DrugMay 28, 2025
KENIL HEALTHCARE PRIVATE Nature Mint Anticavity Fluoride Toothpaste, Sodium recall — FDA D-0439-2025
CGMP Deviations
Class IIFDA: TerminatedKENIL HEALTHCARE PRIVATE LIMITED
Monthly breakdown
2025 recalls by month
Select a month to review the recall records reported during that period.
December 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categoriesSeptember 2025285 records · 4 categoriesAugust 2025239 records · 4 categoriesJuly 2025370 records · 4 categoriesJune 2025342 records · 4 categoriesMay 2025258 records · 4 categoriesApril 2025302 records · 4 categoriesMarch 2025259 records · 4 categoriesFebruary 2025260 records · 4 categoriesJanuary 2025354 records · 4 categories
2025 recalls — page 104
Records are ordered by the best available source date.
DrugMay 28, 2025
Airsupra (albuterol and budesonide) inhalation aerosol, 90 mcg/80 mcg per inhalation recall — FDA D-0444-2025
Defective delivery system
Class IIFDA: OngoingAsttraZeneca Pharmaceuticals LP
DrugMay 28, 2025
KENIL HEALTHCARE PRIVATE Nature Mint Anticavity Fluoride Toothpaste, Sodium recall — FDA D-0438-2025
CGMP Deviations
Class IIFDA: TerminatedKENIL HEALTHCARE PRIVATE LIMITED
VehicleMay 23, 2025
Ford engine recall — NHTSA campaign 25V345000
Ford Motor Company (Ford) is recalling certain 2020-2023 Escape, 2021-2023 Corsair, and 2022-2023 Maverick vehicles equipped with 2.5L HEV or PHEV engines that were repaired incorrectly…
engineFord Motor Company
VehicleMay 23, 2025
Ford electrical system recall — NHTSA campaign 25V343000
Ford Motor Company (Ford) is recalling certain 2024-2025 Lincoln Nautilus, 2023-2025 Escape, 2023 Lincoln Corsair, 2025 Lincoln Corsair, Maverick, and Bronco Sport vehicles equipped with a…
electrical systemFord Motor Company
VehicleMay 23, 2025
F-150 back up lights recall — NHTSA campaign 25V348000
Ford Motor Company (Ford) is recalling certain 2021 F-150 vehicles equipped with the Onboard Scales feature that were repaired incorrectly under recall 24V443. An over-the-air software…
back up lightsFord Motor Company
Medical DeviceMay 21, 2025
LeMaitre Vascular Pruitt Irrigation Occlusion Catheter recall — FDA Z-1752-2025
During internal product testing, it was observed that some packages to have incomplete seals (sterile barrier).
Class IIFDA: OngoingLeMaitre Vascular, Inc.
Medical DeviceMay 21, 2025
AirLife Infant Heated Wire Circuit recall — FDA Z-1698-2025
Adapters may disconnect during setup or while in use, potentially interrupting ventilation. Any disconnection can result in severe consequences for neonates, including hypoxia, hypercapnia,…
Class IFDA: OngoingVyaire Medical
Medical DeviceMay 21, 2025
Klinika Mdical Gmb KliniTray. KlinioTray. Tissue resection margin examination board/small recall — FDA Z-1768-2025
Potential for microbial contamination.
Class IIFDA: OngoingKlinika Mdical Gmb
Medical DeviceMay 21, 2025
Augmedics Perc Pin Adaptor, Model/Catalog Number AMCH07200, a component of the xvision Spine recall — FDA Z-1761-2025
The perc pin adaptor AMCH07200 tightening knob was found to be inconvenient to the user and the tightening markings found to be improperly placed.
Class IIFDA: OngoingAugmedics Ltd.
Medical DeviceMay 21, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Intera CV recall — FDA Z-1781-2025
The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceMay 21, 2025
Nipro Renal Soultions USA MedicaLyte Liquid Bicarbonate Concentrate recall — FDA Z-1730-2025
Potential for the presence of visible foreign matter.
Class IFDA: OngoingNipro Renal Soultions USA, Corporation
Medical DeviceMay 21, 2025
LeMaitre Vascular TufTex Over-the-Wire Embolectomy Catheter recall — FDA Z-1750-2025
During internal product testing, it was observed that some packages to have incomplete seals (sterile barrier).
Class IIFDA: OngoingLeMaitre Vascular, Inc.
Medical DeviceMay 21, 2025
LeMaitre Vascular Pruitt Occlusion Catheter recall — FDA Z-1751-2025
During internal product testing, it was observed that some packages to have incomplete seals (sterile barrier).
Class IIFDA: OngoingLeMaitre Vascular, Inc.
Medical DeviceMay 21, 2025
AVID Medical Halyard SUTURE PACK CABG recall — FDA Z-1742-2025
An issue with a raw material used to coat some surgical needles that may result in diminished performance and/or removal of some silicone needle coating during use.
Class IIFDA: OngoingAVID Medical, Inc.
Medical DeviceMay 21, 2025
Contour Gold Eyelid Weight recall — FDA Z-1744-2025
Due to mislabeling of products
Class IIFDA: OngoingMeddev Corp
Medical DeviceMay 21, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Intera 1.0T Power/Pulsar recall — FDA Z-1773-2025
The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceMay 21, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Intera 1.5T, Model Numbers: 781195 and 781295 recall — FDA Z-1774-2025
The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceMay 21, 2025
ICU Medical LifeShield Drug Library Management (DLM), LifeShield Infusion Safety Software recall — FDA Z-1763-2025
Firm has identified Drug Library Management defects in the software: 1) DLM software does not allow user to create percentage dose rate or rate change values with certain limits,…
Class IIFDA: OngoingICU Medical, Inc.
Medical DeviceMay 21, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Intera 1.5T R11 recall — FDA Z-1779-2025
The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceMay 21, 2025
Medical Depot iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Oxygen Concentrator recall — FDA Z-1727-2025
Potential for DC Power Supply housing to become hot to the touch and deform the plastic housing.
Class IFDA: OngoingMedical Depot Inc.
Medical DeviceMay 21, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Intera 1.5T Power/Pulsar recall — FDA Z-1778-2025
The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceMay 21, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Intera 3.0T Quasar Dual recall — FDA Z-1780-2025
The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceMay 21, 2025
Contour Gold Eyelid Weight recall — FDA Z-1745-2025
Due to mislabeling of products
Class IIFDA: OngoingMeddev Corp
About the 2025 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.