Device recall
Z-0062-2019: Laparoscopy Instruments Instructions For Use (IFU) for the following…
FDA device recall · Class III · Dannoritzer Medizintechnik GmbH & Co. KG
Key facts
| Recall number (Z-number) | Z-0062-2019 |
|---|---|
| Recall event | 80970 |
| Product | Laparoscopy Instruments Instructions For Use (IFU) for the following: 1)Monopolar electrode, 2) Insert, handle and/or shaft component of a modular forceps or scissors for electrosurgical coagulation, 3) One-piece forceps or scissors for electrosurgical coagulation |
| Product code | GEI |
| Recalling firm | Dannoritzer Medizintechnik GmbH & Co. KG |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 22, 2019 |
| 510(k) numbers | K052759 |
| FEI number | 1000482681 |
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