Medtronic Xomed, Inc. AccuGuide Injection Needles (Surface electrodes) The AccuGuide EMG Injection Needle, product 8263210, contains 5 individually packaged and sterilized injection needles and 10 nonsterile surface electrodes that are packaged 2 per non-breathable pouch, but are not sterilized. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
AccuGuide Injection Needles (Surface electrodes) The AccuGuide EMG Injection Needle, product 8263210, contains 5 individually packaged and sterilized injection needles and 10 nonsterile surface electrodes that are packaged 2 per non-breathable pouch, but are not sterilized.
Brand
Medtronic Xomed, Inc.
Lot Codes / Batch Numbers
Lot Numbers: 45648300, 46526000, 46709500, 48166300
Products Sold
Lot Numbers: 45648300, 46526000, 46709500, 48166300
Medtronic Xomed, Inc. is recalling AccuGuide Injection Needles (Surface electrodes) The AccuGuide EMG Injection Needle, product 8263 due to A labeling discrepancy was internally identified for the surface electrode component of REF 8263210 AccuGuide EMG Injection Needle, 30G X 25MM. The o. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
A labeling discrepancy was internally identified for the surface electrode component of REF 8263210 AccuGuide EMG Injection Needle, 30G X 25MM. The outside box label correctly indicates 'Content: 5 sterile Injection Needles and 10 non-sterile Surface electrodes'; however, the pouches for the 10 surface electrodes inside the box are incorrectly labeled as 'sterile'.
Recommended Action
Per FDA guidance
Each consignee contacted via telephone 01/22/2007, and then sent a follow-up fax letter 02/02/2007, which explained the issue, and the options for dispositioning any product that they still had in stock. Since firm has determined that the risk of keeping and using these devices is negligible to no risk, as they are intended to be and typically used in a non-sterile manner, the firm is offering the consignees the option to keep their devices or have them replaced.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026