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All product recalls affecting Alaska.
Includes nationwide recalls (tagged “Nationwide”) and recalls with Alaska in the distribution area.
This recall involves the Momentum Vida E+ E-bike. The bicycles come in metallic red, pearl white, metallic navy blue, metallic green, indigo blue, happy mint (light green) and panther (black). The bicycle comes in two frame configurations (mid-step and low-step) and both configurations come in small, medium and large sizes. The unique serial number for each bike is stamped into the frame on the outer side of the left rear dropout and on a printed sticker under the bike's downtube. "Momentum" is written on the downtube of the bicycle and "Vida E+" is written on the top tube.
This recall involves Ozark Trail 64 oz Stainless Steel Insulated Water Bottles sold with model number 83-662 on the product packaging. The stainless-steel bottles are silver with a black one-piece screwcap lid. They measure 4.41 x 4.41 x 11.5 inches and there is an Ozark Trail logo embedded on the side of the bottle. The model number does not appear on the product.
FilmArray NGDS Warrior Panel (NGDS-ASY-0007) has an increased risk of internal control failures when testing positive blood culture, which may lead to delayed results and additional diagnostic workup.
CGMP Deviations; particulates identified during visual inspection
CGMP Deviations
CGMP Deviations; particulates identified during visual inspection
CGMP Deviations
CGMP Deviations
Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.
Mitsubishi Fuso Truck of America, Inc. (MFTA) is recalling certain 2024 Rizon FEC7K (E16), FEC9K (E18), and 2025 FECXK (E18) trucks. The electric parking brake (EPB) actuator may use a spacer that is too big, resulting in excessive friction and overheated brake components.
Reports of delayed access to medication in automated dispensing cabinets because of the override/Add Item workflow.
Access Thyroglobulin reagent lot 439163 may generate erroneously high patient results. Falsely increased Access Thyroglobulin results may lead a physician to pursue unnecessary diagnostic imaging studies and/or inappropriate therapy adjustments in patients being monitored for residual or recurrent thyroid cancer.
Airstream, Inc. (Airstream) is recalling certain 2025 - 2026 Interstate motorhomes. The Parametric Special Module (PSM) may fail to lock the controls, allowing the awning to be extended during transit.
Prevost Car (US) Inc. (Prevost) is recalling certain 2025 X3-45 and 2025-2026 H3-45 coach buses. The fasteners securing the passenger seat back or the seat belt may be loose.
Knee implants contain incorrect labeling
Generations 67 and above of VITROS Ca Slides are experiencing an increased occurrence of Condition Code TH4-63J during calibration on VITROS XT 3400 and VITROS XT 7600 Systems, causing calibration failures that delay calcium test results and potentially impact patient management. The imaging reflectometer algorithm detects excessive "spikes" (imperfections) in slide images and generates the TH4-63J condition code when the threshold of 600 spikes is exceeded. Updated analysis revealed a 19-fold increase in failure rates from 0.0043% (2024 baseline) to 0.082% for Generation 67+ slides in 2025, with 100% of calibrator failures occurring at the lowest concentration level. This can result in delayed diagnosis and treatment of conditions such as hypercalcemic crisis, parathyroid disorders, and other calcium-related emergencies requiring urgent intervention.
Subpotent Drug
Sub-Potent Drug: Subpotent assay results during stability testing.
CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above the FDA recommended acceptable intake limit.
Sub-Potent Drug: Subpotent assay results during stability testing.