FoodFeb 19, 2025
The Candy Basket Orange Jelly Sticks MILK, item number CB741-M, is packed and recall — FDA F-0555-2025
Undeclared Yellow #6, and Sodium Benzoate.
Class IIFDA: TerminatedThe Candy Basket Inc.
February 2025 recalls — page 6
These records include useful source details for the selected month.
FoodFeb 19, 2025
PIU CHE DOLCI Sweet Cream Mini Patisseries, 30 piece tray of mini pastries recall — FDA F-0551-2025
Due to potential Salmonella contamination
Class IFDA: TerminatedPIU CHE DOLCI Inc.
FoodFeb 19, 2025
Wismettac Asian Foods Front Panel: Shirakiku brand, CURVEE PUFFS CORN PUFF SNACK recall — FDA F-0549-2025
Undeclared allergen (Milk) in Shirakiku brand Curvee Puffs Corn Puff Snack
Class IFDA: TerminatedWismettac Asian Foods, Inc.
FoodFeb 19, 2025
The Candy Basket Marionberry Jelly Sticks MILK, item number CB745-M, is packed recall — FDA F-0559-2025
Undeclared Red #3, Blue #1, Potassium Sorbate, and Propylene Glycol.
Class IIIFDA: TerminatedThe Candy Basket Inc.
FoodFeb 19, 2025
The Candy Basket Lemon Jelly Sticks DARK, item number CB750-D, is packed and recall — FDA F-0557-2025
Undeclared Yellow #5 and Potassium Sorbate.
Class IIFDA: TerminatedThe Candy Basket Inc.
FoodFeb 19, 2025
The Candy Basket Lemon Jelly Sticks WHITE, item number CB750-W, is packed and recall — FDA F-0558-2025
Undeclared Yellow #5 and Potassium Sorbate.
Class IIFDA: TerminatedThe Candy Basket Inc.
FoodFeb 19, 2025
The Candy Basket Orange Jelly Sticks DARK, item number CB741-D, is packed and recall — FDA F-0556-2025
Undeclared Yellow #6, and Sodium Benzoate.
Class IIFDA: TerminatedThe Candy Basket Inc.
FoodFeb 19, 2025
AKT Trading Menma Ajitsuke prepared bamboo shoots recall — FDA F-0554-2025
CHOSHIYA branded MENMA AJITSUKE PREPARED BAMBOO SHOOTS missing "Keep Refrigerated" statement on package and are not shelf stable.
Class IFDA: TerminatedAKT Trading Inc.
FoodFeb 19, 2025
Wismettac Asian Foods Front Panel: Shirakiku brand, CURVEE PUFFS CORN PUFF SNACK recall — FDA F-0548-2025
Undeclared allergen (Milk) in Shirakiku brand Curvee Puffs Corn Puff Snack
Class IFDA: TerminatedWismettac Asian Foods, Inc.
FoodFeb 19, 2025
The Candy Basket Marionberry Jelly Sticks DARK, item number CB745-D, is packed recall — FDA F-0560-2025
Undeclared Red #3, Blue #1, Potassium Sorbate, and Propylene Glycol.
Class IIIFDA: TerminatedThe Candy Basket Inc.
FoodFeb 19, 2025
Riverside Natural Foods 1 recall — FDA F-0543-2025
may contain metal pieces
Class IIFDA: CompletedRiverside Natural Foods, Ltd.
VehicleFeb 17, 2025
Kia hard parts internal/mechanical recall — NHTSA campaign 25V099000
Kia America, Inc. (Kia) is recalling certain 2021-2023 Seltos and Soul vehicles. The piston oil rings may have been manufactured incorrectly, which can result in engine damage.
hard parts internal/mechanicalKia America, Inc.
VehicleFeb 14, 2025
Maverick tail lights recall — NHTSA campaign 25V095000
Ford Motor Company (Ford) is recalling certain 2022-2024 Maverick vehicles previously repaired incorrectly under recall number 24V-293. The body control module (BCM) may inadvertently…
tail lightsFord Motor Company
VehicleFeb 14, 2025
Maverick turn signal recall — NHTSA campaign 25V094000
Ford Motor Company (Ford) is recalling certain 2022-2024 Maverick vehicles previously repaired incorrectly under recall number 23V-848. In the event that one of the rear turn signals stops…
turn signalFord Motor Company
VehicleFeb 14, 2025
Ford Mustang electric power assist system recall — NHTSA campaign 25V096000
Ford Motor Company (Ford) is recalling certain 2022-2023 Ford Mustang vehicles previously repaired incorrectly under recall number 24V-493. The secondary steering torque sensor may not be…
electric power assist systemFord Motor Company
VehicleFeb 14, 2025
Ford seat belts recall — NHTSA campaign 25V093000
Ford Motor Company (Ford) is recalling certain 2020-2021 Explorer and Aviator vehicles. The seat belt buckle anchor bolts at one or more seating positions may be improperly secured.…
seat beltsFord Motor Company
VehicleFeb 14, 2025
Tesla electric power assist system recall — NHTSA campaign 25V092000
Tesla, Inc. (Tesla) is recalling certain 2023 Model 3 and Model Y vehicles operating software prior to 2023.38.4. The printed circuit board for the electronic power steering assist may…
electric power assist systemTesla, Inc.
VehicleFeb 13, 2025
Chrysler video (touch)screen/monitor/unit recall — NHTSA campaign 25V083000
Chrysler (FCA US, LLC) is recalling certain 2022 Jeep Grand Cherokee and 2021-2022 Jeep Grand Cherokee L vehicles. The center stack upper display (DCSD) contains a transistor that may…
video (touch)screen/monitor/unitChrysler (FCA US, LLC)
Medical DeviceFeb 12, 2025
Sysmex PS-10 Sample Preparation System with software version 1.5 and 1.6., Catalog Number recall — FDA Z-1113-2025
Sysmex was made aware of a report of false results due to carry-over caused by the sporadic omission of the probe wash step during antibody pipetting on the PS-10 Sample Preparation System.
Class IIFDA: OngoingSysmex America, Inc.
Medical DeviceFeb 12, 2025
Physio-Control LIFEPAK 35 ECG cable REF 11111-000041 recall — FDA Z-1102-2025
Product shipped with incorrect IFU. IFU does not include proper cleaning/disinfection instructions
Class IIFDA: OngoingPhysio-Control, Inc.
Medical DeviceFeb 12, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Allura Xper FD10C System Code: (1) 722001 recall — FDA Z-1079-2025
Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceFeb 12, 2025
Ethicon PERMA-HAND Silk Suture, REF: K872H, W723H, 623H, K833H recall — FDA Z-1097-2025
Sutures may have an open seal on the primary packaging, due to a manufacturing issue on a specific machine, and if issue is undetected could lead to breach in sterility, could introduce…
Class IIFDA: OngoingEthicon, LLC
Medical DeviceFeb 12, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V AlluraXper FD20 Biplane OR Table System Code: (1) recall — FDA Z-1082-2025
Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceFeb 12, 2025
Philips IntelliBridge EC10 Module recall — FDA Z-1106-2025
Potential failure to alarm for "No Device Data" INOP. The device to alarm after a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board.
Class IIFDA: OngoingPhilips North America 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.