Willy Rusch Tracheostomy Tube Set by TeleFlex Medical: Class I Recall – Possible Disconnection During Patient Use Teleflex is recalling the Willy Rusch Tracheostomy Tube Set due to the possibility that the connector may disconnect from the tracheostomy tube during use on
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Target has recalled LED gel clings that can separate and expose the inner decal and LED/button battery compartment, posing choking and button battery ingestion hazards to children. This recall involves about 127,000 units, which were sold at Target stores nationwide from August
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The lower blade guard of the Makita 5057KB 7-1/4” circular saw with dust collector can malfunction and expose the blade, posing a laceration hazard and risk of injury to the consumer. This recall affects about 450 units, including the following serial number
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Cabela’s has recalled food dehydrators that were sold in its stores and on Cabelas.com from August 2016 through September 2016. Due to defective wiring, the dehydrators can become extremely hot posing a risk of fire. This recall affects about 3,000 stainless steel
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This recall involves Husqvarna®, Poulan Pro®, Jonsered®, Craftsman®, Yardworks®, Murray®, and Brute® brand walk-behind gas powered lawn mowers with Briggs & Stratton 7.25 HP engines. The operator presence control bar can malfunction and cause the engine and blades to continue to operate
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TUSA has recalled diving computers due to drowning and injury hazards. Tabata USA Inc.’s (TUSA) dive computer can malfunction and display an incorrect reading to a diver, which poses a risk to the diver of drowning or decompression sickness. This recall involves
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3 Squares Rice and Slow Cooker’s improperly installed wiring can cause electrical shorting in the unit, posing fire and electric shock hazards. If you own one of these rice/slow cookers it should immediately be replaced. About 175,000 units have been sold nationwide
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Medtronic has issued a voluntary recall of its Pipeline Embolization Device, Alligator Retrieval Device, X-Celerator Hydrophilic Guidewire, Ultraflow and Marathon Flow Directed Micro Catheters due to the potential separation and detachment of the polytetrafluoroethylene (PTFE) coating on parts of these devices. Should
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The Leonhard Lang defibrillation electrode is being recalled due to a connector compatibility issue with the Welch Allyn AED model 10. The Leonhard Lang defibrillation electrode is being recalled because the user may not be able to connect the electrodes when a
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St. Jude Medical Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) are devices that can pace slow heart rhythms, and also provide electrical shock to stop dangerously fast heart beats. These products have been affected due to premature battery failure.
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