Recalls affecting Missouri
Notices that name Missouri in their distribution area, plus every nationwide recall — nationwide recalls reach Missouri too.
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NHTSA safety recall · 1+ years ago
Toyota bZ4X, Lexus RZ and and Subaru Solterra recall: During certain HVAC system faults, such as electrical compressor failure
During certain HVAC system faults, such as electrical compressor failure, the defroster and defogger system may become inoperative.
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NHTSA safety recall · 1+ years ago
Chrysler Jeep Wagoneer S recall: The vehicles are equipped with an incorrect cross car beam in the instrument
The vehicles are equipped with an incorrect cross car beam in the instrument panel. As such, these vehicles fail to comply with the requirements of…
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NHTSA safety recall · 1+ years ago
Chrysler recall: A software error within the hybrid control processor may result in a loss
A software error within the hybrid control processor may result in a loss of drive power.
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NHTSA safety recall · 1+ years ago
Chrysler Dodge Charger and Jeep Wagoneer S electric recall: An incorrectly installed spring may cause the loss of the park function
An incorrectly installed spring may cause the loss of the park function when the vehicle’s gear selector is placed in the park (P) position, which…
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NHTSA safety recall · 1+ years ago
Chrysler Pacifica and Voyager recall: The right and left side curtain air bags may have insufficient pressure
The right and left side curtain air bags may have insufficient pressure retention from improperly sealed seams. As such, these vehicles fail to…
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Highest risk · 1+ years ago
StopBox USA AR-15 Chamber Lock Pros recall: Risk of Serious Injury and Death
Risk of Serious Injury and Death
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Highest risk · 1+ years ago
Makita U.S.A., Inc. Cordless Grease Guns and Grease Gun Hoses recall: Laceration Hazard
Laceration Hazard
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Class III · 1+ years ago
Philips Ultrasound, Inc X3-1 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class II · 1+ years ago
CareFusion 303, Inc. BD Pyxis Product Name / UDI-DI code / recall: Antivirus software was not consistently installed on impacted devices during
Antivirus software was not consistently installed on impacted devices during the implementation process.
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Class III · 1+ years ago
Philips Ultrasound, Inc S7-2t Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class III · 1+ years ago
Philips Ultrasound, Inc S12-4 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class III · 1+ years ago
Philips Ultrasound, Inc S8-3 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class III · 1+ years ago
Philips Ultrasound, Inc C9-5ec Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class II · 1+ years ago
Orascoptic Superior Visualization Phantom Essential kit recall: Due to complaints, loupe nose pads containing nickel may cause an allergic
Due to complaints, loupe nose pads containing nickel may cause an allergic reaction.
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Class III · 1+ years ago
Philips Ultrasound, Inc C10-3v Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class III · 1+ years ago
Philips Ultrasound, Inc L17-5 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class II · 1+ years ago
Orascoptic Superior Visualization Custom loupes configured with Phantom recall: Due to complaints, loupe nose pads containing nickel may cause an allergic
Due to complaints, loupe nose pads containing nickel may cause an allergic reaction.
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Class II · 1+ years ago
Onkos Surgical, Inc. Eleos Segmental Limb Salvage System recall: Unidentified substance of unknown impact was identified on devices during
Unidentified substance of unknown impact was identified on devices during a retrospective evaluation.
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Class III · 1+ years ago
Philips Ultrasound, Inc X7-2t Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class II · 1+ years ago
Onkos Surgical, Inc. Eleos Segmental Limb Salvage System recall: Unidentified substance of unknown impact was identified on devices during
Unidentified substance of unknown impact was identified on devices during a retrospective evaluation.
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Class III · 1+ years ago
Philips Ultrasound, Inc L15-7IO Transducer Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class III · 1+ years ago
Philips Ultrasound, Inc C5-2 Transducer Probe recall: To provide clarification and labelling to define the useful life
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
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Class II · 1+ years ago
C.R. Bard Inc Bardex Lubri-Sil I.C. 400-series Temperature Sensing Silver/Hydrogel recall: Foley catheter may have an obstructed lumen
Foley catheter may have an obstructed lumen, which may result in an inability to drain the bladder, of urine and may include pelvic or abdominal…
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Class II · 1+ years ago
Onkos Surgical, Inc. Eleos Segmental Limb Salvage System, Eleos Stem Extension recall: Unidentified substance of unknown impact was identified on devices during
Unidentified substance of unknown impact was identified on devices during a retrospective evaluation.