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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

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 20281–20300 of 21319 recalls

OEC Medical Systems, Inc: InstaTrak 3500 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

OEC Medical Systems, Inc: ENTrak 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: ENTrak 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.

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FDA

Dec 13, 2004

Nationwide

• OEC Medical Systems, Inc

OEC Medical Systems, Inc: InstaTrak 3000 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: 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

Ethicon Endo-Surgery: Mammotome EX Holster

A capacitor of the wrong value was used. The capacitor used was 0.11 microfarad instead of 0.22 microfarad called for in the product specifications.

FDADec 10, 2004AL, AR, CA +27 more• Ethicon Endo-Surgery

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.

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

Bio-Med Devices, Inc.: Bio Med Devices Patient Breathing Circuit Catalog Numbe...

Adapters may be occluded potentially preventing inhalation

FDADec 6, 2004Nationwide• Bio-Med Devices, Inc.

Bio-Med Devices, Inc.: Bio-Med Patient Breathing Circuit Product NUmber: 3030-5...

Adapters may be occluded potentially preventing inhalation

FDADec 6, 2004Nationwide• Bio-Med Devices, Inc.

Lazer Z Zero Turn Mowers (Exmark) – Engine Fire Risk (2004)

Fire/Burn Risk

The 2004 Model Lazer Z zero-turn (ZRT) riding mowers with 60-inch and 72-inch decks are equipped with electric fuel injection engines as follows: Model Serial Range Description Suggested Retail Price LZ28KC604 440000-500539 28HP ZRT w/60" deck $11,099 LZ28KC724 440000-500612 28HP ZRT w/72" deck $11,432 All products are equipped with a foldable roll-over protection bar. The model and serial number decal can be found on the frame below the seat.

CPSCDec 6, 2004Nationwide• Exmark Manufacturing of Beatrice, Nebraska

Bio-Med Devices, Inc.: Pneumotach, Disposable (B) Catalog Number: 4408 Labeled...

Adapters may be occluded potentially preventing inhalation

FDADec 6, 2004Nationwide• Bio-Med Devices, Inc.

Bio-Med Devices, Inc.: Bio-Med Dental Breathing Circuit Product NUmber: DENTL

Adapters may be occluded potentially preventing inhalation

FDADec 6, 2004Nationwide• Bio-Med Devices, Inc.

HK Surgical Inc: Gold Hub Capistrano Cannula, Catalog Nos. HK10C15; HK10C2...

Risk of hubs becoming disconnected from the cannula.

FDADec 3, 2004Nationwide• HK Surgical Inc

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.