Arrow International Inc Cannon II Plus, Hemodialysis Catherization Set, Long-Term Access. Catheter Length, Cuff to Tip: 19cm, CSD-15242-SP, Intended for single use only, Sterile, Rx only, Arrow International, Inc., 2400 Bernville Road, Reading, PA 19605, USA The product is used for long term hemodialysis vascular access. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Cannon II Plus, Hemodialysis Catherization Set, Long-Term Access. Catheter Length, Cuff to Tip: 19cm, CSD-15242-SP, Intended for single use only, Sterile, Rx only, Arrow International, Inc., 2400 Bernville Road, Reading, PA 19605, USA The product is used for long term hemodialysis vascular access.
Brand
Arrow International Inc
Lot Codes / Batch Numbers
Lot# RL7065083, RL7064902, RL7054801, RL7024113, RL6103474, RL6093296, RL6083017, RL6082996, RL6062685, RL5101072, and RL5090957
Products Sold
Lot# RL7065083, RL7064902, RL7054801, RL7024113, RL6103474, RL6093296, RL6083017, RL6082996, RL6062685, RL5101072, and RL5090957
Arrow International Inc is recalling Cannon II Plus, Hemodialysis Catherization Set, Long-Term Access. Catheter Length, Cuff to Tip: 19cm due to The tips may not have been adequately welded to the catheter body.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The tips may not have been adequately welded to the catheter body.
Recommended Action
Per FDA guidance
Consignees were notified by letter on/about 06/10/2008. They were instructed to: 1. Cease use and distribution and quarantine all affected product immediately. 2. Contact Arrows Customer Service Department for a Return Authorization Number, enter the number on an enclosed Recall Acknowledgement & Stock Status Form and 3. Immediately fax back the form to Arrow International. All affected product is to be returned to Arrow International. A letter containing the recall information was enclosed for physicians who have implanted catheters. Contact Arrow's Customer Service at 1-800-523-8446 for assistance.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026