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