FoodFeb 4, 2026
Prima Vera Nueva Butternut Squash Tamales with Roasted Green Chiles, NO DAIRY recall — FDA H-0430-2026
Potential contamination with biological hazards (Listeria monocytogenes).
Class IIFDA: TerminatedPrima Vera Nueva, Inc.
Monthly breakdown
2026 recalls by month
Select a month to review the recall records reported during that period.
September 2026300 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 categories
2026 recalls — page 110
Records are ordered by the best available source date.
FoodFeb 4, 2026
Weaver's Brew Goldenroot Lemon Ginger Jalapeno Ginger Beer recall — FDA H-0438-2026
Ginger Beer products might contain ginger juice that did not undergo the required pasteurization process.
Class IIFDA: TerminatedWeaver's Brew LLC
FoodFeb 4, 2026
Prima Vera Nueva Roasted Green Chile & Jack Cheese Tamales Ingredients: Organic recall — FDA H-0432-2026
Potential contamination with biological hazards (Listeria monocytogenes).
Class IIFDA: TerminatedPrima Vera Nueva, Inc.
FoodFeb 4, 2026
Prima Vera Nueva Mushroom, Spinach & Salsa Tamales with 2 Cheeses Ingredients recall — FDA H-0424-2026
Potential contamination with biological hazards (Listeria monocytogenes).
Class IIFDA: TerminatedPrima Vera Nueva, Inc.
FoodFeb 4, 2026
BHARAT BAZAR SOMA KITCHEN NATURAL ASAFOETIDA Net Wt recall — FDA H-0417-2026
Undeclared wheat.
Class IIFDA: OngoingBHARAT BAZAR
DrugFeb 4, 2026
methylprednisolone tablets, USP Dosepak, 4 mg, 1 Blister Card per Carton containing 21 recall — FDA D-0299-2026
Labeling: Not Elsewhere Classified. Incorrect orientation of the blister foil applied to the blister cavities, which results in incorrect dosing information when following the directions on…
Class IIFDA: OngoingGreenstone Llc
DrugFeb 4, 2026
parodontax (cetylpyridinium chloride)ACTIVE GUM HEALTH, Mouthwash, Mint recall — FDA D-0297-2026
Labeling: Incorrect or Missing Lot and/or Exp Date: Potential for missing or illegible lot and expiration date coding on the bottles.
Class IIIFDA: OngoingHaleon US Holdings LLC
VehicleFeb 2, 2026
Chrysler brake lights recall — NHTSA campaign 26V059000
Chrysler (FCA US, LLC) is recalling certain 2024-2026 Jeep Wagoneer S, 2025-2026 Ram 1500 Pickup, Ram 2500 Pickup, Ram 3500 Pickup, Ram 3500 Cab Chassis, Ram 4500 Cab Chassis, Ram 5500 Cab…
brake lightsChrysler (FCA US, LLC)
VehicleJan 30, 2026
BMW starter motor recall — NHTSA campaign 26V056000
BMW of North America, LLC (BMW) is recalling certain 2021-2023 Toyota Supra, 2022-2023 2 Series Coupe, 2021-2024 5 Series (xDrive), 2021-2022 Z4, 2022-2024 4 Series (Gran Coupe), 2021-2024…
starter motorBMW of North America, LLC
VehicleJan 29, 2026
Honda critical fasteners recall — NHTSA campaign 26V054000
Honda (American Honda Motor Co.) is recalling certain 2023 Honda Accord, Accord Hybrid, and 2024 HR-V, Pilot, and Acura Integra vehicles. The driver's seat cushion frame may not have been…
critical fastenersHonda (American Honda Motor Co.)
VehicleJan 29, 2026
Chrysler coil springs recall — NHTSA campaign 26V051000
Chrysler (FCA US, LLC) is recalling certain 2021-2023 Jeep Grand Cherokee L and 2022-2023 Jeep Grand Cherokee vehicles. The rear coil springs may be incorrectly installed and detach from…
coil springsChrysler (FCA US, LLC)
Medical DeviceJan 28, 2026
GVS TM SQ40S Blood Transfusion Filter recall — FDA Z-1157-2026
Due to products being released for distribution prior to completion of the required quality control release process the sterility assurance cannot be confirmed.
Class IIFDA: OngoingGVS TM, Inc.
Medical DeviceJan 28, 2026
EDAN Patient Monitor recall — FDA Z-1147-2026
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
Class IIFDA: OngoingEdan Diagnostics
Medical DeviceJan 28, 2026
MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed, REF MDR107002E recall — FDA Z-1011-2026
Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating the bed above its specified…
Class IFDA: OngoingMedline Industries, LP
Medical DeviceJan 28, 2026
EDAN Patient Monitor recall — FDA Z-1145-2026
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
Class IIFDA: OngoingEdan Diagnostics
Medical DeviceJan 28, 2026
Community Products Rifton Equipment, Low Base TRAM recall — FDA Z-1138-2026
Potential for fraying on the body support strap.
Class IIFDA: OngoingCommunity Products, LLC
Medical DeviceJan 28, 2026
EDAN Fetal & Maternal Monitor recall — FDA Z-1141-2026
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
Class IIFDA: OngoingEdan Diagnostics
Medical DeviceJan 28, 2026
RAYSEARCH LABORATORIES AB RayStation/RayPlan recall — FDA Z-1102-2026
Potential for the invalidation for calculated radiation dose does not work as intended for certain Regions of Interest (ROIs). This issue occurs for some ROI(s) which have no contours and…
Class IIFDA: OngoingRAYSEARCH LABORATORIES AB
Medical DeviceJan 28, 2026
Ion Endoluminal System Ion Vision Probe Bag recall — FDA Z-1134-2026
Due to probe bags that may have a compromised or incomplete sterile pouch seal.
Class IIFDA: OngoingIntuitive Surgical, Inc.
Medical DeviceJan 28, 2026
Beckman Coulter Ireland The LDL-Cholesterol assay is comprised of two distinct phases recall — FDA Z-1135-2026
Beckman Coulter identified that LDL Cholesterol OSR6x96 is not meeting the performance claim listed in the Instructions for Use (IFU). LDL Cholesterol reagent showed clinically significant…
Class IIFDA: OngoingBeckman Coulter Ireland, Inc.
Medical DeviceJan 28, 2026
Mazor X robotic guidance system REF: TPL0059 recall — FDA Z-1122-2026
Software errors that can result in incorrect surgical instrument positioning during spinal surgery.
Class IIFDA: OngoingMazor Robotics Ltd
Medical DeviceJan 28, 2026
VOLT" Wrist Treatment System 2.4/2.7 2Column Dist Radius Plate 6Hd/10Shaft/Left/Std/139mm recall — FDA Z-1131-2026
The supplier manufactured anatomical left plates with an incorrect thread orientation.
Class IIFDA: OngoingTyber Medical
Medical DeviceJan 28, 2026
EDAN Patient Monitor recall — FDA Z-1148-2026
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
Class IIFDA: OngoingEdan Diagnostics
Medical DeviceJan 28, 2026
Philips Patient Information Center iX recall — FDA Z-1156-2026
A recent software (SW) patch modifies Mobile Event Notification filter settings without providing any indication to the user when upgrading the system.
Class IIFDA: OngoingPhilips North America
About the 2026 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.