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All product recalls affecting Tennessee.
Includes nationwide recalls (tagged “Nationwide”) and recalls with Tennessee in the distribution area.
This recall involves three models of SuperATV carrier bearings sold from April 2017 until September 2022 for installation in Polaris RZR XP Turbo or Turbo S vehicles. The recalled carrier bearings are silver and black and have "SuperATV" etched on top of the carrier bearing housing. The carrier bearing is located under the center console tunnel which is behind the seats on the two-seat model and behind the rear seats on the four-seat models. The following carrier bearing models are subject to this recall if purchased for the Polaris RZR XP Turbo or Turbo S vehicles in the identified date ranges: RECALLED CARRIER BEARING MODEL POLARIS RZR XP TURBO OR TURBO S PURCHASE DATE RANGE BEA01-001 4/13/17 through 4/27/19 BEA01-002 5/19/18 through 1/22/19 BEA01-005 (Rev A00 and A01) 1/25/19 through 9/2/22
This recall involves Electra Navigator Go! (Model years 2021 and 2022) and Electra Ace of Spades Go! e-bikes (Model years 2018, 2021 and 2022). The Electra Navigator Go! comes in Matte Nautilus Blue with map/ocean graphics and the Ace of Spades Go! comes in Matte Black with a gold spade. The name "Electra" is printed on the chain guard of the Navigator Go! with a compass on the top tube. The name "Electra" is printed on the down tube and chain guard of the Ace of Spades Go! with a spade on the top tube.
This recall involves model years 2024 and 2025 Triumph TF250-X closed course competition motorcycles. The black motorcycles have vehicle identification numbers (VIN) between BP6028 and CC7868 located on the left side of the steering head. "Triumph" is printed on the seats. Consumers can check if their VIN is included in this recall at https://www.triumphmotorcycles.com/owners/recalls.
Indian Motorcycle Company (Indian) is recalling certain 2025 Challenger Dark Horse, Pursuit Limited, Roadmaster Elite and Springfield Dark Horse motorcycles. Due to an incorrectly crimped wire, the fuel pump may fail and result in an engine stall during operation.
Marketed without an approved NDA/ANDA: Product found to be tainted with undeclared sildenafil and tadalafil.
Presence of Particulate Matter
There is a potential security vulnerability in Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000) where the service login credentials are able to be identified which could allow a malicious actor with these credentials to access the system and potentially manipulate patient data.
There is a potential security vulnerability in Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000) where the service login credentials are able to be identified which could allow a malicious actor with these credentials to access the system and potentially manipulate patient data.
In situations where two images with differing Fields of View (FOV) complete an image fusion, an incorrect, elevated Maximum Standardized Uptake Value (SUV) within MIM Software versions 7.2.0 through 7.2.6.could result.
When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements may be inconsistent with the associated primitive measurements in the final patient report.
Aspiration system, for endoscopic examination/treatment of urinary tract and kidney interior, to have labeling update adding additional instructions, for patients with high viscosity fluid in the kidney, not to continue providing fluid inflow in the presence of unresolved slow or absent fluid outflow because this can create intrarenal pressure imbalance, and lead to excessive intrarenal pressure.
There is a potential security vulnerability in Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000) where the service login credentials are able to be identified which could allow a malicious actor with these credentials to access the system and potentially manipulate patient data.
Volvo Car USA, LLC (Volvo) is recalling certain 2025 S90 vehicles. The windows may be improperly secured and detach.
There is a potential security vulnerability in Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000) where the service login credentials are able to be identified which could allow a malicious actor with these credentials to access the system and potentially manipulate patient data.
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2022-2024 Golf GTI vehicles. A software error may delay or deactivate the rearview camera image, resulting in the rearview camera image not displaying as intended. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 111, "Rear Visibility."
There is a potential security vulnerability in Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000) where the service login credentials are able to be identified which could allow a malicious actor with these credentials to access the system and potentially manipulate patient data.
Nova Bus (US) Inc. (Nova Bus) is recalling certain Casco engine coolant level sensors with part number N108036. The coolant sensor could send a false signal, causing the engine to shut down.
Lazervida 10W Diode Laser Engraver does not fully meet current Federal performance standards in certain areas. Specifically, the product does not incorporate the additional beam attenuator, remote interlock connector, key switch, specific labels and manual instructions required under current regulations.
There is a potential for the sterility of the device to be compromised.
When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical Reporting, derived measurements may be inconsistent with the associated primitive measurements in the final patient report.