Johnson & Johnson Recalls HEALON Viscoelastic Products Due to Surgical Instructions
Johnson & Johnson is recalling HEALON EndoCoat PRO and HEALON DUET PRO II viscoelastic products because surgical instructions may not adequately warn against forcing the cannula, which could cause eye injury.
- Product
- HEALON EndoCoat PRO, REF: 10300012 (US/CAN) HEALON DUET PRO II, REF: 10300016 (US/CAN) HEALON EndoCoat PRO, REF: 10301012 (EU); HEALON DUET PRO II, REF: 10301016 (EU)
- Category
- Medical Device
- Distribution
- Distributed nationwide