PlainRecalls
FDA Devices Moderate Class II Terminated

Arrow EPIDURAL CATHETERIZATION COMPONENT EC-05000

Reported: February 26, 2020 Initiated: December 20, 2019 #Z-1251-2020

Product Description

Arrow EPIDURAL CATHETERIZATION COMPONENT EC-05000

Reason for Recall

Product lidstock contains the incorrect expiration date for the product

Details

Recalling Firm
Arrow International Inc
Units Affected
540
Distribution
Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
Location
Reading, PA

Frequently Asked Questions

What product was recalled?
Arrow EPIDURAL CATHETERIZATION COMPONENT EC-05000. Recalled by Arrow International Inc. Units affected: 540.
Why was this product recalled?
Product lidstock contains the incorrect expiration date for the product
Which agency issued this recall?
This recall was issued by the FDA Devices on February 26, 2020. Severity: Moderate. Recall number: Z-1251-2020.