Implantable Vascular Access System -- Infusion Ports with Silicone Rubber Catheter. Latex-Free A(2) Port, 10 Fr. Introducer Kit Ref Product No. AP-06530
This recall has been terminated (originally issued December 19, 2006).
- Company
- Arrow International Inc
- Recall Initiated
- September 29, 2006
- Posted
- December 19, 2006
- Terminated
- June 4, 2007
- Recall Number
- Z-0273-2007
- Quantity
- 210
- Firm Location
- Reading, PA
- Official Source
- View on FDA website ↗
Reason for Recall
Catheter has separated from the infusion port body.
Distribution
Nationwide. The firm is NOT recalling from international accounts.
Lot / Code Info
Product No: AP-06530. Lot Numbers: 11750, 11999, 12059, MF4031397, MF4042081, MF4062934, MF4063103, MF4073794, MF5027702, MF5059738, MF5060177, MF5060656, MF5081903, MF5103211, MF6036473, MF6036909, MF6068938, MS3100148.
Root Cause
Other
Action Taken
The recall notification was sent out to their US customers on 9/29/2006.
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