Volcano Corp: Volcano Visions Digital IVUS Catheter: PV.014P (Platinum), REF:85910P; PV.014P RX, REF: 014R; and PV.018, REF: 86700, 86700J used with Instructions for use.

Recall number

Z-2221-2025

Recalling firm

Volcano Corp

Product

Volcano Visions Digital IVUS Catheter: PV.014P (Platinum), REF:85910P; PV.014P RX, REF: 014R; and PV.018, REF: 86700, 86700J used with Instructions for use.

Status

Open, Classified

Initiated

2025-06-13

Posted

2025-07-30

Terminated

not on file

Reason

Reports of IVUS catheter and guide wire entanglement during radial-to-peripheral procedures, due to catheter use without appropriate sheath and/or guide catheter, which may require further intervention, such as surgical removal; Firm is restating instructions for use and adding: "Use a guide sheath of appropriate length to provide adequate support to the rapid exchange IVUS catheter and guidewire"

Root cause

not on file

Action

On 6/13/2025, correction notices were mailed to customers who were asked to do the following: As per standard practice, take precautions when advancing or removing a catheter in complex vessel anatomies. Do not force a catheter into a narrow vessel or tight stenosis. Be aware that vessel calcification, tortuosity, and untreated vessel spasm are key components of complex vascular anatomy. If the initial guidewire faces resistance or requires further manipulation, consider this to be an indicator of complex patient anatomy. The Instructions for Use currently contains the following related precautions for the user: "Do not advance the guide wire against significant resistance. If binding occurs between the catheter and the guide wire while inside the patient, CAREFULLY REMOVE BOTH the wire and catheter and do not use. If binding occurs outside of the patient, remove the catheter and do not use." Using a long radial sheath avoids this issue by preventing the catheter and guidewire from getting entangled within the sheath. The Instructions for Use highlights the minimum sheath/guide catheter Inner Diameter which does not prevent such complications; therefore, a new precaution will be added to the Instructions for Use: "Use a guide sheath of appropriate length to provide adequate support to the rapid exchange IVUS catheter and guidewire." If you need any further information or support concerning this issue, please contact your local Philips representative or Philips IGTD Customer Service: Phone: 1-800-722-9377, Option 1 Email: IGTD.CustomerInquiry@philips.com Hours of Operation: Monday - Friday 8:00AM - 5:00PM PST

Quantity

233,817

Distribution

Worldwide distribution - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY and the countries of BR, PL, SK, IT, DK, DE, GB, AT, KW, CR, ES, NL, LV, MT, IE, CH, ZA, RO, FI, PR, FR, CA, PA, IL, SE, PT, HR, GR, NZ, HK, TW, MY, TH, MX, AR, PE, AE, BG, AU, JP, ID, RS, CO, SG, BE.

Lot, serial or model codes

UDI-DI: 00845225002848, 00184360000037. Instructions for use: 300004875732_A Revision Date: 03/2021, 300004410212.A Release Date: 03/2021

510(k) numbers

["K150442","K152829"]

PMA numbers

not on file

Product code

OBJ

Firm FEI

3008363989

Firm city

San Diego

Firm state

CA

Firm country

not on file

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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