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OEC Medical Systems, Inc

OEC Medical Systems, Inc Recalls

All product recalls associated with OEC Medical Systems, Inc.

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Recall Summary

Total Recalls

1000

Past Year

620

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 10421–10440 of 10937 recalls

OEC Medical Systems, Inc: InstaTrak 3500 Navigation and Visualization System

Enhanced sterility testing revealed the sterilization efficacy of accessories ('Sensors') used with certain Navigation and Visualization systems may be compromised.

FDADec 13, 2004Nationwide• OEC Medical Systems, Inc

OEC Medical Systems, Inc: FluroTrak 9800 Plus Navigation and Visualization System

Enhanced sterility testing revealed the sterilization efficacy of accessories ('Sensors') used with certain Navigation and Visualization systems may be compromised.

FDADec 13, 2004Nationwide• OEC Medical Systems, Inc

3-Way Compact Fluorescent Bulbs – Potential Malfunction (2004)

Fire/Burn Risk

The recalled 32-watt, 3-way (40-75-150 watt output) compact fluorescent bulbs were sold under the brand names Commercial Electric (Home Depot) and DuraBright (Orchard Supply Hardware). The bulbs are about seven inches high and have a white, spiral fluorescent tube attached to a white plastic base. The following item numbers, which can be found on the back of the packaging and the base of the bulb, are included in the recall: 283-924, 575-717, and 69032.

1...520 521522523 524...547

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CPSCDec 8, 2004Nationwide• Technical Consumer Products Inc., of Aurora, Ohio

Polaris Snowmobiles – Mechanical Failure (2004)

Fire/Burn Risk

Model year 2005 Polaris "900 Fusion" and "900 RMK 151" snowmobiles with model numbers S05MP8DS(A)(B)(C) and S05PL8DSA are part of this recall. The model number is located on the vehicle identification tag, located on the right side near the foot rest. The "900 Fusion" and "900 RMK 151" snowmobiles have either red/black or blue/silver/black seats with a red, black, or blue hood. "Fusion 900" or "RMK 900" is prominently displayed on the sides of the body.

CPSCDec 7, 2004Nationwide• Polaris Industries, Inc., of Medina, Minn.

Smiths Medical MD, Inc.: Deltec branded Administration Sets for use with Deltec 30...

Administration Sets which are used with selected infusion pump systems may have a defect within the fluid path above the upper chamber of the set cassette which does not allow the pump valve to close completely and can allow fluid to leask past and may cause an inaccurate infusion rate..

FDADec 3, 2004Nationwide• Smiths Medical MD, Inc.

Dade Behring Inc. Rte 896, Glasgow Business Community: Advanced D-Dimer. Fibrinogen and fibrin split products Ca...

decrease in product stability after reconstitution and reduced stability on board certain instrument systems

FDADec 3, 2004Nationwide• Dade Behring Inc. Rte 896, Glasgow Business Community

Philips Medical Systems Sales & Service Region No. America: Thoravision I Thorax and Mass Chest Column. Part numbers...

X-Ray system may fall downward and could possibly hit the patient.

FDADec 1, 2004Nationwide• Philips Medical Systems Sales & Service Region No. America

Philips Medical Systems Sales & Service Region No. America: Thoravision II Thorax and Mass Chest Column. Part number...

X-Ray system may fall downward and could possibly hit the patient.

FDADec 1, 2004Nationwide• Philips Medical Systems Sales & Service Region No. America

Northwest Medical Physics Equipment Inc: ISOLOC Software Version 4.2, Part Number NT-NW-425-520. ...

When ISOLOC Version 4.2 unit is set to centimeter and the user clicks the Reenter button in the digitizer window, the coordinates of the markers and target in the anatomic imaging system erroneously displays values ten times greater than the correct values.

FDANov 30, 2004Nationwide• Northwest Medical Physics Equipment Inc

Falls-Creek Children's Snow Suits – Safety Risk (2004)

Choking Hazard

The children's snow suits and jackets were sold in children's sizes 2T through 5T and 12M through 24M under the brand name, "Falls-Creek®." The two-piece snow suits included a jacket and overalls. Both clothing items have a small compass attached to the front of the jackets and were manufactured in a variety of colors. The care label bears RN# 48711.

CPSCNov 26, 2004Nationwide• Meijer Distribution Inc., of Grand Rapids, Mich.

Lakewood Mini-Personal Heaters – Fire Hazard (2004)

Fire/Burn Risk

The electric heater is a small white plastic heater with these dimensions: 6 x 7 x 3 inches. It has a gray grill and a gray knob. The Lakewood logo appears in gray letters on top of the heater. The model number "MPH-25" is embossed or appears on a sticker label on the bottom of the heater.

CPSCNov 23, 2004Nationwide• Lakewood Engineering & Manufacturing Company of Chicago, Illinois

Edwards Lifesciences Research Medical Inc: EMBOL-X Slim Access Device / Aortic Cannula 24 Fr X 11''.

Aortic cannula may delaminate and leak where it is bonded to the tip. This could occur during cardiopulmonary bypass surgery.

FDANov 19, 2004AL, CA, CO +21 more• Edwards Lifesciences Research Medical Inc

TriLite Stool (Byer) – Stability Issue (2004)

This recall includes Byer of Maine TriLite Stools shipped between February 19, 2004 and June 16, 2004. The affected stools are only those that have been produced in China, specifically those that bear the Byer of Maine logo screen printed in silver ink on the plastic leg hub.

CPSCNov 19, 2004Nationwide• The Byer Manufacturing Company, of Orono, Maine

Meter Socket Load Center (Midwest) – Electrical Risk (2004)

Fire/Burn Risk

The following models are included in this recall: model numbers R256EB1A, R256EB1NA, and R256EB1018A (Midwest) and TSLR1220CSAL (GE). Affected date code range is SAL421 through 432.

CPSCNov 19, 2004Nationwide• Midwest Electric Products, HW 22 North, Mankato, MN 56001

Pulmonetic Systems, Inc.: Universal Cable Adaptor (Part #17765-001 and labeled on o...

Reports have been received indicating that the Universal Cable Adaptor, intended to correct an earlier Class I recall of LTV Series Ventilators due to their inability to continue operating when external power source is switched to internal battery, is not functioning as intended and/or the cable is not securely attaching to the connection on the ventilator.

FDANov 19, 2004Nationwide• Pulmonetic Systems, Inc.

Hitachi Medical Systems America Inc: Altaire, Magnetic Resonance Imaging Device.

The absorber unit in the helium compressor which is located in equipment rooms, and is not accessed by patients or system operators, may fail under pressure, causing an explosion that damages the compressor.

FDANov 18, 2004AL, AZ, AR +34 more• Hitachi Medical Systems America Inc

Dade Behring Inc. Rte 896, Glasgow Business Community: StreamLab Analytical Workcell. General Purpose Laboratory...

Software can sample the incorrect specimen from the StreamLAB to the Dimension RxL or RxL Max Systems.

FDANov 12, 2004IL, IN, MD +3 more• Dade Behring Inc. Rte 896, Glasgow Business Community

B & K Medical Systems Inc.: Linear Array Transducer Type: 8809

Defect at probe tip may effect sterilization and electrical safety

FDANov 12, 2004CA, CO, CT +7 more• B & K Medical Systems Inc.

Smiths Medical MD, Inc.: Deltec branded PORT-A-CATH II Single-Lumen Low Profile Po...

The catheter became disconnected from the port while implanted in the patient.

FDANov 11, 2004FL, GA, IN +8 more• Smiths Medical MD, Inc.

Alaris Medical Systems Inc: Model 8100 Series Medley Medication Safety System Pump Mo...

The device modification is being implemented in response to information received from the field regarding a specific method of misloading the medication administration tubing set into the infusion system pump module. To date there have been complaints from three (3) different customer locations.

FDANov 10, 2004Nationwide• Alaris Medical Systems Inc