Arrow¿ EPIDURAL CATHETERIZATION KIT AK-05000
FDA Recall #Z-1245-2020 — Class II — December 20, 2019
Product Description
Arrow¿ EPIDURAL CATHETERIZATION KIT AK-05000
Reason for Recall
Product lidstock contains the incorrect expiration date for the product
Recalling Firm
Arrow International Inc — Reading, PA
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Devices
Product Quantity
870
Distribution
Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
Code Information
Lot Number: 13F18A0451
Status
Terminated
Voluntary / Mandated
Voluntary: Firm initiated