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Medtronic Neurosurgery

Medtronic Neurosurgery Recalls

All product recalls associated with Medtronic Neurosurgery.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

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 36701–36720 of 37661 recalls

Medtronic Neurosurgery: Channel Neuroendoscope, Standard Resolution, 21.6 cm. ...

Size mix-up. 13 cm product may be labeled as 21.6 mm and visaversa.

FDASep 15, 2003CO, GA, TN• Medtronic Neurosurgery

ConMed Electrosurgery: Hyfrecator 20)0 Electrosurgical Unit. Hyfrecator 2000, P/...

The Hyfrecator 2000 units were released without documented adherence to their voltage output specification.

FDASep 15, 2003CA, CT, IL +1 more• ConMed Electrosurgery

Philips Medical Systems (Cleveland) Inc: Philips Odyssey LX Workstations, used with Axis, Irix, o...

Due to a software anomaly, an incorrect patient name may be transmitted with image to Odyssey workstation.

FDASep 15, 2003Nationwide• Philips Medical Systems (Cleveland) Inc

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Instrumentation Industries Inc: BE 183 Series Manual Jet Ventilators. Manual Jet Ventilator

possible external debris in the on/off plunger.

FDASep 12, 2003CA, FL, GA +6 more• Instrumentation Industries Inc

Weber Marking System Inc.: Weber SolarJet S CO2 Vector Laser Coder System; Weber Mar...

The laser product failed to comply with the performance standards, including certification, identification, warning logotype label, aperture label and submission of a product report.

FDASep 12, 2003VA• Weber Marking System Inc.

VIASYS Med Systems: Sideport Kit w/Oxygen Line, consisting of an adjustable s...

The exhalation hole in the sideport relief valve may be blocked, allowing excess pressure build-up.

FDASep 10, 2003AZ, CA, GA +10 more• VIASYS Med Systems

VIASYS Med Systems: Hyperinflation Circuit, consisting of a 2.0 L breathing b...

The exhalation hole in the sideport relief valve may be blocked, allowing excess pressure build-up.

FDASep 10, 2003AZ, CA, GA +10 more• VIASYS Med Systems

VIASYS Med Systems: Sideport Kit, consisting of an adjustable sideport valve ...

The exhalation hole in the sideport relief valve may be blocked, allowing excess pressure build-up.

FDASep 10, 2003AZ, CA, GA +10 more• VIASYS Med Systems

VIASYS Med Systems: Neonatal/Infant Hyperinflation Circuit, consisting of a 0...

The exhalation hole in the sideport relief valve may be blocked, allowing excess pressure build-up.

FDASep 10, 2003AZ, CA, GA +10 more• VIASYS Med Systems

Summit Gas Grills (Weber-Stephen) – Performance Issue (2003)

Fire/Burn Risk

The Summit Gas Grills are stainless steel and have model numbers 5210001, 5310001, 5220001, 5320001, 5230001, 5330001, 5260001, 5360001, 5270001, 5370001, 5290001, and 5390001, with serial numbers beginning with the letters DT. The model and serial number is located on the outside right panel of the storage cart. The Summit grills are sold as either a four-burner Silver series or six-burner Gold series. The private labeled Vieluxe Gas Grills have model numbers 360201, 360102, 370201, 370102 and 370299, with serial numbers beginning with the letters DA, DU, and DT. The model and serial number is located inside of the side access door on the right side of the grill. The grills are sold as either a four-burner 44-inch model or a six-burner 56-inch model, are made of high-grade stainless steel, and are equipped with a rear-mounted infrared burner and rotisserie device. Weber grills with a brand name other than Vieluxe or Summit are not included in this recall.

CPSCSep 10, 2003Nationwide• Weber-Stephen Products Co., of Palatine, Ill.

OnQ Telephone Devices (OnQ) – Line-Sharing Problem (2003)

The recalled units are labeled "OnQ" and "1x8 ENHANCED TELECOM w/SURGE." The devices are professionally installed as part of a telephone line-sharing system in homes. One of the slots on the device is labeled, "SECURITY." The security line should get priority in an emergency. Part number 364551-01, written on the product label, and a date code (DC) of "2303" (meaning the 23rd week of 2003) or earlier are included in the recall. The date code is located on the edge of the device, above the mounting tabs.

CPSCSep 10, 2003Nationwide• OnQ Technologies, of Middletown, Pa.

Easter Oil Lamps (DesignPac) – Glass Bottle Risk (2003)

Fire/Burn Risk

These lamps are oval glass bottles with purple or pink dots. They are filled with blue or pink liquid paraffin. The lamps were sold with bunny-shaped tags identifying them as "hoppy go lucky" oil lamps. Item number 054-03-1843 or 054-03-1844 is printed on the tag. Some of the lamps were sold with round metal disks meant to prevent the lamps from tipping.

CPSCSep 10, 2003Nationwide• DesignPac Inc., of Northlake, Ill.

Baby Walkers (SunTech) – Mobility Safety (2003)

The recalled baby walkers are made with a plastic frame supported by six or eight wheels on the bottom. The walkers are blue, pink or bright green, with a padded seat and an activity tray. "SUN KIDS" or "HAPPY BABY" labels appear on some of the walkers.

CPSCSep 10, 2003Nationwide• SunTech Enterprises Inc., City of Commerce, Calif.

Medtronic MiniMed: Ambulatory infusion pump. Model 511

Non delivery of insulin by pump after electrostatic discharge.

FDASep 9, 2003Nationwide• Medtronic MiniMed

Beckman Coulter Inc: Coulter AcT 5diff Cap Pierce Hematology Analyzers Part N...

Samples with high fat content will not count platelets accurately.

FDASep 8, 2003Nationwide• Beckman Coulter Inc

Beckman Coulter Inc: Coulter AcT 5diff Open Vial Hematology Analyzers Part Nu...

Samples with high fat content will not count platelets accurately.

FDASep 8, 2003Nationwide• Beckman Coulter Inc

Advanced Sterilization Products: Ortho-phthaladehyde Concentration Indicator Browne CID...

Performance failure complaints.

FDASep 4, 2003Nationwide• Advanced Sterilization Products

Advanced Sterilization Products: Gluteraldehyde Concentration Indicators ''Browne GA In...

Performance failure complaints.

FDASep 4, 2003Nationwide• Advanced Sterilization Products

Beckman Coulter Inc: Synchron Systems Acetaminophen Reagent, part No. 472169.

Firm shortened calibration frequency to 7 days from 14 days.

FDASep 4, 2003Nationwide• Beckman Coulter Inc

International Surgical Supply, Inc.: ETHICON brand surgical device with an added label with th...

Various Sterile Expired and Non-expired Ethicon brand surgical devices were resterilized without adequate validations and distributed.

FDASep 3, 2003IN, MN, TN• International Surgical Supply, Inc.