Detachable Coil System Recall: J&j Medtech/cerenovus Inc. Remove Cerepak Detachable Coil System
Recall Summary Johnson & Johnson MedTech/CERENOVUS is recalling CEREPAK Detachable Coil Systems because the coils fail to detach from the delivery system more often than expected. This coil system is used in medical procedures to treat certain brain conditions. The recall affects patients who have received or may receive this device.
- Recalling firm
- Detachable Coil System Recall
- Product
- MedTech/CERENOVUS is removing CEREPAK Detachable Coil Systems due to a higher than expected failure to detach rate
- Reason
- MedTech/CERENOVUS is removing CEREPAK Detachable Coil Systems due to a higher than expected failure to detach rate
- Category
- drug recall
- Country
- United States
- Agency
- FDA-MEDWATCH-RSS
- Recall date
- 2026-02-05
- Status
- Ongoing
Official recall notice from FDA-MEDWATCH-RSS
Recall details on Nibble Recalls: https://trynibble.app/recalls/256a9c2b-71e0-4524-9fee-48c503d407fe