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All product recalls affecting Mississippi.
Includes nationwide recalls (tagged “Nationwide”) and recalls with Mississippi in the distribution area.
This recall involves TEMI Toys Go Basketball children's toys. The recalled toy has five multicolored levels and a basketball hoop with a character's face at the top. The toy measures about 13 inches high by 4 inches wide and comes with three yellow balls. "TEMI GO BASKETBALL" is printed on the front of the product packaging.
This recall involves Altafit af28 smartwatches. The recalled smartwatch was sold in gold and silver tones and has a 1.68-inch color touchscreen and two bands, one bejeweled and one mesh. It came in a golden case with a wireless charging pad and cable. "ALTAFIT FCC ID 2BHG8-AF28" is on the back of the watch.
This recall involves Pet Zone-branded Laser Pointer & LED Ball pet toys, sold with six preinstalled button cell batteries. The laser pointer is white with blue paw prints and measures about 2.9 inches long. "Danger" and "Accession No. 2430278-000" are printed on a silver label located on the laser pointer tube. The motion-activated LED ball is clear and measures about 1.6 inches in diameter. The "PET ZONE" logo and "LASER POINTER & LED BALL" are printed on the front of the product packaging and "Item #:15712EAM" on the back.
This recall involves Séfralls Hair Generation Serum. The hair serum comes in an amber dropper bottle with a white and gold dropper and a white, black and gold label. "Séfralls" and "Minoxidil" are printed on the label located on the front of the bottle.
CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity above the current Acceptable Intake Level.
CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity above the current Acceptable Intake Level.
CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity above the current Acceptable Intake Level.
Certain CADD 50 mL and 100 mL Medication Cassette Reservoirs may exhibit weakened medication bag welds along the bag perimeter inside the plastic housing. This could result in medication leakage along the bag perimeter.
International Motors, LLC (International) is recalling certain 2016-2024 IC Bus CESB school buses. The brake pressure switch assembly may leak brake fluid into the brake pressure switch's electrical components and cause an electrical short-circuit.
Potential for undetected, deformed a-traumatic tips.
Certain CADD 50 mL and 100 mL Medication Cassette Reservoirs may exhibit weakened medication bag welds along the bag perimeter inside the plastic housing. This could result in medication leakage along the bag perimeter.
As a result of Post-Market half-time stability testing, false negative test result was observed for a positive sample type.
International Motors, LLC (International) is recalling certain 2018 International 4000 Series 4300, 2017-2025 MV, 2018-2024 1300 FBC, 2018-2025 IC Bus TC, and 2024-2025 IC Bus CECB vehicles. The brake pressure switch assembly may leak brake fluid into the brake pressure switch's electrical components and cause an electrical short-circuit.
Reports of out-of-box failures discovered during the limited launch phase. Failure modes included angled deformity at the attachment site of the Harvesting Tool Jaws and the distal end of the Harvesting Tool Shaft, jaws not fully closed out of box, and heater wire lifted/flexed away from jaws.
Fontaine Modification Company (Fontaine Modification) is recalling certain 2022-2024 Freightliner Business Class M2 vehicles. Welds may crack and fail, allowing the Intermediate steering shaft assembly to detach from the steering column.
The catheters may not retain their shape.
Unapproved Drug Claims and Misbranded.
CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity observed to be above the FDA-recommended limit of NMT 4.0 ppm
Unapproved Drug Claims.
Unapproved Drug Claims.