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All product recalls affecting Mississippi.
Includes nationwide recalls (tagged “Nationwide”) and recalls with Mississippi in the distribution area.
Thrombectomy device specifies vessel range of 2.5-6 mm on the pouch, carton, and Instructions for Use rather than the correct vessel range of 3-6 mm, which could incrementally increase the radial force on the artery, which has the potential of vascular complications.
Corp. Micro Bird, Inc. (Micro Bird) is recalling certain 2023 G5 transit buses. The u-bolts securing the suspension blades may break.
Harley-Davidson Motor Company (Harley-Davidson) is recalling certain Fairing Lowers installed on 2023-2025 Touring and CVO Touring, Inverted Forks installed on 2025 FLHXU, and Fairing Lowers and Inverted Forks kits installed on 2024-2025 FLHX and FLTRX motorcycles. These accessories may obstruct the visibility of the front and side reflectors. As such, motorcycles equipped with these accessories fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 108, "Lamps, Reflective Devices, and Associated Equipment."
Corp. Micro Bird, Inc. (Micro Bird) is recalling certain 2023 G5 school buses. The u-bolts securing the suspension blades may break.
White River Marine Group LLC (WRMG) is recalling certain 2024-2025 Tracker Marine Trailstar TRL and Topper boat trailers. The winch strap may fray after contacting the crossbar and break, allowing the boat to detach from the trailer.
ILJIN Hysolus (ILJIN) is recalling certain Compressed Natural Gas (CNG) tanks. For a complete list of part numbers, please see the attached document. The pressure relief device may not fully vent, which can cause the tank to rupture. As such, these tanks fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 304, "Compressed Natural Gas Fuel Container Integrity."
Due to a software issue, the software may incorrectly process the date of birth (DoB) received from the Laboratory Information System (LIS) and when the DoB is set to 01/01/1900 or left empty, REMISOL Advance may incorrectly identify a patient as a newborn, affecting the execution of validation rules based on incorrect reference ranges. The test results are not changed by this software defect and are accurately displayed by REMISOL Advance; however, the evaluation flagging of the results may be affected. This issue may lead to wrong reference range calculations and can result in erroneous flagged results being auto validated and uploaded to LIS.
Nova Bus (US) Inc. (Nova Bus) is recalling certain 2022-2023 LFS transit buses. The engine wiring harness may be the incorrect length, which can result in harness damage and a loss of drive power.
Incorrect labeling in which the front red pouch label did not match the actual size of the medical device. The label on the front of the scope incorrectly states 5.0/2.2 while the back label, shipping box and product inside correctly states 5.6/2.8.
A cybersecurity vulnerability was discovered through internal testing.
Vials of implant bone granules may contain less product then specified on labeling.
A cybersecurity vulnerability was discovered through internal testing.
Disconnection of the adapter from the endotracheal tube can potentially be difficult or not possible.
Apic Yamada has recently discovered that certain products may be out of compliance with FDA electronic product regulations in that they did not bear a required label.
Potential for microbial contamination.
Forest River, Inc. (Forest River) is recalling certain 2025 Coachmen Apex and Remote travel trailers. The solar panel wiring may be incorrectly wired to the battery, causing it to melt.
Potential for microbial contamination.
Preset treatment parameters are not consistently being used in accordance with the IFU.
Incorrect product packaged in INSPIRA AIR Balloon Dilation System carton.
The recall is being carried out because repacking methods pose a possible risk of contamination. Sealing methods are not heat-sealed.