Recall Z-1334-2018— Arrow International Inc

Name: FDA recall Z-1334-2018
Creator: U.S. Food and Drug Administration
Published: 2017-12-22

Class II · Terminated

Class II FDA medical device recall by Arrow International Inc, initiated 2017-12-22, terminated 2020-05-27. It names one FDA 510(k) clearance: K940079. Product: Arrowg+ard Blue(R) PSI Kit, (1) For use with 7 - 7.5 Fr. Catheters Part Number (PN): ASK-29804-UHN2; (2) For use with 7.5 - 8 Fr. Catheters PN: ASK-29903-UCD. Reason: Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed..

Recalling firm: Arrow International Inc
Classification: Class II
Status: Terminated
Initiated: 2017-12-22
Terminated: 2020-05-27
Firm location: Reading, PA, United States

510(k) clearances named in this recall

1 on FDA's record

K940079 — ARROW PERCUTANEOUS SHEATH INTRODUCER KIT AK-07903Arrow Intl., Inc.·cleared 1994-11-30

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

Arrowg+ard Blue(R) PSI Kit, (1) For use with 7 - 7.5 Fr. Catheters Part Number (PN): ASK-29804-UHN2; (2) For use with 7.5 - 8 Fr. Catheters PN: ASK-29903-UCD

Reason for recall

Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.

Data sourced from openFDA. This site is unofficial and independent of the FDA.