Device recall
Z-0181-04: Otto Bock Kimba Plus Pediatric Tilt-in-Space Postural Mobility Systems…
FDA device recall · Class II · Bock,Otto,Orthopedic Ind,Inc
Key facts
| Recall number (Z-number) | Z-0181-04 |
|---|---|
| Recall event | 27588 |
| Product | Otto Bock Kimba Plus Pediatric Tilt-in-Space Postural Mobility Systems (Strollers), Product Numbers HR32571001-012, HRK3269=06-027_X, R32651001-012, HRK3283=01-026_X, HRK3269=01-026_X, HRK3283=02-026_X, HRK3269=02-026_X, HRK3283=03-027_X, HRK3269=03-027_X, HRK3283=04-027_X, HRK3269=04-027_X… |
| Product code | IOR |
| Recalling firm | Bock,Otto,Orthopedic Ind,Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 7, 2005 |
| FEI number | 2182293 |
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