Device recall
Z-3107-2026: Kit: Single Shot Epidural 20/Cs, REF: 59553; Kit: Single Shot Epidural 20/Cs…
FDA device recall · Class I · Medical Action Industries, Inc. 306
Key facts
| Recall number (Z-number) | Z-3107-2026 |
|---|---|
| Recall event | 99613 |
| Product | Kit: Single Shot Epidural 20/Cs, REF: 59553; Kit: Single Shot Epidural 20/Cs, REF: 83945B. Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules |
| Product code | OFT |
| Recalling firm | Medical Action Industries, Inc. 306 |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 1030451 |
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