Device recall
Z-1159-2020: Button-Style Tocotransducer (Nautilus), 8-foot Cord 2264HAX, that may have been…
FDA device recall · Class II · Pacific Medical Group Inc.
Key facts
| Recall number (Z-number) | Z-1159-2020 |
|---|---|
| Recall event | 83610 |
| Product | Button-Style Tocotransducer (Nautilus), 8-foot Cord 2264HAX, that may have been serviced with the following: Pacific Medical GE Corometrics Nautilus Toco Board, NFCM9310; Pacific Medical GE Corometrics Nautilus TOCO Bottom Case, NFCM9315; Pacific Medical GE Corometrics Nautilus TOCO Cable Assembly… |
| Product code | HFM |
| 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