IceRod" 1.5 MRI 90¿ Cryoablation Needle¿
Check against the official notice below — it lists the full affected range.
Boston Scientific Corporation is recalling the IceRod 1.5 MRI 90° Cryoablation Needle due to a complaint trend regarding needle shaft gas leaks. The recall affects 3,894 units distributed nationwide with UPN FPRPR3195 and UDI 7290104830297.
The source does not specify a remedy or recommended consumer action.
Written by software from the official notice below. Not reviewed by a lawyer.
Complaint trend regarding needle shaft gas leaks.
Reason for recall: Complaint trend regarding needle shaft gas leaks. Distribution: Nationwide Quantity: 3,894 units Lot/code info: UPN: FPRPR3195 UDIs: 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 7290104830297, 729010483
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.