FDA Medical Device Recalls (openFDA)
Arrow International Inc: Implantable Vascular Access system -- Infusion Ports with Silicone Rubber Catheter. Latex-Free A Port, 10 Fr. Introducer Kit. Ref Product No. AP-06520
- Recall number
- Z-0275-2007
- Recalling firm
- Arrow International Inc
- Product
- Implantable Vascular Access system -- Infusion Ports with Silicone Rubber Catheter. Latex-Free A Port, 10 Fr. Introducer Kit. Ref Product No. AP-06520
- Status
- Terminated
- Initiated
- 2006-09-29
- Posted
- 2006-12-19
- Terminated
- 2007-06-04
- Reason
- Catheter has separated from the infusion port body.
- Root cause
- Other
- Action
- The recall notification was sent out to their US customers on 9/29/2006.
- Quantity
- 4940
- Distribution
- Nationwide. The firm is NOT recalling from international accounts.
- Lot, serial or model codes
- Product No. AP-06520. Lot Number: MF1033516, MF2071649, MF2081937, MF2082002, MF2092208, MF2092278, MF2102373, MF2102462, MF2112595, MF2112688, MF2122960, MF3013060, MF3013065, MF3013198, MF3013279, MF3013308, MF3023367, MF3023427, MF3033567, MF3033642, MF3033732, MF3043847, MF3043910, MF3044134, MF3054228, MF3054338, MF3054447, MF3054465, MF3064645, MF3064763, MF3064833, MF3074927, MF3075118, MF3085281, MF3095491, MF3095574, MF3095611, MF3105931, MF3106006, MF3116245, MF3126277, MF3126278, MF3126318, MF3126396, MF3126417, MF3126450, MF4016582, MF4016635, MF4020551, MF4020553, MF4020806, MF4031020, MF4031582, MF4041771, MF4041936, MF4052333, MF4063058, MF4073792, MF4083964, MF4084041, MF4084292, MF4094582, MF4094706, MF4105124, MF4105261, MF4105486, MF4105803, MF4116118, MF5017414, MF5017549, MF5027701, MF5028033, MF5028158, MF5038602, MF5050176, MF5059737, MF5060355, MF5060468, MF5071341, MF5081670, MF5081671, MF5081762, MF5081870, MF5081902, MF5082122, MF5082249, MF5092841, MF5093006, MF5103341, MF5103508, MF5113683, MF5113875, MF5114153, MF5124319, MF5124528, MF6014777, MF6025871, MF6026069, MF6026200, MF6036711, MF6057765, MF6058113, MF6058190, MF6058298, MF6068660, MF6079304, MF6089737, MF6089985, MS3110155, MS3110156, MS3110157, MS3110158, MS4031056, MS4031058, MS4031059, MS4031065.
- 510(k) numbers
- ["K882230","K921475"]
- PMA numbers
- not on file
- Product code
- LJT
- 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