RecallDepth

Implantable Vascular Access System -- Infusion Ports with Silicone Rubber Catheter. Latex-Free Low Profile Port. 6 Fr. Introducer Kit. Ref. Product No. AP-06016.

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-0283-2007
Quantity
21
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-06016. Lot Numbers: MF2092160, MF2092258, MF4031012, MF4041798, MF4063372, MF4073836, MF4105283, MF6015284, MF6026177.

Root Cause

Other

Action Taken

The recall notification was sent out to their US customers on 9/29/2006.

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