FDA Medical Device Recalls (openFDA)
Innovatech Medical Resources L.P.: SideWinder Hip Wand Product Number AC2340-01 is an ablation wand Intended for resection, ablation, and coagulation of soft tissue, and hemostasis of blood vessels in arthroscopic and orthopedic procedures
- Recall number
- Z-0616-2012
- Recalling firm
- Innovatech Medical Resources L.P.
- Product
- SideWinder Hip Wand Product Number AC2340-01 is an ablation wand Intended for resection, ablation, and coagulation of soft tissue, and hemostasis of blood vessels in arthroscopic and orthopedic procedures
- Status
- Terminated
- Initiated
- 2011-08-08
- Posted
- 2012-01-11
- Terminated
- 2012-09-27
- Reason
- Product is being removed from the field due to an over-label issue.
- Root cause
- Reprocessing Controls
- Action
- Innovatech Medical Resources L.P. decided to recall all products resterilized and overlabeled at their facility. A firm representative would visit each customer and request that they remove the overlabeled product from their shelves and secure it. Customers could call the MSI office to get a RMA (Return Materials Authorization) for a refund on this product. For questions regarding this recall call 817-714-9066.
- Quantity
- 4 Units
- Distribution
- Nationwide Distribution including Texas
- Lot, serial or model codes
- Lot Number M305780-A
- 510(k) numbers
- K082980
- PMA numbers
- not on file
- Product code
- not on file
- Firm FEI
- 3009124511
- Firm city
- Midlothian
- Firm state
- TX
- 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
- 3e6df46828c1
- Size
- 288213574 bytes
- Published
- 2026-10-06
- Read
- 2026-10-07T03:20:25.099Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-14
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 3e6df46828c1, published 2026-10-06