Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Terminated

Arrow JACC with Chlorag+ard Technology Jugular Axillosubclavian Central Catheter Product Code: CDC 43063 JX1A

FDA Recall Z-1804-2019 · Posted None

Recalling FirmArrow International Inc
Recall StatusTerminated
Product CodeLJS
Date Initiated2019-04-23
Date Terminated2021-01-13
Product Quantity12 units

Reason for Recall

Lidstock states the incorrect expiration date for the product

Firm Action

Arrow International initiated recall by letter dated April 23,2019 described the problem, health risk and action to take: If you have affected stock in inventory, immediately discontinue use and quarantine the products. 2. Complete the enclosed Acknowledgement Form indicating whether you do or do not have stock and fax it to 1-855-419-8507 or email to [email protected]. A customer service representative will contact you with a Return Goods Authorization (RGA) number and provide instructions for the return of products. Distributors requested to subrecall. Questions, contact your local sales representative or Customer Service at 1-866-396-2111.

Root Cause

Process control

Distribution Pattern

Nationwide Foreign:

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

↑