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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

583

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 9861–9880 of 10937 recalls

Medtronic Xomed, Inc.: AccuGuide Injection Needles (Surface electrodes) The A...

A labeling discrepancy was internally identified for the surface electrode component of REF 8263210 AccuGuide EMG Injection Needle, 30G X 25MM. The outside box label correctly indicates 'Content: 5 sterile Injection Needles and 10 non-sterile Surface electrodes'; however, the pouches for the 10 surface electrodes inside the box are incorrectly labeled as 'sterile'.

FDAJan 22, 2007Nationwide• Medtronic Xomed, Inc.

Next Step Sippy Cups (Artcraft) – Laceration Risk (2007)

Laceration Risk

This recall involves plastic sippy/tumbler cups bearing the "Next Step" logo. The 7-ounce cup has an aqua blue cap and a yellow, rubber-like material covering the handles and bottom of the cup.

CPSCJan 22, 2007Nationwide• Artcraft and Foremost Inc., of Moorestown, N.J.

Weil-McLain Boilers – Carbon Monoxide Risk (2007)

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The recall involves the Weil-McLain Model 80, 88, 94, and LGB Packaged Commercial Boilers built from December 1, 2005 through October 26, 2006. The model information is written on a name plate or rating label on the front blue sheet metal jacket panels.

CPSCJan 22, 2007Nationwide• Weil-McLain Co., of Michigan City, Ind.

Clark Research and Development Inc Number: Clark Biocompatible Hemoperfusion Cartridge, Sorbent: He...

Lack of sterility assurance based on lack of sterility validation for labeled sterilization directions

FDAJan 19, 2007Nationwide• Clark Research and Development Inc Number

Smiths Medical MD, Inc.: Deltec branded CADD-Prizm PCS II ambulatory infusion pump...

The year of manufacture had been incorrectly entered as 1980 into the pumps software during the manufacture process. As a result the pump may go into an immediate 'Clock battery is Low/Service Immediately' or 'Clock Battery needs service soon' alarm message indicating that the pump requires servicing.

FDAJan 19, 2007Nationwide• Smiths Medical MD, Inc.

GE OEC Medical Systems, Inc: OEC Uroview 2800 fluoroscopic x-ray system with 3 Phase P...

Uroview 2800 system with 3 Phase Power Distribution Box (Wonder Box) option can present a shock hazard to the user if the access door to the power box is not completely closed when the unit is powered on. .

FDAJan 15, 2007Nationwide• GE OEC Medical Systems, Inc

GE OEC Medical Systems, Inc: OEC Uroview 2800 with Dual Monitor Option, fluoroscopic x...

Uroview 2800 system with dual monitors may pose a safety risk to patients if the monitors become disconnected and fall.

FDAJan 15, 2007Nationwide• GE OEC Medical Systems, Inc

Terumo Cardiovascular Systems Corp: Terumo Perfusion System 8000 Base, 4 pump, 115v; Model 80...

The hand crank may crack in the bearing/shaft area due to a manufacturing defect. (Note: Some of the hand cranks subject to this recall were shipped as replacements for hand cranks recalled in the Summer of 2006.)

FDAJan 12, 2007Nationwide• Terumo Cardiovascular Systems Corp

Philips Medical Systems (Cleveland) Inc: No packaging. The device is a computed tomography scanne...

When the Extended Display Firled ov View reconstruction is used, the CT numbers and anatomy in teh extended region are not accurate.

FDAJan 9, 2007AR, CA, FL +16 more• Philips Medical Systems (Cleveland) Inc

Philips Medical Systems (Cleveland) Inc: No packaging. The device is a computed tomography scanne...

When the Extended Display Firled ov View reconstruction is used, the CT numbers and anatomy in teh extended region are not accurate.

Class IIModerate

FDAJan 9, 2007AR, CA, FL +16 more• Philips Medical Systems (Cleveland) Inc

Gas Pool Heaters (Pentair) – Carbon Monoxide Danger (2007)

The recall involves Pentair MiniMax® NT STD Gas Pool Heaters installed indoors. They have BTU ratings between 200,000 and 400,000, and use either natural gas or propane. The model number is located on the rating plate on the inner front panel of the heater. The following model numbers are included: 460427 through 460430 460439 through 460450 460531 through 460538 460543 through 460566 The heater identification number is located on the rating plate on the inner panel of the heater, which will show "NT" and "STD" in the third and fourth blocks of the number. The recall includes units with serial numbers 0606002 and lower. The recall also includes units without serial numbers. If the unit has a serial number, it is written on the data plate on the heater, which is located on the inner front door of the heater. Units with serial number 0606003 and higher are not included in this recall. MiniMax® NT Low NOx and MiniMax® NT TSI model pool heaters are not included in this recall.

CPSCJan 4, 2007Nationwide• Water Pool and Spa Inc., of Moorpark, Calif.

Portable Generators (DEWALT) – Electric Shock Risk (2007)

The recall involves DEWALT DG2900 2900-watt gasoline-powered generators with date codes 200150 through 200635. The generators are black and yellow. "DEWALT" and "DG2900" are printed on the generator. The date code is stamped on the right side of the unit on the black plastic covering the rear of the control panel. Units with an "R" stamped on the name plate are not affected by this recall.

CPSCJan 4, 2007Nationwide• DEWALT Industrial Tool Co., of Towson, Md.

Medtronic Perfusion Systems: Medtronic 2T10R1 Intersept Custom Tubing Pack. Pack 2T...

One lot of Custom Perfusion Sets, Catalog 2T10R1 was incorrectly assembled. The one way vacuum relief valve on the 102 inch line is attached backwards, thus preventing flow.

FDAJan 2, 2007IL• Medtronic Perfusion Systems

Becton Dickinson and Company: BD Beaver Mini-Blade, Blade Sharp Two Sides Pointed, Cat...

Product sterility may be compromised due to incomplete package seal

FDADec 26, 2006Nationwide• Becton Dickinson and Company

Becton Dickinson and Company: BD Beaver Mini-Blade, Mini/Bulk 64, Catalog Number: 374820

Product sterility may be compromised due to incomplete package seal

FDADec 26, 2006Nationwide• Becton Dickinson and Company

Becton Dickinson and Company: BD Beaver Mini-Blade, Blade Mini Orthopedic 1.255 in, Cat...

Product sterility may be compromised due to incomplete package seal

FDADec 26, 2006Nationwide• Becton Dickinson and Company

GE Medical Systems LLC: Definium AMX 700 Digital mobile x-ray system, GE Healthca...

When using the Tech Switch on exposures >750ms, >100 kVp and > 100 mAs the exposure terminates prematurely.

FDADec 21, 2006IN, MS, NE +2 more• GE Medical Systems LLC

Reciprocating Saws (DEWALT) – Fire Hazard (2006)

Fire/Burn Risk

This recall involves cordless DEWALT DC305 model reciprocating saws with date codes 200601-49 through 200640-49. They are yellow and black and about 18 inches long. The model number is located on the name plate on the side of the housing and the date code is located under the handle where the battery is inserted.

CPSCDec 21, 2006Nationwide• DEWALT Industrial Tool Co., of Towson, Md.

Cut-Out Tools (DEWALT) – Shock Hazard (2006)

Laceration Risk

These DEWALT cut-out tools are yellow and black, and have model number DW660 written on their nameplate, which is located on the body of the unit. The recalled tools were manufactured between January 2006 and September 2006, and have date codes ranging from 200601 to 200639. The date code also is located on the tool's nameplate. Units with a "V" stamped on the nameplate are not included in this recall.

CPSCDec 21, 2006Nationwide• DEWALT Industrial Tool Co., of Towson, Md.

Toshiba American Med Sys Inc: Nemio XG, ultrasound system, SSA-590A with version 1.5 so...

Transducer Surface Temperature : It was found during testing that when using the system in the 2DCDI + PW mode, with the Scale Graph function active, that the transducer surface temperature could exceed the 27 degrees Celsius limit as specified in the IEC safety standard.

FDADec 19, 2006Nationwide• Toshiba American Med Sys Inc