PlainRecalls
FDA Devices Moderate Class II Ongoing

Arrow ErgoPack Pressure Injectable One-Lumen PICC, REF CDC-05541-HPK1A; catheter, intravascular

Reported: September 27, 2023 Initiated: August 10, 2023 #Z-2590-2023

Product Description

Arrow ErgoPack Pressure Injectable One-Lumen PICC, REF CDC-05541-HPK1A; catheter, intravascular

Reason for Recall

This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.

Details

Recalling Firm
ARROW INTERNATIONAL Inc.
Units Affected
190 units
Distribution
US Nationwide distribution.
Location
Morrisville, NC

Frequently Asked Questions

What product was recalled?
Arrow ErgoPack Pressure Injectable One-Lumen PICC, REF CDC-05541-HPK1A; catheter, intravascular. Recalled by ARROW INTERNATIONAL Inc.. Units affected: 190 units.
Why was this product recalled?
This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 27, 2023. Severity: Moderate. Recall number: Z-2590-2023.