FDA Medical Device Recalls (openFDA)
Arrow International Inc: Implantable Vascular Access System -- Infusion Ports with Silicone Rubber Catheter. Latex-Free A Port. 9 Fr. Introducer Kit Ref Product No. AP-06013.
- Recall number
- Z-0286-2007
- Recalling firm
- Arrow International Inc
- Product
- Implantable Vascular Access System -- Infusion Ports with Silicone Rubber Catheter. Latex-Free A Port. 9 Fr. Introducer Kit Ref Product No. AP-06013.
- 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
- 331
- Distribution
- Nationwide. The firm is NOT recalling from international accounts.
- Lot, serial or model codes
- Product No. AP-06013. Lot Numbers: MF2102345, MF2112624, MF2122835, MF3013200, MF3023408, MF3023552, MF3033766, MF3054406, MF3074987, MF3075143, MF3095708, MF3105784, MF3116130, MF3116231, MF4016530, MF4020444, MF4020470, MF4041797, MF4062926, MF4073773, MF4084282, MF4094881, MF4116112, MF4126522, MF4126770, MF4126879, MF5017542, MF5028152, MF5038758, MF5049103, MF5059726, MF5060460, MF5081715, MF5082408, MF5092546, MF5103679, MF5113983, MF6014772, MF6026163, MF6036927.
- 510(k) numbers
- ["K875214","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