Device recall
Z-0172-2012: Shoulder Flex Massage Device Device is an electric personal massage device…
FDA device recall · Class I · King International
Key facts
| Recall number (Z-number) | Z-0172-2012 |
|---|---|
| Recall event | 59829 |
| Product | Shoulder Flex Massage Device Device is an electric personal massage device labeled in part: "ShoulderFlex Deep-kneading Shiatsu* Model #SH61 *Read all instructions before using the massager* **WARNING NEVER wear a necklace or similar items while using this product Made in China." Personal use… |
| Product code | ISA |
| Recalling firm | King International |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 6, 2014 |
| FEI number | 3004168104 |
At a glance
- None 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