Bard Peripheral Vascular Inc: Medical Device Recall in 2018 - (Recall #: Z-1762-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

POWERPORT ClearVUE Slim with Smooth Septum, 6F ChronoFlex Silk, Polyurethane Catheter, REF 1676300

Product Classification:

Class II

Date Initiated: February 8, 2018

Date Posted: May 16, 2018

Recall Number: Z-1762-2018

Event ID: 79841

Reason for Recall:

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

Status: Completed

Product Quantity: 1551 units

Code Information:

Lot Number Unique Device Identifier (UDI) REAN0062 (01)00801741110764(17)170628(10)REAN0062 REAP0628 (01)00801741110764(17)170828(10)REAP0628 REAU0228 (01)00801741110764(17)171228(10)REAU0228 REAW1710 (01)00801741110764(17)180331(10)REAW1710 REAY0677 (01)00801741110764(17)180531(10)REAY0677 REAY2493 (01)00801741110764(17)180331(10)REAY2493 REBQ0468 (01)00801741110764(17)180331(10)REBQ0468 REBS1274 (01)00801741110764(17)180930(10)REBS1274 REBS1900 (01)00801741110764(17)180930(10)REBS1900 REBT2147 (01)00801741110764(17)181130(10)REBT2147 REBV1310 (01)00801741110764(17)181231(10)REBV1310 REBW0863 (01)00801741110764(17)181231(10)REBW0863 REBX2269 (01)00801741110764(17)190430(10)REBX2269

Distribution Pattern:

Nationwide

Voluntary or Mandated:

Voluntary: Firm initiated