FDA Medical Device Recalls (openFDA)
ARROW INTERNATIONAL Inc.: Arrow Pressure Injectable Arrowg+ard Blue Plus Four-Lumen CVC, REF CDC-45854-P1A; catheter, intravascular, therapeutic, long-term greater than 30 days
- Recall number
- Z-0003-2024
- Recalling firm
- ARROW INTERNATIONAL Inc.
- Product
- Arrow Pressure Injectable Arrowg+ard Blue Plus Four-Lumen CVC, REF CDC-45854-P1A; catheter, intravascular, therapeutic, long-term greater than 30 days
- Status
- Open, Classified
- Initiated
- 2023-08-10
- Posted
- 2023-10-05
- Terminated
- not on file
- Reason
- This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
- Root cause
- Under Investigation by firm
- Action
- Teleflex/Arrow International issue an URGENT MEDICAL DEVICE RECALL notice on 08/10/2023 by FedEx 2nd day mail. The letter explained the problem, risk to patient, and requested the following actions: Medical facilities: Immediately cease use and distribution of affected product and quarantine for return. Distributors: Immediately cease use and distribution of affected product and quarantine for return. Provide a copy of this recall notice to all customers who have received impacted product. Request they complete the Acknowledgement Form and return it to you. Firm is requesting return of the affected product.
- Quantity
- 380 units
- Distribution
- US
- Lot, serial or model codes
- Batch/Lot number 13F22L0806
- 510(k) numbers
- ["K071538"]
- PMA numbers
- not on file
- Product code
- FOZ
- Firm FEI
- 3013162291
- Firm city
- Morrisville
- Firm state
- NC
- 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