Z-1249-2020 Class II Terminated
FDA device recall Z-1249-2020 was initiated by Arrow International Inc on December 20, 2019 and is designated Class II. Reason for recall: Product lidstock contains the incorrect expiration date for the product The recall status is terminated (terminated February 25, 2021). Affected quantity: 1360.
Recall Details
- Product Type
- Devices
- Report Date
- February 26, 2020
- Initiation Date
- December 20, 2019
- Termination Date
- February 25, 2021
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1360
Product Description
Arrow EPIDURAL CATHETERIZATION KIT CK-02220
Reason for Recall
Product lidstock contains the incorrect expiration date for the product
Distribution Pattern
Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA
Code Information
Lot Number: 13F18A0713 13F18B0394