FoodNov 13, 2024
My Chai MySyrup Sugar Free Raspberry Syrup recall — FDA F-0117-2025
Acidified product is recalled due to lack production record.
Class IIIFDA: TerminatedMy Chai Inc.
November 2024 recalls — page 11
These records include useful source details for the selected month.
FoodNov 13, 2024
Perfection Bakeries Aunt Millie s Bakehouse Whole Grain White Hot Dog Buns 6" recall — FDA F-0104-2025
Undeclared sesame
Class IFDA: TerminatedPerfection Bakeries LLC
FoodNov 13, 2024
My Chai 68 fl recall — FDA F-0107-2025
Acidified Chai Tea products are recalled because pH was found above 4.1 and lack production record.
Class IIFDA: TerminatedMy Chai Inc.
FoodNov 13, 2024
My Chai MySyrup Sugar Free Almond Syrup recall — FDA F-0111-2025
Acidified product is recalled due to lack production record.
Class IIIFDA: TerminatedMy Chai Inc.
FoodNov 13, 2024
My Chai MySyrup Sugar Free Peppermint Syrup recall — FDA F-0116-2025
Acidified product is recalled due to lack production record.
Class IIIFDA: TerminatedMy Chai Inc.
FoodNov 13, 2024
My Chai MyChai Chai Tea Concentrate Original Double recall — FDA F-0110-2025
Acidified Chai Tea product is recalled due to lack production record.
Class IIIFDA: TerminatedMy Chai Inc.
FoodNov 13, 2024
Perfection Bakeries Aunt Millie s Bakehouse 100% Whole Wheat Pullman Bread 1/2" recall — FDA F-0101-2025
Undeclared sesame
Class IFDA: TerminatedPerfection Bakeries LLC
FoodNov 13, 2024
My Chai MyChai Chai Tea Concentrate Original recall — FDA F-0106-2025
Acidified Chai Tea products are recalled because pH was found above 4.1 and lack production record.
Class IIFDA: TerminatedMy Chai Inc.
FoodNov 13, 2024
EM Tortillas Bulk Mexican sweet bread including conchas, fino ellotes, fino recall — FDA F-0097-2025
Undeclared allergens; wheat, soy, and eggs.
Class IIFDA: TerminatedEM Tortillas, LLC
FoodNov 13, 2024
My Chai MyChai Chai Tea Concentrate Super recall — FDA F-0109-2025
Acidified Chai Tea product is recalled due to lack production record.
Class IIIFDA: TerminatedMy Chai Inc.
FoodNov 13, 2024
My Chai MySyrup Sugar Free Madagascar Vanilla Syrup recall — FDA F-0115-2025
Acidified product is recalled due to lack production record.
Class IIIFDA: TerminatedMy Chai Inc.
FoodNov 13, 2024
My Chai MySyrup Sugar Free Caramel Syrup recall — FDA F-0112-2025
Acidified product is recalled due to lack production record.
Class IIIFDA: TerminatedMy Chai Inc.
FoodNov 13, 2024
Perfection Bakeries Aunt Millie s Bakehouse White Pullman Bread 1/2" Sliced 22 recall — FDA F-0100-2025
Undeclared sesame
Class IFDA: TerminatedPerfection Bakeries LLC
FoodNov 13, 2024
My Chai MySyrup Sugar Free Salted Caramel Syrup recall — FDA F-0118-2025
Acidified product is recalled due to lack production record.
Class IIIFDA: TerminatedMy Chai Inc.
FoodNov 13, 2024
My Chai Oregon Orchards Banana Smoothie Mix recall — FDA F-0119-2025
Acidified product is recalled due to lack production record.
Class IIIFDA: TerminatedMy Chai Inc.
DrugNov 13, 2024
MAXIMUM STRENGTH COUGH AND CHEST CONGESTION AND NIGHTTIME SEVERE COLD AND FLU COMBO PACK recall — FDA D-0034-2025
Crystallization: Lack of uniformity - a change in texture, chunky, grainy, and small crystal substances inside the bottles.
Class IIIFDA: OngoingDenison Pharmaceuticals, LLC
DrugNov 13, 2024
MAXIMUM STRENGTH COUGH AND CHEST CONGESTION AND NIGHTTIME SEVERE COLD AND FLU COMBO PACK recall — FDA D-0033-2025
Crystallization: Lack of uniformity - a change in texture, chunky, grainy, and small crystal substances inside the bottles.
Class IIIFDA: OngoingDenison Pharmaceuticals, LLC
DrugNov 13, 2024
Direct Rx Ibuprofen 800mg, Generic for: Motrin, Each tablet contains: Ibuprofen, USP 800 mg recall — FDA D-0041-2025
Failed Impurities/Degradation Specifications: Product failed impurity specifications at the 18-month stability testing.
Class IIFDA: OngoingDirect Rx
DrugNov 13, 2024
Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 5mL bottles recall — FDA D-0035-2025
Defective Container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle
Class IIFDA: OngoingFDC Limited
VehicleNov 12, 2024
X3 30 xDrive curtain recall — NHTSA campaign 24V856000
BMW of North America, LLC (BMW) is recalling certain 2025 X3 30 xDrive vehicles. The gas generator in the right-side head curtain air bag may have been assembled incorrectly.
curtainBMW of North America, LLC
VehicleNov 8, 2024
Escape instrument cluster/panel recall — NHTSA campaign 24V850000
Ford Motor Company (Ford) is recalling certain 2024-2025 Escape vehicles. The passenger side instrument panel cover may have been manufactured incorrectly, which can cause the air bag not…
instrument cluster/panelFord Motor Company
VehicleNov 8, 2024
Ford labels recall — NHTSA campaign 24V852000
Ford Motor Company (Ford) is recalling certain 2020-2025 Explorer, Lincoln Aviator, 2020-2024 Escape, Lincoln Corsair, 2018-2024 F-150, Expedition and Lincoln Navigator vehicles. The air…
labelsFord Motor Company
VehicleNov 7, 2024
Hyundai Motor switches/knobs/buttons recall — NHTSA campaign 24V843000
Hyundai Motor America (Hyundai) is recalling certain 2024 Santa Fe and Santa Fe Hybrid vehicles. The overhead console rear sunshade switch knob may not be fully recessed, which can result…
switches/knobs/buttonsHyundai Motor America
VehicleNov 7, 2024
Chrysler control unit/module recall — NHTSA campaign 24V838000
Chrysler (FCA US, LLC) is recalling certain 2018-2019 Jeep Grand Cherokee and Dodge Durango vehicles. A malfunction in the antilock-brake system (ABS) module may incorrectly illuminate the…
control unit/moduleChrysler (FCA US, LLC)
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.