Device recall
Z-0169-2009: Alpha-Omega Services, Inc. Product No:NFW0001-009 Description: FLEXIGUIDE…
FDA device recall · Class II · Alpha Omega Services Inc
Key facts
| Recall number (Z-number) | Z-0169-2009 |
|---|---|
| Recall event | 49128 |
| Product | Alpha-Omega Services, Inc. Product No:NFW0001-009 Description: FLEXIGUIDE NEEDLE, SERIES-15, 20 CM WITHOUT FEMALE LUER ADAPTOR, SHARP AND STYLET WITH 90-DEGREE BEND, 10/PKG Quantity: 10/PKG L-NFW0001-009. The FlexiGuide is a flexible needle designed to provide an enclosed pathway for localized… |
| Product code | IWJ |
| Recalling firm | Alpha Omega Services Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 9, 2008 |
| FEI number | 2022694 |
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