Beeken Biomedical recalls
Beeken Biomedical appears in 1 official U.S. recall notice indexed by RecallRadar, most recently on 2021-12-08.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 1 |
|---|---|
| Published | 2021-12-08 |
| By agency | FDA Device (1) |
| By classification | Class II (1) |
| By status | ongoing (1) |
| Distribution named in notices | MO |
Recalls
- NuStat 8" x12" Trauma Pad XR Hemafiber, 5-pack
FDA Device · Class II · 2021-12-08 · Beeken Biomedical
Reason: Endotoxin levels exceeded allowable limits.