FoodMar 5, 2025
Arizona Foods Group FOOD SERVICE - Mombo s Vanilla Soft Serve Ice Cream Mix recall — FDA F-0572-2025
Product may contain egg, an undeclared allergen.
Class IFDA: TerminatedArizona Foods Group, Inc.
Latest records
Latest recalls — page 256
The newest recall records with useful source details are listed here.
DrugMar 5, 2025
Wuxi Medical lnstrument Factory Co ViaMed Alcohol Prep Pads, For External Use Only, 70% recall — FDA D-0247-2025
Lack of assurance of sterility and cGMP deviations observed at the manufacturing site.
Class IIFDA: OngoingWuxi Medical lnstrument Factory Co., Ltd.
DrugMar 5, 2025
Turbare Manufacturing Avastin 1.25 mg/0.05 mL in 0.25 mL Syringe, For Intravitreal Injection recall — FDA D-0248-2025
Lack of Assurance of Sterility: due to a quality control process deviation
Class IIFDA: CompletedTurbare Manufacturing
DrugMar 5, 2025
Padagis US Estradiol Gel, 0.1%, 0.25 mg/g, 30 packets per carton recall — FDA D-0246-2025
Defective Container: Some packets may not be fully sealed, potentially allowing for loss of Ethanol from the product.
Class IIFDA: CompletedPadagis US LLC
VehicleFeb 28, 2025
Maverick control module (tcm/pcm/tecm) recall — NHTSA campaign 25V127000
Ford Motor Company (Ford) is recalling certain 2022 Maverick vehicles previously repaired incorrectly under recall number 24V-590. The body and power train control modules may fail to…
control module (tcm/pcm/tecm)Ford Motor Company
VehicleFeb 28, 2025
Maverick control unit/module recall — NHTSA campaign 25V124000
Ford Motor Company (Ford) is recalling certain 2022 Maverick vehicles previously repaired incorrectly under recall number 24V-730. Under certain circumstances, the Antilock Brake System…
control unit/moduleFord Motor Company
VehicleFeb 28, 2025
Maverick Hybrid instrument cluster/panel recall — NHTSA campaign 25V123000
Ford Motor Company (Ford) is recalling certain 2022-2023 Maverick Hybrid vehicles previously repaired incorrectly under recall number 24V-140. The instrument panel cluster may not properly…
instrument cluster/panelFord Motor Company
VehicleFeb 28, 2025
Ford control module (tcm/pcm/tecm) recall — NHTSA campaign 25V133000
Ford Motor Company (Ford) is recalling certain 2022-2024 Maverick, 2022 Escape, and 2021-2022 Lincoln Corsair vehicles previously repaired incorrectly under recall number 24V-330. The…
control module (tcm/pcm/tecm)Ford Motor Company
VehicleFeb 28, 2025
Ford integrated trailer brake control recall — NHTSA campaign 25V132000
Ford Motor Company (Ford) is recalling certain 2021-2022 F-150, 2022 Maverick, Expedition, Lincoln Navigator, F-250, F-350, F-450, and F-550 vehicles previously repaired incorrectly under…
integrated trailer brake controlFord Motor Company
Medical DeviceFeb 26, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Allura Xper FD10/10 recall — FDA Z-1143-2025
Possibility of the patient falling from the table related to the mattress used on the patient table.
Class IFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceFeb 26, 2025
Medline Convenience Kits for Various Procedures: 1) CLOVIS RESP/INTUB DRAWER 2, Model Number recall — FDA Z-1183-2025
Kits contain recalled components due to reports of reduced skin barrier wear time. This refers to a shorter duration that a skin barrier can effectively adhere to and protect the skin…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceFeb 26, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Azurion 5 M20; Catalog numbers: (1) 722228, (2) 722232 recall — FDA Z-1156-2025
Possibility of the patient falling from the table related to the mattress used on the patient table.
Class IFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceFeb 26, 2025
RayStation- Intended as a Radiation Therapy Treatment Planning System recall — FDA Z-1193-2025
Inconsistency in the use of Density uncertainty in the RayStation functions Robust optimization, Robust evaluation and Compute perturbed dose for proton and light ion treatment plans when a…
Class IIFDA: OngoingRAYSEARCH LABORATORIES AB
Medical DeviceFeb 26, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Allura Xper FD20/20 recall — FDA Z-1150-2025
Possibility of the patient falling from the table related to the mattress used on the patient table.
Class IFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceFeb 26, 2025
RayStation- Intended as a Radiation Therapy Treatment Planning System recall — FDA Z-1194-2025
Inconsistency in the use of Density uncertainty in the RayStation functions Robust optimization, Robust evaluation and Compute perturbed dose for proton and light ion treatment plans when a…
Class IIFDA: OngoingRAYSEARCH LABORATORIES AB
Medical DeviceFeb 26, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Cardio Vascular-Allura Centron recall — FDA Z-1161-2025
Possibility of the patient falling from the table related to the mattress used on the patient table.
Class IFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceFeb 26, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Allura Xper FD10C recall — FDA Z-1152-2025
Possibility of the patient falling from the table related to the mattress used on the patient table.
Class IFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceFeb 26, 2025
remel BLOOD AGAR MacCONKEY AGAR BIPLATE, REF R02049, QTY 100, for invitro diagnostic use recall — FDA Z-1200-2025
Product may contain surface and subsurface contamination of Listeria monocytogenes which is typically visible immediately upon removal from the packaging, appearing on the blood side of the…
Class IIFDA: OngoingRemel, Inc.
Medical DeviceFeb 26, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Allura Xper FD10 - Catalog numbers: (1) 722003, (2) recall — FDA Z-1142-2025
Possibility of the patient falling from the table related to the mattress used on the patient table.
Class IFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceFeb 26, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Allura Xper FD20/10 recall — FDA Z-1148-2025
Possibility of the patient falling from the table related to the mattress used on the patient table.
Class IFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceFeb 26, 2025
Physio-Control LIFEPAK 15 V4/Masimo Rainbow Sensors: Masimo RD rainbow Adt 8 SpCO, SpO2, and recall — FDA Z-1184-2025
Due to an error message that prevents users from utilizing carboxyhemoglobin saturation and methemoglobin saturation sensors on their monitor/defibrillator system.
Class IIFDA: OngoingPhysio-Control, Inc.
Medical DeviceFeb 26, 2025
Augustine Temperature Management Hot Dog PATIENT WARMING, Underbody Warming Mattress + recall — FDA Z-1199-2025
There is over-molding that stabilizes the connection between the cable and cable-entry on the mattress. It turns out that after about a year of use, the connector cable on the mattress can…
Class IIFDA: OngoingAugustine Temperature Management, LLC
Medical DeviceFeb 26, 2025
Dexcom G6, Continuous Glucose Monitoring System, REF: STK-OE-001 recall — FDA Z-1204-2025
Under very rare situations, the Dexcom G6 touchscreen receiver may not provide high or low glucose alarms/alerts as designed, which can result in two different conditions. First, if a…
Class IIFDA: OngoingDexcom, Inc.
Medical DeviceFeb 26, 2025
RayStation- Intended as a Radiation Therapy Treatment Planning System recall — FDA Z-1191-2025
Inconsistency in the use of Density uncertainty in the RayStation functions Robust optimization, Robust evaluation and Compute perturbed dose for proton and light ion treatment plans when a…
Class IIFDA: OngoingRAYSEARCH LABORATORIES AB
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Recent recall archives
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September 2026363 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categories