Volcano Corp: Medical Device Recall in 2022 - (Recall #: Z-1270-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Philips OmniWire Pressure guide wire REF 89185J PN 300000252891

Product Classification:

Class II

Date Initiated: May 16, 2022

Date Posted: June 22, 2022

Recall Number: Z-1270-2022

Event ID: 90292

Reason for Recall:

Due to a potential failed sterilization process.

Status: Terminated

Product Quantity: 11 devices

Code Information:

Model Number: 89185J Part Number: 300000252891 UDI Code: (01)00845225003050(11)220309(17)250309(10)0302535768 Serial Numbers: 37583 37586 37590 37598 37612 37648 37655 37692 37694 37709 37719

Distribution Pattern:

U.S.: WA and WI O.U.S.: Canada

Voluntary or Mandated:

Voluntary: Firm initiated