FDA Enforcement
Class II
Completed
IceRod" 1.5 90¿ Cryoablation Needle
Recall: Z-0668-2021
·
Reported December 30, 2020
Enforcement
- Recall Number
- Z-0668-2021
- Event ID
- 86777
- Classification
- Class II
- Status
- Completed
- Product Type
- Devices
- Firm
- Boston Scientific Corporation
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- December 30, 2020
- Initiation Date
- November 18, 2020
- Classification Date
- December 22, 2020
- Address
- 1 Scimed Pl, N/A, Maple Grove, MN, 55311-1565, United States
Description
IceRod" 1.5 90¿ Cryoablation Needle
Reason
Complaint trend regarding needle shaft gas leaks.
Code Info
UPN: FPRPR3204 UDIs: 7290104830242, 7290104830242, 7290104830242, 7290104830242, 7290104830242, 7290104830242, 7290104830242 Batch Numbers: U0495, U0498, U0496, U0497, U0420, A0902, A0903
Distribution
Nationwide
Quantity
93 units