Device recall
Z-2018-2010: Angiotech Vascular Access Needle. A) "Modified Potts/Cournand" Needle. STERILE…
FDA device recall · Class II · Medical Device Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-2018-2010 |
|---|---|
| Recall event | 54688 |
| Product | Angiotech Vascular Access Needle. A) "Modified Potts/Cournand" Needle. STERILE. Product Number: MPCN1802. 510k K974745. Qty Dist. - 425. B) "Seldinger" Needle. STERILE. Product Number: SN1802, SN1902. 510k K974745. Qty Dist. - 5,250. MEDICAL DEVICE TECHNOLOGIES, INC. 3600 Southwest 74th Avenue… |
| Product code | DRC |
| Recalling firm | Medical Device Technologies, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 25, 2011 |
| 510(k) numbers | K974745 |
| FEI number | 1036710 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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