FDA Enforcement
Class II
Completed
IceRod" 1.5 MRI Cryoablation Needle¿
Recall: Z-0679-2021
·
Reported December 30, 2020
Enforcement
- Recall Number
- Z-0679-2021
- 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 MRI Cryoablation Needle¿
Reason
Complaint trend regarding needle shaft gas leaks.
Code Info
UPN: FPRPR3193 UDIs: 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273, 7290104830273 Batch Numbers: U1440, U1441, U1311, U1312, U1015, U1016, U0462, U0461, U0050, U0030, T0520, T0521, T0157, T0158, A7135, A7134, A6987, A6986, A6707, A6708, A6689, A6688, A1730, A1731, A1149, A1150
Distribution
Nationwide
Quantity
772 units