Device recall
Z-2835-2026: Charger for the Therabody Theragun, G4 PRO massage device, and products which…
FDA device recall · Class II · Therabody, Inc
Key facts
| Recall number (Z-number) | Z-2835-2026 |
|---|---|
| Recall event | 99281 |
| Product | Charger for the Therabody Theragun, G4 PRO massage device, and products which include the 4th Generation Theragun PRO charger. G4 PRO Black US - Refurb., SKU TG02428-01 G4 PRO NA, SKU G4-PRO-PKG-NA G4-PRO-PKG-US, SKU G4 PRO US G4 PRO Black US - Refurb V, SKU TG0002428-1V10 Pro Charger Single Unit… |
| Product code | ISA |
| Recalling firm | Therabody, Inc |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3012386142 |
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