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All product recalls associated with Medtronic Xomed, Inc..
Total Recalls
1000
Past Year
896
Class I (Serious)
125
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
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'.
This recall involves plastic sippy/tumbler cups bearing the "Next Step" logo. The 7-ounce cup has an aqua blue cap and a yellow, rubber-like material covering the handles and bottom of the cup.
The recall involves the Weil-McLain Model 80, 88, 94, and LGB Packaged Commercial Boilers built from December 1, 2005 through October 26, 2006. The model information is written on a name plate or rating label on the front blue sheet metal jacket panels.