FDA Enforcement Class II Terminated

(1) Arterial Catheterization Kit, Part Number (PN): ASK-04018-CC; (2) Arterial Line Kit with Sharps Safety Features, PN: ASK-04510-HUM; (3) Arterial Line Kit with Sharps Safety Features, PN: ASK-04550-UHC; (4) Arterial Catheterization Kit, PN: NA-04550-X1A

Recall: Z-1330-2018 · Reported April 18, 2018

Enforcement

Recall Number
Z-1330-2018
Event ID
79512
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Arrow International Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
April 18, 2018
Initiation Date
December 22, 2017
Classification Date
April 10, 2018
Termination Date
May 27, 2020
Address
2400 Bernville Rd, Reading, PA, 19605-9607, United States

Description

(1) Arterial Catheterization Kit, Part Number (PN): ASK-04018-CC; (2) Arterial Line Kit with Sharps Safety Features, PN: ASK-04510-HUM; (3) Arterial Line Kit with Sharps Safety Features, PN: ASK-04550-UHC; (4) Arterial Catheterization Kit, PN: NA-04550-X1A

Reason

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

Code Info

Lot Numbers: (1) 13F17D0198, 13F17F0215; (2) 13F17E0029, 13F17E0537; (3) 13F17B0226, 13F17D0017, 13F17D0280; (4) 13F17A0122, 13F17C0342, 13F17E0364, 13F17E0827

Distribution

Distributed in all 50 U.S. states and the District of Columbia. Distributed in Bahamas, Canada, Mexico, Panama, and Singapore.