PlainRecalls
FDA Devices Moderate Class II Terminated

Radial Artery Catheterization Kit with Sharps Safety Features Permits access to the peripheral arterial circulation. The safety feature is intended to help minimize the risk of sharps injuries when using the device.

Reported: September 14, 2016 Initiated: August 8, 2016 #Z-2741-2016

Product Description

Radial Artery Catheterization Kit with Sharps Safety Features Permits access to the peripheral arterial circulation. The safety feature is intended to help minimize the risk of sharps injuries when using the device.

Reason for Recall

Shipping carton labeling error.

Details

Recalling Firm
Arrow International Inc
Units Affected
690 kits
Distribution
Nationwide Distribution to OH, IN, TN, NC, and KY.
Location
Reading, PA

Frequently Asked Questions

What product was recalled?
Radial Artery Catheterization Kit with Sharps Safety Features Permits access to the peripheral arterial circulation. The safety feature is intended to help minimize the risk of sharps injuries when using the device.. Recalled by Arrow International Inc. Units affected: 690 kits.
Why was this product recalled?
Shipping carton labeling error.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 14, 2016. Severity: Moderate. Recall number: Z-2741-2016.