Device recall
Z-0374-06: Kimberly-Clark/Ballard TRACH CARE* - 72 Wet Pak* for Adults * Closed Suction…
FDA device recall · Class II · Kimberly-Clark Corporation
Key facts
| Recall number (Z-number) | Z-0374-06 |
|---|---|
| Recall event | 34218 |
| Product | Kimberly-Clark/Ballard TRACH CARE* - 72 Wet Pak* for Adults * Closed Suction System with Saline Vials * Diameter 14 Fr (4.6 mm), Length 30.5 cm (12 in) * Rx Only * Single Use * Manufactured by Ballard Medical Products, Draper, Utah 84020 USA, Distributed in the US by Kimberly-Clark Global Sales… |
| Product code | BSY |
| Recalling firm | Kimberly-Clark Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 6, 2006 |
| FEI number | 1000015879 |
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