Latest Product Recalls Today

US Truck Body Co., Inc. (US Truck Body) is recalling certain 2025 Isuzu NPR HD vehicles equipped with Waltco MDV series liftgates. The deck pins may break, causing the liftgate platform to fall. A liftgate that falls unexpectedly increases the risk of injury.

Jayco, Inc. (Jayco) is recalling certain 2027 Jayco Eagle, Eagle SLE, and Heartland Sundance fifth wheel trailers. The auto leveling jacks may be lowered during transit. Activation of the jacks during transit increases the risk of a crash.

Mack Trucks, Inc. (Mack) is recalling certain 2025 TerraPro trucks. The steering gearbox fasteners may loosen. A loose steering gearbox can result in a loss of steering, increasing the risk of a crash.

Chrysler (FCA US, LLC) is recalling certain 2023-2025 Dodge Hornet and 2023-2026 Alfa Romeo Tonale vehicles. The rear outboard seat belts may become twisted and fail to retract properly. A seat belt that does not retract may fail to restrain properly an occupant as intended, increasing the risk of injury.

Chrysler (FCA US, LLC) is recalling certain Mopar seat belt assemblies with part number 7SU27DX9AA, 7SU10DX9AA, 7SV41DX9AA, 7SV42DX9AA, 7ZK68DX9AA, 7ZK69DX9AA, 8AR89DX9AA, or 8BM60DX9AA. The rear outboard seat belts may become twisted and fail to retract properly. A seat belt that does not retract properly may fail to restrain an occupant as intended, increasing the risk of injury.

Tesla, Inc. (Tesla) is recalling certain 2017-2023 Model 3 and 2020-2023 Model Y vehicles. The headlight low beams may be too bright and exceed the maximum light output. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 108, "Lamps, Reflective Devices, and Associated Equipment." Headlight low beams that are too bright can reduce visibility for oncoming drivers, increasing the risk of a crash.

Firm's finished product label does not declare the source of marine collagen which was determined to be fish.

Products may be contaminated with Listeria monocytogenes.

Foreign material found in product (identified as metal shavings)

Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.

Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking and/or cracking at the hub, which may lead to replacement, inability to flush/aspirate catheter, catheter occlusion, therapy interruption, blood loss, tissue irritation, bloodstream infection.

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

Pinhole leaks may occur in the wire-wound body during cardiopulmonary bypass. Potential risks associated with this condition may include hypovolemia, vessel laceration or perforation, hypotension, ischemia, and organ dysfunction.

Potential for Bar Code Reader (BCR) wands, used with the GEM Premier 5000 and GEM Premier 7000 systems, to assign patient results to an incorrect patient ID.

The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the products.

Windstone Medical Packaging issued a recall for specific item(s) and lot(s) of Aligned Medical Solutions (AMS) convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lidocaine HCl injection USP due to supplier quality issues.

Windstone Medical Packaging issued a recall for specific item(s) and lot(s) of Aligned Medical Solutions (AMS) convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lidocaine HCl injection USP due to supplier quality issues.

Cardiovascular procedure kits contain manifolds, the subject of another recall, that may have particulate within the fluid path, which has the potential to be introduced into blood circulation and become lodged within blood vessels.

This recall is being reported retroactively. Power Platform firmware is missing specific drive inhibit logic. This issue may allow the chair to drive under restricted conditions, and may create an unstable condition in certain circumstances.

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

The clinical CT scan may not automatically trigger after the Bolus Tracking scan and may need to be triggered manually. Additional Bolus Tracking shots may occur. This may result in the clinical acquisition being inadequate for diagnosis, causing a potential for patient rescan and receiving additional radiation.

Windstone Medical Packaging issued a recall for specific item(s) and lot(s) of Aligned Medical Solutions (AMS) convenience kits containing Elevaris Lidocaine HCl injection USP. Elevaris Medical Devices Inc. recalled the Lidocaine HCl injection USP due to supplier quality issues.

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization.

The clinical CT scan may not automatically trigger after the Bolus Tracking scan and may need to be triggered manually. Additional Bolus Tracking shots may occur. This may result in the clinical acquisition being inadequate for diagnosis, causing a potential for patient rescan and receiving additional radiation.