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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

582

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 8981–9000 of 10937 recalls

Medtronic Xomed, Inc.: Medtronic Integrated Power Console System, IP X1 REF 189...

An error code (Code 13) is displayed on some of the consoles when a Medtronic Stylus or EHS handpiece is connected to the IPC indicating that the handpiece has not been recognized by the console.

FDAJul 17, 2009Nationwide• Medtronic Xomed, Inc.

Draeger Medical Systems, Inc.: Stabilet Infant Warming System, model numbers 200, 300, 1...

Fire/Burn Risk

Hot particles fell into the infant bassinet beneath a Radiant Infant Warmer. The resulting fire injured an infant. These devices are obsolete.

FDAJul 17, 2009Nationwide• Draeger Medical Systems, Inc.

Impac Medical Systems Inc: SEQUENCER component of MOSAIQ versions 1.30 (all builds),...

Potential for improper treatment. A software error may result in potential major underdosing to targeted areas from jaw blockage of the MLC aperture (jaw intrusion), and dosing to non-targeted areas from interstitial leaf leakage (jaw extrusion).

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FDAJul 17, 2009AL, CA, CT +19 more• Impac Medical Systems Inc

Varian Medical Systems Oncology Systems: Varian Medical Systems, Eclipse Proton Convolution Superp...

Software Issue/Mistreatment Potential-- Due to software issues, dose distribution may be incorrect and unintended radiation doses may be delivered.

FDAJul 17, 2009IN, TX• Varian Medical Systems Oncology Systems

Switch-A-Roo Telephone Toys (Evenflo) - Choking Risk (2009)

Choking Hazard

The recall involves Evenflo Switch-A-Roo telephone toys made between October 2008 and June 2009. The model number is 6391911.

CPSCJul 16, 2009Nationwide• Evenflo Co. Inc., of Miamisburg, Ohio

Steritec Products Mfc. Co., Inc.: Plasma Chemical Sterilization Indicator. Product Numbers ...

This action notifies affected SteriTec customers as well as private label distributors of the necessity to modify the shelf life of their products. There is insufficient data on file to support the shelf life dating on the product labeling.

FDAJul 15, 2009Nationwide• Steritec Products Mfc. Co., Inc.

Steritec Products Mfc. Co., Inc.: Violet Ink sterilization indicators Violet Ink (Class 6) ...

This action notifies affected SteriTec customers as well as private label distributors of the necessity to modify the shelf life of their sterilization indicator products. There is insufficient data on file to support the shelf life dating on the product labeling.

FDAJul 15, 2009Nationwide• Steritec Products Mfc. Co., Inc.

Toshiba American Medical Systems Inc: Whole Body X--ray Scanner This device is indicated as a ...

1. It has been found that in raw data processing for Go&Return helical scanning, when the raw data acquired in the first scan (Go) and that acquired in the second scan (Return) are selected and reconstructed at one time, incorrect couch positions and scan times are displayed on the reconstructed images for the data acquired by Return scanning, while all related information is displayed on the reco

FDAJul 13, 2009Nationwide• Toshiba American Medical Systems Inc

Toshiba American Medical Systems Inc: Whole Body X--ray Scanner This device is indicated as ...

Class IIModerate

FDAJul 13, 2009Nationwide• Toshiba American Medical Systems Inc

Kidde Smoke Alarms (Walter Kidde) - Fire Warning Failure (2009)

Fire/Burn Risk

This recall involves Kidde dual sensor smoke alarms model PI2000. The alarms can be identified by two buttons, "HUSH" and "PUSH AND HOLD TO TEST WEEKLY," which are located on the front/center of the alarm. The model number and date code are on the back of the smoke alarm. Only date codes 2008 Aug.01 through 2009 May 04 are included in this recall.

CPSCJul 9, 2009Nationwide• Walter Kidde Portable Equipment Inc., of Mebane, N.C.

Mosquito Traps (BioSensory) – Laceration Risk (2009)

Fire/Burn Risk

The Dragonfly II Model 503 is a cylindrical unit made of metal and plastic with a black, silver and dark graphite finish. The units are about 36 inches tall and 8 inches in diameter. The Dragonfly logo, model number, electrical information, Canadian Standards Association (CSA) mark for Canada and the United States (C US), BioSensory street and internet address are engraved on the main housing, on the side opposite the control panel. The NightWatch Model 506 is a white molded plastic unit 14 inches long and 6 inches high with a black and white striped thermal lure over the top and sides. Two detachable pitfalls are on either side of the unit. The pitfalls have a felt ramp leading to the elongated collection pit. The NightWatch model number, electrical information, Canadian Standards Association (CSA) mark for Canada and the United States (C US), BioSensory street and internet address are engraved on the underside of the unit beneath the control panel.

CPSCJul 7, 2009Nationwide• BioSensory, Inc., of Putnam, Conn.

Becton Dickinson & Company: BD 60ml Syringe Luer-Lok tip, Sterile, BD, Franklin Lakes...

Insufficient Seal: Becton Dickinson received complaints of insufficient/open seals on one lot of 60 ml Luer-Lok Syringes.

FDAJul 7, 2009Nationwide• Becton Dickinson & Company