Device recall
Z-1568-05: Bard * Davol Reliavac 400 Closed Wound Suction Kit * Sterile/EO * Single use *…
FDA device recall · Class III · C.R. Bard, Inc., Urological Division
Key facts
| Recall number (Z-number) | Z-1568-05 |
|---|---|
| Recall event | 33284 |
| Product | Bard * Davol Reliavac 400 Closed Wound Suction Kit * Sterile/EO * Single use * Medium-Large 3/16'' (15 Fr., 4.7mm) O.D. PVC Drain * 12.5'' (31.7cm) Hole Pattern, X-ray Opaque Stripe Attached Trocar * 400cc Evacuator ** Y-Connecting Tube * * C.R. Bard Inc., Covington, GA 30014. The product contains a… |
| Product code | GBX |
| Recalling firm | C.R. Bard, Inc., Urological Division |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 21, 2009 |
| FEI number | 1018233 |
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