Device recall
Z-0655-2017: SURESOUND22US Multipack (US Distribution) containing 2 packs of six devices…
FDA device recall · Class II · Hologic, Inc
Key facts
| Recall number (Z-number) | Z-0655-2017 |
|---|---|
| Recall event | 75558 |
| Product | SURESOUND22US Multipack (US Distribution) containing 2 packs of six devices. SURESOUND22 Multipack (OUS Distribution) containing 2 packs of six devices. For uterine sound |
| Product code | HHM |
| Recalling firm | Hologic, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 18, 2017 |
| FEI number | 1000120743 |
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