Johnson & Johnson Surgical Vision, Inc.
1
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Medical Device
2026-09-09 to 2026-09-09
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-09-09 | FDA Device | FDA Recall: HEALON EndoCoat PRO, REF: 10300012 (US/CAN) HEALON DUET PRO II, REF: 10300016 (US/CAN) HEALON E | Johnson & Johnson Surgical Vision, Inc. | Class II | N/A |