Device recall
Z-1162-2020: Loop-Style Ultrasound Transducer (Nautilus), 8-foot Cord 5700LAX, that may have…
FDA device recall · Class II · Pacific Medical Group Inc.
Key facts
| Recall number (Z-number) | Z-1162-2020 |
|---|---|
| Recall event | 83610 |
| Product | Loop-Style Ultrasound Transducer (Nautilus), 8-foot Cord 5700LAX, that may have been serviced with the following: Pacific Medical GE Corometrics Nautilus Ultrasound Board, NFCM9510; Pacific Medical GE Corometrics Nautilus Ultrasound Bottom Case, NFCM9515, Pacific Medical GE Corometrics Nautilus… |
| Product code | HGL |
| Recalling firm | Pacific Medical Group Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K012718 |
| FEI number | 3007409280 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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