Device recall
Z-0278-2023: PAJUNK Continuous Epidural Tray, Tuohy Epidural Needle 17G x 4" with EpiLong…
FDA device recall · Class II · Pajunk Medical Systems, L.P.
Key facts
| Recall number (Z-number) | Z-0278-2023 |
|---|---|
| Recall event | 91037 |
| Product | PAJUNK Continuous Epidural Tray, Tuohy Epidural Needle 17G x 4" with EpiLong Soft Catheter, Closed Tip, 19G, Model #TAL101, sterile, each tray contains 5ml Ampule 1% Lidocaine HCl, 10ml Ampule 0.9% Sodium Chloride, and 5ml Ampule 1.5% Lidocaine HCl with Epinephrine 1:200,000. |
| Product code | OGE |
| Recalling firm | Pajunk Medical Systems, L.P. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 17, 2024 |
| FEI number | 3004076349 |
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