Boston Scientific Corporation: IceRod" i-Thaw" Prostate Cryoablation Kit

Is my product affected?

IceRod" i-Thaw" Prostate Cryoablation Kit

• UPC 7290104830983

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

What happened

Boston Scientific Corporation is recalling the IceRod i-Thaw Prostate Cryoablation Kit due to a complaint trend regarding needle shaft gas leaks. The recall affects 947 units with UPN FPRPR3572 that were distributed nationwide.

The source does not specify a remedy or what affected consumers should do in response to 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: 947 units Lot/code info: UPN: FPRPR3572 UDIs: 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 7290104830983, 729010483

Source

Official record: FDA (Device enforcement) ↗

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

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