Implantable Vascular Access system -- Infusion Ports with Silicone Rubber Catheter. Latex-Free Low Profile B Port, 6 Fr. Introducer Kit. Ref Product No. AP-06046
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-0276-2007
- Quantity
- 42
- 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-06046. Lot Number: MF2102346, MF2112623, MF2122946, MF3023531, MF3043934, MF3074943, MF3085287, MF3095692, MF4020550, MF4031019, MF4031353, MF4041638, MF4063174, MF4105485, MF5017413, MF5017546, MF5038769.
Root Cause
Other
Action Taken
The recall notification was sent out to their US customers on 9/29/2006.
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