Arrowhead DE LLC
1
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Medical Device
2026-08-26 to 2026-08-26
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-08-26 | FDA Device | FDA Recall: Arrow-LOK Implant, REF: 21-253519, 21-253522, 21-253525, 21-253528, 21-253530, 21-253533, 21- | Arrowhead DE LLC | Class II | N/A |