Device recall
Z-0675-2017: ARROW OnControl Bone Marrow Biopsy System Tray, Sterile, Rx only, Manufactured…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-0675-2017 |
|---|---|
| Recall event | 75637 |
| Product | ARROW OnControl Bone Marrow Biopsy System Tray, Sterile, Rx only, Manufactured for: Teleflex Medical, The Arrow OnControl Bone Marrow Aspiration System is intended for bone marrow aspiration of the iliac crest of adult and pediatric patients. The Arrow OnControl Bone Marrow Biopsy System is intended… |
| Product code | KNW |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 20, 2019 |
| 510(k) numbers | K142377 |
| FEI number | 3005747797 |
At a glance
- 1–9 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