product | Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner Rolls Gauze Medium 4 Long X-Ray Detectable 5/pk 25pk/CS Model/Catalog Number: 15505/25 Product Description: Robotic/Laparoscopy Kittner Rolls Gauze Medium 4 Long X-Ray Detectable 5/pk 25pk/CS |
| Product code | GDY |
| Recalling firm | Carefree Surgical Specialties |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K882708 |
| FEI number | 1000221450 |
At a glance
- 1–9 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