PlainRecalls
FDA Devices Moderate Class II Terminated

Large Volume Abdominal Paracentesis Kit

Reported: April 11, 2018 Initiated: October 24, 2017 #Z-1297-2018

Product Description

Large Volume Abdominal Paracentesis Kit

Reason for Recall

Product packaging may not be completely sealed.

Details

Recalling Firm
Arrow International Inc
Units Affected
30,577 eaches
Distribution
Nationally
Location
Reading, PA

Frequently Asked Questions

What product was recalled?
Large Volume Abdominal Paracentesis Kit. Recalled by Arrow International Inc. Units affected: 30,577 eaches.
Why was this product recalled?
Product packaging may not be completely sealed.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 11, 2018. Severity: Moderate. Recall number: Z-1297-2018.