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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

1000

Past Year

579

Class I (Serious)

Most Recent

Dec 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 2921–2940 of 10937 recalls

Medtronic Sterile Blades (Medtronic) – Tip Break Risk (2021)

There was an increase in complaints related to tip breaks and wobble/vibration.

Moderate

FDAAug 31, 2021Nationwide• Medtronic Xomed, Inc.

DLP Left Heart Vent Catheters (Medtronic) – Wire Protrusion Risk (2021)

Potential for a wire protrusion through the left heart vent catheter tip

Moderate

FDAAug 24, 2021Nationwide• Medtronic Perfusion Systems

Action De Gala FuSion Gel (Aesthetics) – Bacterial Contamination (2021)

Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021, FDA published a Letter to Health Care Providers to further address this issue: https://www.fda.gov/medical-devices/letters-health-care-providers/stop-using-all-eco-med-ultrasound-gels-and-lotions-due-risk-bacterial-contamination-letter-health.

High

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Page 147 of 547Next

FDA

Aug 23, 2021

Nationwide

• Aesthetics Systems Usa Inc

Wild Keta Salmon Lox (Loki Fish) – Listeria Contamination (2021)

Listeria

Potential to be contaminated with Listeria monocytogenes.

Class IHigh

FDAAug 23, 2021IN, OR, WA• Loki Fish Company - Office

Donepezil HCL Tablets (Jubilant Cadista) – Subpotent Medication (2021)

Subpotent

Class IIILow

FDAAug 20, 2021Nationwide• Jubilant Cadista Pharmaceuticals, Inc.

Trulicity (Eli Lilly) – Labeling Strength Error (2021)

Labeling: Label error on declared strength - autoinjector devices labeled as 0.75 mg / 0.5 mL actually contain 1.5 mg / 0.5 mL of product.

Class IIModerate

FDAAug 19, 2021Nationwide• Eli Lilly & Company

AtomLab 500Plus Dose Calibrator (Biodex) – software deletion error (2021)

When deleting a previously entered custom isotope, the software deletes the isotope, but not the associated dial setting. Possible other stored custom isotopes may then have incorrect dial settings and may lead to an incorrect dose measurement and/or misadministration

High

FDAAug 16, 2021Nationwide• Biodex Medical Systems, Inc.