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.
Monthly breakdown
2024 recalls by month
Select a month to review the recall records reported during that period.
December 2024325 records · 4 categoriesNovember 2024355 records · 4 categoriesOctober 2024409 records · 4 categoriesSeptember 2024547 records · 4 categoriesAugust 2024327 records · 4 categoriesJuly 2024318 records · 4 categoriesJune 2024286 records · 4 categoriesMay 2024422 records · 4 categoriesApril 2024323 records · 4 categoriesMarch 2024332 records · 4 categoriesFebruary 2024425 records · 4 categoriesJanuary 2024298 records · 4 categories
2024 recalls — page 25
Records are ordered by the best available source date.
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)
Medical DeviceNov 6, 2024
KING LTSD,SIZE 2,W/SUCTION PORT STERILE-Inserted into a patient s pharynx through the mouth recall — FDA Z-0271-2025
Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because it introduces a new indication for pediatric use in an Oropharyngeal Airway.
Class IIFDA: OngoingKing Systems Corp. dba Ambu, Inc.
Medical DeviceNov 6, 2024
Olympus Corporation of the Americas Quest Spectrum 3 Fluorescent Imaging System recall — FDA Z-0232-2025
Does not meet the requirements for electromagnetic compatibility (EMC) of the standard IEC 60601-1-2. Electromagnetic interference occurring during a procedure may cause the device to…
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceNov 6, 2024
KING LTSD,SIZE 2.5, W/SUCTION PORT STERILE-Inserted into a patient s pharynx through the recall — FDA Z-0272-2025
Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because it introduces a new indication for pediatric use in an Oropharyngeal Airway.
Class IIFDA: OngoingKing Systems Corp. dba Ambu, Inc.
Medical DeviceNov 6, 2024
Integra LifeSciences SURG PAT XRAY 1X1 recall — FDA Z-0242-2025
Identified higher-than-expected levels of endotoxin within the raw material used to produce Codman Surgical Patties and Strips that may have resulted in out-of-specification levels of…
Class IIFDA: OngoingIntegra LifeSciences Corp.
Medical DeviceNov 6, 2024
Vial2Bag Advanced 20mm Admixture Device recall — FDA Z-0283-2025
Due to packaging damage from heat exposure during shipping/transportation that may result in a breach in the sterile barrier.
Class IIFDA: OngoingWest Pharmaceutical Services AZ, Inc.
Medical DeviceNov 6, 2024
Integra LifeSciences SURG STRP 1/4X6 recall — FDA Z-0249-2025
Identified higher-than-expected levels of endotoxin within the raw material used to produce Codman Surgical Patties and Strips that may have resulted in out-of-specification levels of…
Class IIFDA: OngoingIntegra LifeSciences Corp.
Medical DeviceNov 6, 2024
DATEX--OHMEDA GE Healthcare Giraffe Omnibed Carestation CS1, combination infant incubator recall — FDA Z-0140-2025
Prior to current established manufacturing practices, higher levels of airborne formaldehyde exposure from newly manufactured incubators could be seen during clinical use that would rapidly…
Class IFDA: CompletedDATEX--OHMEDA, Inc.
Medical DeviceNov 6, 2024
Integra LifeSciences SURG PAT XRAY 1/2X3 recall — FDA Z-0245-2025
Identified higher-than-expected levels of endotoxin within the raw material used to produce Codman Surgical Patties and Strips that may have resulted in out-of-specification levels of…
Class IIFDA: OngoingIntegra LifeSciences Corp.
Medical DeviceNov 6, 2024
Integra LifeSciences SURG PAT XRAY 1/4X1-1/2 recall — FDA Z-0236-2025
Identified higher-than-expected levels of endotoxin within the raw material used to produce Codman Surgical Patties and Strips that may have resulted in out-of-specification levels of…
Class IIFDA: OngoingIntegra LifeSciences Corp.
Medical DeviceNov 6, 2024
Integra LifeSciences MICR PATIE RND recall — FDA Z-0235-2025
Identified higher-than-expected levels of endotoxin within the raw material used to produce Codman Surgical Patties and Strips that may have resulted in out-of-specification levels of…
Class IIFDA: OngoingIntegra LifeSciences Corp.
Medical DeviceNov 6, 2024
KING LTSD,SIZE 0, W/SUCTION PORT NON-STERILE KIT-Inserted into a patient s pharynx through recall — FDA Z-0273-2025
Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because it introduces a new indication for pediatric use in an Oropharyngeal Airway.
Class IIFDA: OngoingKing Systems Corp. dba Ambu, Inc.
About the 2024 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.