PlainRecalls
FDA Devices Moderate Class II Terminated

Walrus Arterial Embolectomy Catheter The arterial embolectomy catheter is intended for use in removing arterial emboli.

Reported: October 12, 2016 Initiated: July 7, 2016 #Z-2911-2016

Product Description

Walrus Arterial Embolectomy Catheter The arterial embolectomy catheter is intended for use in removing arterial emboli.

Reason for Recall

Arrow is recalling due to incorrect labeling of products.

Details

Recalling Firm
Arrow International Inc
Units Affected
2,425 catheters
Distribution
US Nationwide Distribution
Location
Reading, PA

Frequently Asked Questions

What product was recalled?
Walrus Arterial Embolectomy Catheter The arterial embolectomy catheter is intended for use in removing arterial emboli.. Recalled by Arrow International Inc. Units affected: 2,425 catheters.
Why was this product recalled?
Arrow is recalling due to incorrect labeling of products.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 12, 2016. Severity: Moderate. Recall number: Z-2911-2016.