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Medtronic Neuromodulation

Medtronic Neuromodulation Recalls

All product recalls associated with Medtronic Neuromodulation.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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.

Showing 2841–2860 of 37665 recalls

Medtronic Recharger Kits (Medtronic) – Charging Session Issue (2024)

The Wireless Rechargers in the kits may be unable to enter a recharging session upon first use.

Moderate

FDASep 18, 2024Nationwide• Medtronic Neuromodulation

Quantimetrix Urine Control Set (McKesson) – Packaging Temperature Risk (2024)

The Quantimetrix Dipper Urinalysis Dipstick control was shipped without the validated summer packaging and may have been exposed to temperatures above 25C. This may lead to delay in patients' results.

Low

FDASep 17, 2024Nationwide• Mckesson Medical-Surgical Inc. Corporate Office 9954 Maryland Drive Deep Run Iii Ste. 4000 Richmond VA 23233

MST Duet Reusable Handle (MicroSurgical) – Pin Detachment Concern (2024)

Due to pin coming off of handles.

Moderate

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FDA

Sep 17, 2024

Nationwide

• MicroSurgical Technology Inc

IMAGEnet 6 Ophthalmic System (Topcon) – Probability Map Error (2024)

The overlay of visual field test locations on a probability map, as presented in IMAGEnet 6 in the so-called "Hood Report", is not appropriate as it can imply a structure/function correlation for which clinical evidence is not provided

Moderate

FDASep 17, 2024Nationwide• Topcon Medical Systems, Inc.

Cartesion Prime PET-CT (Canon) – Reconstruction Software Problem (2024)

Laceration Risk

When PET-CT system is executing reconstruction, if PET acquisition for another patient is performed (or PET reconstruction for another patient is performed from raw data processing), PET reconstruction control processing may hang up and PET reconstruction may stop as a result, which may necessitate repeat PET/CT examinations.

Moderate

FDASep 17, 2024AL, AZ, AR +15 more• Canon Medical System, USA, INC.

MEGA Intra-Aortic Balloon (Datascope) – Packaging Labeling Discrepancy (2024)

There is discrepant labeling on the inner and outer packaging of the device.

Low

FDASep 17, 2024Nationwide• Datascope Corp.

Check-Flo Performer Introducer Set (Cook) – Shaft Connection Problem (2024)

Cook Medical is conducting removal of a lot of Check-Flo Performer Introducer Set due to complaints that the white caps that connect the shaft to the hub of these products may disconnect.

Moderate

FDASep 16, 2024Nationwide• Cook Incorporated