← Search recalls
FDA (Device enforcement)Recalled 2020-11-18class ii

Boston Scientific Corporation: IceSphere" 1.5 90¿ Cryoablation Needle

Is my product affected?

IceSphere" 1.5 90¿ Cryoablation Needle

  • UPC 7290104830945

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

What happened

Boston Scientific Corporation is recalling 2,429 units of the IceSphere 1.5 90° Cryoablation Needle due to a complaint trend regarding gas leaks in the needle shaft. The product was distributed nationwide and is identified by UPN FPRPR3560 and multiple batch numbers ranging from U1454 through A1786.

The recall record does not specify a remedy or instructions for what affected consumers should do.

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: 2,429 units Lot/code info: UPN: FPRPR3560 UDIs: 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945, 7290104830945 Batch Numbers: U1454, U1455, U1456, U1420, U1421, U1325, U1326, U1328, U1327, U0435, U0432, U0369, U0351, U0352, T0403, T0402, T0395, T0394, T0305, T0146, T0126, T0006, T0023, T0024, T0018, T0015, A7205, A6966, A6967, A6969, A6968, A6943, A6942, A6917, A6918, A2089, A2090, A1858, A1857, A1848, A1847, A1823, A1824, A1819, A1818, A1811, A1812, A1801, A1802, A1794, A1793, A1785, A1786,

Source

Official record: FDA (Device enforcement) ↗

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

Related recalls

All FDA (Device enforcement) recalls

Hurt by this product? Start a free Case Check

ProductRisk is not a law firm and does not provide legal services or legal advice. ProductRisk is a free consumer product-safety information service operated by Plaintify, Inc., a technology company. If you ask to be connected with a law firm, any legal services are provided by that firm — not by ProductRisk or Plaintify.

Privacy · Plaintify