Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Medtronic Neuromodulation

Medtronic Neuromodulation Recalls

All product recalls associated with Medtronic Neuromodulation.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

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 17961–17980 of 21320 recalls

Medtronic Neuromodulation: Medtronic DBS" 3387S-40 Lead Kit for Deep Brain Stimulati...

Medtronic has received reports of DBS" leads being damaged at the proximal connector end of the lead when the lead cap is used in the implant procedure. The lead damage is the result of excessive torsion and / or tensile lading of the proximal connector end of the lead. Data also suggest that excessive torque while tightening or loosening the setscrews may twist the setscrew connector block and d

FDAJun 14, 2008AL, AZ, AR +46 more• Medtronic Neuromodulation

Medtronic Neuromodulation: Medtronic DBS" 3389S-40 Lead Kit for Deep Brain Stimulati...

FDAJun 14, 2008AL, AZ, AR +46 more• Medtronic Neuromodulation

Medtronic Neuromodulation: Medtronic DBS" 3387 Lead Kit for Deep brain stimulation, ...

1...897 898899900 901...1066

Page 899 of 1066Next

FDAJun 14, 2008AL, AZ, AR +46 more• Medtronic Neuromodulation

Playsafe Spinning Quad Merry-Go-Rounds (Pacific Cycle) – fall risk (2008)

The Playsafe Spinning Quad Merry-Go-Round has four yellow plastic seats and black and silver metal bars.

CPSCJun 12, 2008Nationwide• Pacific Cycle Inc., of Madison, Wis.

Ventana Medical Systems Inc: Benchmark XT/LT and Discovery XT Model Numbers: N750-B...

Ventana Medical System is initiating the recall of the BenchMark and DISCOVERY series instruments because there is a possibility that the heating element could separate from the underside of the heater cap and cause a non-staining or inconsistent staining event. Additionally, the system may not detect this anomaly and therefore it may not generate an error message for the slide position.

Class IIModerate

FDAJun 12, 2008Nationwide• Ventana Medical Systems Inc

Infra-Red Sauna Rooms (Waterstar Electronic) – fire hazard (2008)

Fire/Burn Risk

The recalled infra-red sauna rooms are made of wood and include the following model numbers: IC I, IC II, IC III, IC IV, and IC V. The model number is indicated on the serial plate located on the back of the machine, in the lower right hand corner. IC I (1-Person) Dimensions: 35.5"x41.5"x75"(in) IC II (2-Person) Dimensions: 47"x47"x75"(in) IC III (3-Person) Dimensions: 60"x49"x75"(in) IC IV (4-Person) Dimensions: 69"x53"x75"(in) IC V (Corner) Dimensions: 59"x23.5"x49x75"(in)

CPSCJun 12, 2008Nationwide• Xuzhou Waterstar Electronic Co.

Ventana Medical Systems Inc: Benchmark XT/LT and Discovery XT Model Numbers: N750-BMK...

FDAJun 12, 2008Nationwide• Ventana Medical Systems Inc

ICU Medical, Inc.: Hospira Intralock Lipid Compatible 3-Way Stopcock, Item N...

Improper orientation of the stopcock handle questions whether there is an adequate gas path to assure sterility, which presents a possible compromise of sterility.

FDAJun 11, 2008Nationwide• ICU Medical, Inc.

Roche Diagnostics Corp.: Roche Diagnostics NAPA2, N-Acetyl-Procainamide, COBAS INT...

Some of the labels are glossy, resulting in the bar code being difficult to read by the bar code reader.

FDAJun 11, 2008Nationwide• Roche Diagnostics Corp.

ICU Medical, Inc.: Hospira Monitoring Kit (PA Line) with 03ml Flush Device f...

Improper orientation of the stopcock handle questions whether there is an adequate gas path to assure sterility, which presents a possible compromise of sterility.

FDAJun 11, 2008Nationwide• ICU Medical, Inc.

Roche Diagnostics Corp.: Roche Diagnostics CREP2, Creatinine Plus Ver. 2, COBAS IN...

Some of the labels are glossy, resulting in the bar code being difficult to read by the bar code reader.

FDAJun 11, 2008Nationwide• Roche Diagnostics Corp.

Roche Diagnostics Corp.: Roche Diagnostics HDLC3, HDL-Cholesterol Plus 3rd Generat...

Some of the labels are glossy, resulting in the bar code being difficult to read by the bar code reader.

FDAJun 11, 2008Nationwide• Roche Diagnostics Corp.

Roche Diagnostics Corp.: Roche Diagnostics IRON2, Iron Gen. 2, COBAS INTEGRA, coba...

Some of the labels are glossy, resulting in the bar code being difficult to read by the bar code reader.

FDAJun 11, 2008Nationwide• Roche Diagnostics Corp.

ICU Medical, Inc.: ICU Medical, Inc. Cath Lab Kit W/3Port "ON" Manifold, Was...

Improper orientation of the stopcock handle questions whether there is an adequate gas path to assure sterility, which presents a possible compromise of sterility.

FDAJun 11, 2008Nationwide• ICU Medical, Inc.

ICU Medical, Inc.: Hospira Left Heart Kit for Southwestern M.C. , Item Numbe...

Improper orientation of the stopcock handle questions whether there is an adequate gas path to assure sterility, which presents a possible compromise of sterility.

FDAJun 11, 2008Nationwide• ICU Medical, Inc.

Roche Diagnostics Corp.: Roche Diagnostics LDL_C, LDL- Cholesterol Plus 2nd genera...

Some of the labels are glossy, resulting in the bar code being difficult to read by the bar code reader.

FDAJun 11, 2008Nationwide• Roche Diagnostics Corp.

Varian Medical Systems Oncology Systems: Varian Medical Systems Eclipse device, model H48, Version...

Software anomaly in which swapping IDs of planning fields can produce inconsistencies between dose matrix and field parameters.

FDAJun 11, 2008Nationwide• Varian Medical Systems Oncology Systems

Roche Diagnostics Corp.: Roche Diagnostics ALBT2, Tina-quant Albumin Gen. 2, COBAS...

Some of the labels are glossy, resulting in the bar code being difficult to read by the bar code reader.

FDAJun 11, 2008Nationwide• Roche Diagnostics Corp.

Roche Diagnostics Corp.: Roche Diagnostics STFR Tina-quant Soluble Transferrin Rec...

Some of the labels are glossy, resulting in the bar code being difficult to read by the bar code reader.

FDAJun 11, 2008Nationwide• Roche Diagnostics Corp.

Siemens Medical Solutions USA, Inc.: Siemens brand Ultrasound Transducer 17L5HD used with ACUS...

The product assembly can cause a failure of the transducer which results in a double and/or overlapped image which may ultimately result in misleading or false information, inability to accurately diagnose, incorrect positioning/locating/insertion of the biopsy needle and/or an interruption during the biopsy procedure.

FDAJun 6, 2008Nationwide• Siemens Medical Solutions USA, Inc.