FDA Medical Device Recalls (openFDA)
Arrow International Inc: Cannon catheter hemodialysis catheterization set, 15 Fr x 36 cm
- Recall number
- Z-0084-04
- Recalling firm
- Arrow International Inc
- Product
- Cannon catheter hemodialysis catheterization set, 15 Fr x 36 cm
- Status
- Terminated
- Initiated
- 2003-09-16
- Posted
- 2003-11-01
- Terminated
- 2004-04-05
- Reason
- wrong product in box
- Root cause
- Other
- Action
- The recalling firm issued a recall letter to their direct customers dated 9/16/03. The recall letter explained the reason for recall and to return the product.
- Quantity
- 34 units
- Distribution
- The products were shipped to distributors in AL, AZ, CA, CO, FL, HI, IL, IN, KS, MD, MI, MN, MO, NC, NM, NY, OH, PA, TN, TX, VA, and WI. The products were shipped to government accounts in AZ, AK, DC, IN, SC, and VA. The products were shipped to hospitals nationwide.
- Lot, serial or model codes
- Catalog number CC-03600, Lot number RF3066991
- 510(k) numbers
- ["K010399"]
- PMA numbers
- not on file
- Product code
- KZH
- 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