FDA Medical Device Recalls (openFDA)
Angiodynamics, INC: AngioDynamics RITA Main Cable, 9 Pin to 14 Pin, REF 700-101892. RITA Main Cables are indicated for use with the RITA RF Generators and RITA electrosurgical devices.
- Recall number
- Z-1675-2013
- Recalling firm
- Angiodynamics, INC
- Product
- AngioDynamics RITA Main Cable, 9 Pin to 14 Pin, REF 700-101892. RITA Main Cables are indicated for use with the RITA RF Generators and RITA electrosurgical devices.
- Status
- Terminated
- Initiated
- 2013-06-11
- Posted
- 2013-07-10
- Terminated
- 2015-06-12
- Reason
- The RITA Main Cable product contains the incorrect Instructions for Use.
- Root cause
- Packaging process control
- Action
- Consignees were notified via certified mail on 06/11/2013 with an "Urgent Medical Device Field Safety Correction" notification. This included the correct Instructions for Use and the recommended actions.
- Quantity
- 13 units
- Distribution
- Worldwide Distribution, including the US, Austria, China, Italy, Russia and the UK.
- Lot, serial or model codes
- Catalog #700-101892, Lot number: 30.12
- 510(k) numbers
- ["K040989"]
- PMA numbers
- not on file
- Product code
- GEI
- Firm FEI
- 3017892510
- Firm city
- Manchester
- Firm state
- GA
- 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