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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

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.

Showing 1841–1860 of 17592 recalls

Intellis Programmer (Medtronic) – Session Establishment Issue (2023)

Medtronic has discovered an instance in which the Intellis A710 Clinician Programmer Application (CP App) could no longer establish a session with the Implantable Neurostimulator (INS) which resulted in the inability for the clinician to adjust stimulation parameters. In the event of this issue, the patient may receive inadequate or excessive therapy and experience non-optimal pain relief.

High

FDADec 19, 2023Nationwide• Medtronic Neuromodulation

Acu-Loc Bone Plates (Acumed) – Distribution Clearance Issue (2023)

Distribution without Pre-Market Clearance

Moderate

FDADec 19, 2023Nationwide• Acumed LLC

iQ Waste Well Adapter (Beckman Coulter) – Cannula Rust Risk (2023)

Beckman Coulter has become aware that the cannula, which is found in the Flowcell and the iQClear Rinse Waste Well Assembly, may rust. Rust from the cannula has the potential to generate erroneous results.

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Moderate

FDADec 19, 2023Nationwide• Beckman Coulter, Inc.

DxU Microscopy Analyzers (Beckman Coulter) – Cannula Rust Risk (2023)

Moderate

FDADec 19, 2023Nationwide• Beckman Coulter, Inc.

Member's Mark Cheddar (Biery Cheese) - Foreign Material (2023)

Foreign Material - Glove remnants

Class IIModerate

FDADec 18, 2023IL, IN, MO +1 more• Biery Cheese Company

Spyder F3 (Can-Am) – Mirror Lens Dislodge Risk (2023)

Bombardier Recreational Products, Inc. (Bombardier) is recalling certain 2023 Can-Am F3 and F3-S motorcycles. The rearview mirror lens may dislodge from the housing.

Moderate

NHTSADec 17, 2023Nationwide• CAN-AM

ESG PK Cutting Forceps (Olympus) – Jaw Fracture Risk (2023)

The jaw may fracture prior to the procedure during the inspection instructed per the IFU, or during the procedure.

High

FDADec 15, 2023Nationwide• Olympus Corporation of the Americas

Can-Am Ryker (Can-Am) – Fuel Pump Impeller Swelling (2023)

Bombardier Recreational Products, Inc. (Bombardier) is recalling certain 2019-2023 Can-Am Ryker motorcycles. The impeller may swell, causing the high-pressure fuel pump to fail.

High

NHTSADec 15, 2023Nationwide• CAN-AM

Coachmen Concord (Coachmen) – Air Suspension Line Issue (2023)

Forest River, Inc. (Forest River) is recalling certain 2023-2024 Coachmen Concord CNC321DSF motorhomes. The air suspension air line may be incorrectly installed near the exhaust, which can cause a sudden loss of rear suspension.

High

NHTSADec 15, 2023Nationwide• COACHMEN

Ranger XP Kinetic ROVs (Polaris) – Crash Risk (2023)

This recall involves Model Year 2023-2024 RANGER XP Kinetic vehicles. The vehicles were sold in the following colors: camouflage and white. They were sold in three-seat configurations and have "POLARIS" stamped on the front grille. The model number and VIN are printed on a portion of the left rear frame (on the driver's side of the vehicle) under the cargo box.

High

CPSCDec 14, 2023Nationwide• Polaris Industries Inc., of Medina, Minnesota

Can-Am Side-By-Side Vehicles (BRP) – Injury Hazard (2023)

This recall involves Model Year 2022 and 2023 Can-Am Commander series, Defender series, Maverick Trail series equipped with an HD7 or 700 engines side-by-side vehicles with model number model year 2022 and 2023. The vehicles were sold in various colors. The brand and model name are on the vehicle's sides.

High

CPSCDec 14, 2023Nationwide• BRP Mexico, of Mexico

Spectral CT on Rails (Philips) – Image Labeling Error (2023)

A software issue that can incorrectly label all captured images that may lead to misdiagnosis and subsequent incorrect treatment.

High

FDADec 13, 2023Nationwide• PHILIPS MEDICAL SYSTEMS

Spectral CT 7500 (Philips) – Image Labeling Error (2023)

A software issue that can incorrectly label all captured images that may lead to misdiagnosis and subsequent incorrect treatment.

High

FDADec 13, 2023Nationwide• PHILIPS MEDICAL SYSTEMS

Azurion System (Philips) – Imaging Functionality Loss (2023)

System may exhibit a loss of imaging functionality and data due to an issue which can cause the system to continuously restart. If the issue occurs during a procedure, there may be a delay and/or abortion of the procedure.

Moderate

FDADec 12, 2023Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Paparrela-Type Vent Tube (Olympus) – Expiration Date Missing (2023)

The expiration date is missing from the primary (inner) packaging. The secondary (outer) box label correctly states the expiration date of February 12, 2033, for this lot

Moderate

FDADec 11, 2023Nationwide• Olympus Corporation of the Americas

Sertraline Tablets (Legacy) – Product Comingling Risk (2023)

CGMP Deviations: Inadequate line clearance which may result in a potential comingling of product.

Class IIModerate

FDADec 11, 2023AR, CA• Legacy Pharmaceutical Packaging LLC

Duodenovideoscope Distal Cover (Olympus) – Detachment Risk (2023)

Fire/Burn Risk

Single Use Distal Cover MAJ-2315 may unexpectedly detach from the duodenoscope during use result include the risk of mucosal injury, tissue damage, bleeding, perforation, or obstruction due to retained distal cover in the gastrointestinal tract that would require urgent medical intervention for removal, and/or burns from the use an uncovered duodenoscope distal end. Detachment of a distal cover in the oral cavity may result in aspiration, airway obstruction, or respiratory distress and would require immediate medical intervention for removal.

Very High

FDADec 8, 2023Nationwide• Olympus Corporation of the Americas

Azurion FlexArm System (Philips) – Connectivity Loss (2023)

Loss of connectivity between the FlexArm and the Table due to a software issue.

High

FDADec 8, 2023Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Pepper Gel Spray (Security Equipment) – Operational failure (2023)

Fire/Burn Risk

This recall involves SABRE Aim & Fire Pepper Gel with Training Canisters with model number SDP-G-03. The canisters look like a toy gun and have a black handle with an orange body. Only units with the expiration date of 9/2027 are included in the recall. The expiration date can be found on the white label on the side of the canisters.

Moderate

CPSCDec 7, 2023Nationwide• Security Equipment Corporation, of Fenton, Missouri

MINC+ Benchtop Incubator (Cook) – Temperature Control Issue (2023)

The MINC+ device is susceptible to losing temperature control of electrostatic discharge (static electricity) is applied to the lid of the device. This may lead to embryo degeneration necessitating an additional medical procedure for the patient.

Moderate

FDADec 7, 2023CA, IN, LA +2 more• Cook Medical Llc