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FDA (Device enforcement)Recalled 2018-02-08class ii

Bard Peripheral Vascular Inc: POWERPORT ClearVUE Slim Implantable Port with Smooth Septum and Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter Custom Kit, REF CP00005

Is my product affected?

POWERPORT ClearVUE Slim Implantable Port with Smooth Septum and Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter Custom Kit, REF CP00005

  • UPC 00801741110894

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

What happened

Bard Peripheral Vascular Inc. has recalled 10 units of the POWERPORT ClearVUE Slim Implantable Port with Smooth Septum and Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter Custom Kit due to incorrect port flushing instructions on the Patient ID Card included with the device. The affected units were distributed nationwide and are identified by lot numbers REAN0056, REAN0203, REAP0773, and REBN0925.

The source document does not specify a remedy or corrective action for consumers who may have received this product.

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

Hazard

The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port with Smooth Septum contains incorrect port flushing instructions.

Details from the source

Reason for recall: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port with Smooth Septum contains incorrect port flushing instructions. Distribution: Nationwide Quantity: 10 units Lot/code info: Lot Number Unique Device Identifier (UDI) REAN0056 (01)00801741110894(17)170628(10)REAN0056 REAN0203 (01)00801741110894(17)170628(10)REAN0203 REAP0773 (01)00801741110894(17)170728(10)REAP0773 REBN0925 (01)00801741110894(17)180131(10)REBN0925

Source

Official record: FDA (Device enforcement) ↗

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

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