Boston Scientific Corporation: IcePearl" 2.1 CX Prostate Cryoablation Kit

Is my product affected?

IcePearl" 2.1 CX Prostate Cryoablation Kit

• UPC 7290104831041

Check against the official notice below — it lists the full affected range.

What happened

Boston Scientific Corporation is recalling 215 units of the IcePearl 2.1 CX Prostate Cryoablation Kit nationwide due to a complaint trend involving gas leaks in the needle shaft. The recalled units have UPN FPRPR3606 and UDI 7290104831041, and were distributed across multiple batch numbers ranging from A1171 to U1473.

The source document does not specify a remedy or instructions for what affected consumers should do regarding this recall.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

Complaint trend regarding needle shaft gas leaks.

Details from the source

Reason for recall: Complaint trend regarding needle shaft gas leaks. Distribution: Nationwide Quantity: 215 units Lot/code info: UPN: FPRPR3606 UDIs: 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041, 7290104831041 Batch Numbers: U1473, U1299, U1300, U1261, U1213, U1109, U1039, U1031, U0925, U0924, U0858, U0784, U0614, U0613, U0582, U0554, U0226, U0227, U0093, U0027, U0082, T0592, T0437, T0268, T0237, T0236, T0224, T0141, T0136, T0054, A7148, A7088, A7026, A7013, A6925, A6856, A6743, A6702, A2121, A2118, A1936, A1582, A1561, A1460, A1248, A1171

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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