Custom Interventional Pain Management recalls
Custom Interventional Pain Management appears in 1 official U.S. recall notice indexed by RecallRadar, most recently on 2026-10-07.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 1 |
|---|---|
| Published | 2026-10-07 |
| By agency | FDA Device (1) |
| By classification | Class II (1) |
| By status | ongoing (1) |
| Distribution named in notices | US |
Recalls
- Brand Name: Ferndale Laboratories
FDA Device · Class II · 2026-10-07 · Custom Interventional Pain Management
Reason: Due to manufacturing issues with the liquid skin adhesive containing in surgical convenience trays/kits.