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Medtronic Xomed, Inc.

Medtronic Xomed, Inc. Recalls

All product recalls associated with Medtronic Xomed, Inc..

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Recall Summary

Total Recalls

606

Past Year

Class I (Serious)

Most Recent

Nov 2025

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.

Showing 601–606 of 606 recalls

Medtronic Xomed, Inc.: The product is a sheath meant to fit over a Nasopharyngos...

The sheaths in question have shafts that are one inch longer than required for the endoscope specified on the label.

FDAJan 29, 2004FL, ID, IN +12 more• Medtronic Xomed, Inc.

Medtronic Xomed, Inc.: Product is a device used in adenoid surgery and is labele...

The box label indicates that the product is a size 2 whereas a size 4 was packed inside.

FDAJan 29, 2004FL, ID, IN +12 more• Medtronic Xomed, Inc.

Medtronic, Inc.: Medtronic SiteSeer 5 F Tight Radius 145 Pigtail Cardiov...

Catheter distal tip may separate

FDAJan 14, 2004NC, WA• Medtronic, Inc.

1...29 3031

Page 31 of 31Next

Medtronic Surgical Navigation Tech, Inc: Fix pins associated with Stealth Station Treatment Guidan...

Surgical devices intended for single use were not labeled for single use.

FDAOct 31, 2003CA, FL, GA +3 more• Medtronic Surgical Navigation Tech, Inc

Medtronic, Inc.: Z2 Guiding Catheter 6 F JL3.5 SH Item No. : Z26JL35SH

The PTCA catheter is mislabeled: the curve style (Judkin Left vs. Judkin Right ) of the catheter may not correctly match the box label.

FDAMar 17, 2003AL, AR, KY +6 more• Medtronic, Inc.

Medtronic, Inc.: Z2 Guiding Catheter 6 F JR3.5 SH Item No. : Z26JR35SH

The PTCA catheter is mislabeled: the curve style (Judkin Left vs. Judkin Right ) of the catheter may not correctly match the box label.

FDAMar 17, 2003AL, AR, KY +6 more• Medtronic, Inc.