Device recall
Z-0080-2012: "***Vipat REF H0020-100***Lot 100533***2015-04***STERILE EO Elastomeric…
FDA device recall · Class I · Victus, Inc.
Key facts
| Recall number (Z-number) | Z-0080-2012 |
|---|---|
| Recall event | 59984 |
| Product | "***Vipat REF H0020-100***Lot 100533***2015-04***STERILE EO Elastomeric pump***2mL/Hr***100mL***Medpro International (Thailand) Ltd. 360, Moo 6, Chonburi Industrial Estate, Tambon Bowin, Amphur Sriracha, Chonburi 20230, Thailand***Victus Inc. 4918 SW 74 Court 33155 44400***" Packed 24 units per… |
| Product code | MEB |
| Recalling firm | Victus, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jan 12, 2012 |
| FEI number | 3002843564 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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