FoodOct 30, 2024
Youngstown Grape Distributors Farmers Juice Watermelon Hydration packaged in a 12 fl recall — FDA F-0062-2025
Incomplete pasteurization
Class IIFDA: TerminatedYoungstown Grape Distributors, 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 33
Records are ordered by the best available source date.
FoodOct 30, 2024
Choi's Kimchi packaged 16oz plastic pouch with spout, keep refrigerated recall — FDA F-0055-2025
Salmonella.
Class IFDA: TerminatedChoi's Kimchi LLC
FoodOct 30, 2024
Youngstown Grape Distributors Farmers Juice Focus Greens packaged in a 12 fl recall — FDA F-0060-2025
Incomplete pasteurization
Class IIFDA: TerminatedYoungstown Grape Distributors, Inc.
FoodOct 30, 2024
Youngstown Grape Distributors Happy Moose Juice Tropical Roots packaged in a plastic 12 fl recall — FDA F-0058-2025
Incomplete pasteurization
Class IIFDA: TerminatedYoungstown Grape Distributors, Inc.
FoodOct 30, 2024
Salt City Baking Company Sour Charlie bread, #2092, bag of 6 rolls recall — FDA F-0057-2025
Undeclared Wheat flour. Product contains wheat flour but product was sold without the Ingredients Statement.
Class IIFDA: TerminatedSalt City Baking Company, LLC
FoodOct 30, 2024
Horizon Organic Dairy refrigerated, One Pint recall — FDA F-0064-2025
Potential for premature product spoilage during shelf life.
Class IIFDA: TerminatedHorizon Organic Dairy, LLC
FoodOct 30, 2024
Youngstown Grape Distributors Farmers Juice Carrot Digest packaged in a 12 fl recall — FDA F-0061-2025
Incomplete pasteurization
Class IIFDA: TerminatedYoungstown Grape Distributors, Inc.
FoodOct 30, 2024
HP Hood Lactaid Lactose Reduced milk 1 recall — FDA F-0054-2025
Milk may contain undeclared almond from almond milk
Class IFDA: TerminatedHP Hood LLC
FoodOct 30, 2024
Best Express Foods Principal Display: SureLife Foods PALEO BARS, Net Wt recall — FDA F-0063-2025
Potential undeclared gluten product is labeled as gluten free but consumer advocacy group testing revealed results above 20ppm for gluten.
Class IIFDA: OngoingBest Express Foods, Inc.
FoodOct 30, 2024
Youngstown Grape Distributors Happy Moose Juice Strawberry Field packaged in a plastic 12 fl recall — FDA F-0059-2025
Incomplete pasteurization
Class IIFDA: TerminatedYoungstown Grape Distributors, Inc.
VehicleOct 25, 2024
Mustang instrument cluster/panel recall — NHTSA campaign 24V802000
Ford Motor Company (Ford) is recalling certain 2024 Mustang vehicles. The Instrument Panel Cluster (IPC) may not illuminate at startup or while driving. As such, these vehicles fail to…
instrument cluster/panelFord Motor Company
VehicleOct 25, 2024
Ford back over prevention software recall — NHTSA campaign 24V801000
Ford Motor Company (Ford) is recalling certain 2025 Explorer and Lincoln Aviator vehicles. The rearview camera image may fail when the vehicle speed reaches 10 MPH or greater. As such,…
back over prevention softwareFord Motor Company
VehicleOct 24, 2024
General Motors control module software recall — NHTSA campaign 24V797000
General Motors, LLC (GM) is recalling certain 2020-2022 Chevrolet Silverado 1500, 2500, 3500, GMC Sierra 1500, 2500, 3500, 2021 Cadillac Escalade, Escalade ESV, Chevrolet Tahoe, Suburban,…
control module softwareGeneral Motors, LLC
VehicleOct 24, 2024
Ram 1500 hub recall — NHTSA campaign 24V794000
Chrysler (FCA US, LLC) is recalling certain 2025 Ram 1500 vehicles. The front wheel hub encoder rings may be damaged, which can disable the electronic stability control system. As such,…
hubChrysler (FCA US, LLC)
Medical DeviceOct 23, 2024
Stryker 1.2mm Cross Cut Fissure - Intended for use in the cutting, drilling, reaming recall — FDA Z-0063-2025
May exhibit endotoxin levels greater than 2.15 EU/device, fever and inflammation may occur from endotoxin exposure and meningitis may only occur if there is contact with cerebrospinal fluid…
Class IIFDA: OngoingStryker Corporation
Medical DeviceOct 23, 2024
Boston Scientific AVVIGO+ Multi-Modality Guidance System, AVVIGO II TO AVVIGO MOB UPGRADE US recall — FDA Z-0116-2025
Boston Scientific has received reports indicating the grid mark overlay on the cross-sectional view did not present correctly when an OptiCross 18 Peripheral Imaging Catheter was connected…
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceOct 23, 2024
Merit Medical Systems Monarch Inflation Device MAP 112 Access-9 Large Bore Hemostasis Value recall — FDA Z-0058-2025
Due to a manufacturing process resulting in holes/breaches in the Tyvek sterile barrier.
Class IIFDA: OngoingMerit Medical Systems, Inc.
Medical DeviceOct 23, 2024
DATEX--OHMEDA GE Heathcare Giraffe OmniBed Carestation, Model Number 2082844-001-XXX recall — FDA Z-0048-2025
GE HealthCare has become aware that for certain Giraffe OmniBed and Giraffe OmniBed Carestation devices, the screw that secures the doors that cover the warmer heaters may not have been…
Class IFDA: OngoingDATEX--OHMEDA, Inc.
Medical DeviceOct 23, 2024
Medtronic Neuromodulation Vanta Implantable Neurostimulator (INS), Model 977006 recall — FDA Z-0132-2025
Model 977006 Vanta INS batterty life has depleted faster than HCPs or patients expected leading to outpatient reprogramming or earlier than anticipated surgical replacements.
Class IIFDA: OngoingMedtronic Neuromodulation
Medical DeviceOct 23, 2024
MEDLINE OPEN HEART NIMC KIT, REF DYNJ908840 recall — FDA Z-0124-2025
Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceOct 23, 2024
Boston Scientific AVVIGO+ Multi-Modality Guidance System, AVVIGO + MOB SYSTEM - ZERO COST US recall — FDA Z-0103-2025
Boston Scientific has received reports indicating the grid mark overlay on the cross-sectional view did not present correctly when an OptiCross 18 Peripheral Imaging Catheter was connected…
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceOct 23, 2024
Wilson-Cook Medical Cook Medical Hemo-7 Hemospray Endoscopic Hemostat, REF G56572, 2.8 mm recall — FDA Z-0036-2025
Specific lots of product have been manufactured with nonconforming raw materials.
Class IIFDA: OngoingWilson-Cook Medical Inc.
Medical DeviceOct 23, 2024
Boston Scientific AVVIGO+ Multi-Modality Guidance System, AVVIGO II TO AVVIGO MOB UPGRADE recall — FDA Z-0115-2025
Boston Scientific has received reports indicating the grid mark overlay on the cross-sectional view did not present correctly when an OptiCross 18 Peripheral Imaging Catheter was connected…
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceOct 23, 2024
CHANGE HEALTHCARE CANADA COMPANY McKesson Cardiology Hemo recall — FDA Z-0128-2025
A potential issue has been identified in Change Healthcare Cardiology Hemo where incorrect data entry can lead to inaccurate hemodynamic calculations, potentially resulting in misdiagnosis…
Class IIFDA: OngoingCHANGE HEALTHCARE CANADA COMPANY
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.