Recalls affecting Vermont
Notices that name Vermont in their distribution area, plus every nationwide recall — nationwide recalls reach Vermont too.
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NHTSA safety recall · 8 months ago
Ford Explorer and Lincoln Aviator recall: The seat belt anchor bolts at the second-row outer seating positions
The seat belt anchor bolts at the second-row outer seating positions may be improperly secured.
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NHTSA safety recall · 8 months ago
Chrysler Jeep Wagoneer S recall: The liftgate hinge cover may not be properly clipped into position
The liftgate hinge cover may not be properly clipped into position and may detach from the vehicle.
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Highest risk · 8 months ago
Stoney Games Kluster Magnet Chess Games recall: Risk of Serious Injury or Death from Magnet Ingestion
Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys
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Highest risk · 8 months ago
ProRider Bicycle Helmets recall: Risk of Serious Injury or Death from Head Injury
Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets
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Elevated risk · 8 months ago
Lfte USA Playground Swing Set Seats recall: Fall Hazard
Fall Hazard
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NHTSA safety recall · 8 months ago
Volvo Car EX30 and EX30CC recall: The seat belt warning system may not activate the audible warning chime
The seat belt warning system may not activate the audible warning chime as intended. As such, these vehicles fail to comply with the requirements of…
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NHTSA safety recall · 8 months ago
Volkswagen Jetta recall: The transmission ground wire may not have been properly connected during
The transmission ground wire may not have been properly connected during assembly, causing an open electrical circuit.
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Class II · 8 months ago
Olympus Corporation of the Americas Brand Name: ShockPulse-SE Lithotripsy System recall: Ongoing investigations identified additional instances of the device
Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer…
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Class II · 8 months ago
Vascutek, Ltd. Gelsoft Plus, REF: 635024PE, 631514PE, 631222PE, 633008PE recall: Gelatin sealed woven polyester prostheses devices
Gelatin sealed woven polyester prostheses devices, designed for vascular repair, were incorrectly labeled with an additional month of shelf life…
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Class II · 8 months ago
Diagnostica Stago, Inc. Brand Name: STA Liatest Free Protein S Product Name: STA recall: The potential of out-of-range results and an underestimation of the free
The potential of out-of-range results and an underestimation of the free protein S level in normal patient plasmas. The defect only affects…
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Class II · 8 months ago
Olympus Corporation of the Americas Brand Name: ShockPulse-SE Lithotripsy System recall: Ongoing investigations identified additional instances of the device
Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer…
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Class II · 8 months ago
B Braun Medical Inc Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM recall: The potential for the needle tip to be dull/blunt
The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
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Class II · 8 months ago
B Braun Medical Inc Brand Name: B. Braun Product Name: 21GA Winged Infusion recall: The potential for the needle tip to be dull/blunt
The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
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Class II · 8 months ago
Datascope Corp. CS100 Iabp. Software Version CS100 Iabp Q.01 recall: The firm has identified that the battery runtime and cycle specifications
The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.
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Class II · 8 months ago
Siemens Healthcare Diagnostics, Inc. Atellica CH Urine Albumin . Material Number recall: Falsely depressed UAlb patient results may occur. Affected samples with any
Falsely depressed UAlb patient results may occur. Affected samples with any urine albumin concentration above the UAlb measuring interval >40.0 mg/dL…
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Class II · 8 months ago
Datascope Corp. CS300 Iabp. Software Version CS300 Iabp C.01 recall: The firm has identified that the battery runtime and cycle specifications
The firm has identified that the battery runtime and cycle specifications contained in the devices Instructions for Use (IFU) need to be updated.
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Class II · 8 months ago
GE Healthcare GE Healthcare Centricity Universal Viewer Zero Footprint Client recall: Under certain workflows, patient information shown in the viewer
Under certain workflows, patient information shown in the viewer may not match the images displayed on Centricity Universal Viewer Zero Footprint…
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Class II · 8 months ago
Roche Diagnostics Operations, Inc. cobas pro integrated solutions with cobas c 503 recall: Software defect, which allows the system to accept erroneous
Software defect, which allows the system to accept erroneous, non-monotonous calibrations for Spline-type assays. Cobas pro integrated solutions is…
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Class II · 8 months ago
Esaote Endocavity ultrasonic probe, Model E 3-12, REF 120000038 recall: A potential weakness has been identified in the probe body
A potential weakness has been identified in the probe body, so that, in a specific production batch, liquid may leak from the terminal part of the…
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Class II · 8 months ago
Brand Name: Aesculap Product Name: Minop Trocar 150MM 4 Wking recall: There is the potential for the length of the trocar shaft to be too long
There is the potential for the length of the trocar shaft to be too long.
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Class I · 8 months ago
Abiomed, Inc. Impella RP. Product Code: 0046-0011 recall: Differential pressure (dP) sensor in Impella RP devices may malfunction
Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.
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Class II · 8 months ago
B Braun Medical Inc Brand Name: B. Braun Product Name: 21GA Winged INF SET Model/ recall: The potential for the needle tip to be dull/blunt
The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
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Class II · 8 months ago
Olympus Corporation of the Americas Brand Name: ShockPulse-SE Lithotripsy System recall: Ongoing investigations identified additional instances of the device
Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer…
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Class I · 8 months ago
Abiomed, Inc. Impella RP with SmartAssist. Product Code: 0046-0035 recall: Differential pressure (dP) sensor in Impella RP devices may malfunction
Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.