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FDA Medical Device Recalls (openFDA)

Innovatech Medical Resources L.P.: 3.5mm 90 Degree Part Number A1335-01 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-0621-2012
Recalling firm
Innovatech Medical Resources L.P.
Product
3.5mm 90 Degree Part Number A1335-01 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
Lot Number (QTY): 0933831-2 (3 units), 093534102 (1 unit), and 5L14150-A (1 unit)
Distribution
Nationwide Distribution including Texas
Lot, serial or model codes
Lot Numbers 0933831-2, 093534102, and 5L14150-A
510(k) numbers
["K082980"]
PMA numbers
not on file
Product code
GEI
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
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

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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

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