FDA recall notice
Epidural Kit Correction: Medical Action Industries Issues Correction for Epidural Kits…
FDA Recall Confirmed · Epidural Kit · posted Sep 10, 2026
Key facts
| Notice | Epidural Kit Correction: Medical Action Industries Issues Correction for Epidural Kits Containing Spectra Medical Devices Lidocaine Ampules |
|---|---|
| Device type | Epidural Kit |
| Status | Recall Confirmed |
| Posted | Sep 10, 2026 |
| Notice on fda.gov | fda.gov |
At a glance
- Confirmed Recall confirmed
- Yes Currently listed by the FDA
- 1–9 Recall events referenced
- 1–9 UDI device identifiers named
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recall notices and early alerts
The FDA's Medical Device Recalls and Early Alerts list covers the most serious device recalls, plus early alerts about potentially high-risk device issues while the FDA is still collecting information. A notice is updated as the recall is confirmed or changes.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls and Early Alerts · Source date: