FDA Medical Device Recalls (openFDA)
Arrow International Inc: Arrow PICC powered by Arrow VPS Stylet Product Code: ASK45041JHVA
- Recall number
- Z-1787-2019
- Recalling firm
- Arrow International Inc
- Product
- Arrow PICC powered by Arrow VPS Stylet Product Code: ASK45041JHVA
- Status
- Terminated
- Initiated
- 2019-04-23
- Posted
- not on file
- Terminated
- 2021-01-13
- Reason
- Lidstock states the incorrect expiration date for the product
- Root cause
- Process control
- 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 recalls@teleflex.com. 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.
- Quantity
- 66 units
- Distribution
- Nationwide Foreign:
- Lot, serial or model codes
- Batch Code: 23F17C0310
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LJS
- Firm FEI
- 3015859709
- Firm city
- Reading
- Firm state
- PA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28