FoodFeb 18, 2026
Lee's Commissary Brand: Red Button Movie House Popcorn Pack Size: 24 oz recall — FDA H-0496-2026
Product may contain foreign material.
Class IIFDA: TerminatedLee's Commissary
Latest records
Latest recalls — page 81
The newest recall records with useful source details are listed here.
FoodFeb 18, 2026
McCain Foods USA Sonic Tots, item number SON00543 recall — FDA H-0493-2026
Foreign material (small hard plastic fragments).
Class IIFDA: TerminatedMcCain Foods USA Inc
FoodFeb 18, 2026
Karison brand BESAN LADDOO recall — FDA H-0505-2026
Product contains milk, which is undeclared in the ingredient statement.
Class IIFDA: TerminatedKarison Foods & Snacks, Inc.
FoodFeb 18, 2026
Ventura Foods CREAMY PEANUT BUTTER NET WT 1.12 OZ recall — FDA H-0503-2026
Foreign material. During production, the firm found pieces of blue plastic in a filter.
Class IIFDA: TerminatedVentura Foods LLC
FoodFeb 18, 2026
TKS Co-pack Manufacturing Aonic Complete His recall — FDA H-0521-2026
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
Class IIFDA: CompletedTKS Co-pack Manufacturing, LLC
FoodFeb 18, 2026
Ventura Foods CREAMY PEANUT BUTTER NET WT 1.12 OZ recall — FDA H-0504-2026
Foreign material. During production, the firm found pieces of blue plastic in a filter.
Class IIFDA: TerminatedVentura Foods LLC
FoodFeb 18, 2026
Karison brand PANJIRI recall — FDA H-0509-2026
Product contains milk, which is undeclared in the ingredient statement.
Class IIFDA: TerminatedKarison Foods & Snacks, Inc.
FoodFeb 18, 2026
TKS Co-pack Manufacturing Aonic Complete Hers recall — FDA H-0520-2026
Possible coliforms, E.coli, and/or Pseudomonas aeruginosa contamination.
Class IIFDA: CompletedTKS Co-pack Manufacturing, LLC
FoodFeb 18, 2026
Cacao Art Crunchy Caramel artisan dark chocolate with crunch brown sugar recall — FDA H-0498-2026
Undeclared allergen - milk. Product contains butter; cream is listed as a sub-ingredient of the butter, but milk is not declared in the ingredients or a contains statement.
Class IIFDA: TerminatedCacao Art
FoodFeb 18, 2026
KPCM New York a.) Preema brand Bright Red Food Colour Powder recall — FDA H-0490-2026
Products contain banned color, carmoisine and undeclared FD&C Yellow 5 and FD&C Red 40
Class IIFDA: OngoingKPCM New York Inc.
FoodFeb 18, 2026
MG Foods-Compass Group Spicy Breakfast Burrito in a flour tortilla recall — FDA H-0495-2026
foreign material (small hard plastic fragments)
Class IIFDA: TerminatedMG Foods-Compass Group
DrugFeb 18, 2026
Doxazosin Tablets, USP, 4 mg, 1000 tablets per bottle recall — FDA D-0306-2026
Tablets/Capsules Imprinted with Wrong ID
Class IIIFDA: OngoingUnichem Pharmaceuticals USA Inc.
DrugFeb 18, 2026
Oxycodone Hydrochloride Tablets, USP (CII), 5 mg, 100-Count (10 x 10) blister cards per recall — FDA D-0338-2026
Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.
Class IIFDA: OngoingAmerisource Health Services LLC
DrugFeb 18, 2026
UDENYCA recall — FDA D-0353-2026
Temperature Abuse. 116 cartons with specific serial numbers of Lot 2199821, were stored incorrectly in a controlled room temperature environment instead of the required refrigerated…
Class IFDA: OngoingMcKesson
VehicleFeb 12, 2026
Rogue throttlebody/manifold recall — NHTSA campaign 26V081000
Nissan North America, Inc. (Nissan) is recalling certain 2024-2025 Rogue vehicles equipped with 3-cylinder 1.5L variable compression turbo (VC-Turbo) engines. The gears in the electronic…
throttlebody/manifoldNissan North America, Inc.
VehicleFeb 12, 2026
Rogue hard parts internal/mechanical recall — NHTSA campaign 26V080000
Nissan North America, Inc. (Nissan) is recalling certain 2023-2025 Rogue vehicles equipped with 3-cylinder 1.5L variable compression turbo (VC-Turbo) engines. Increased temperatures can…
hard parts internal/mechanicalNissan North America, Inc.
VehicleFeb 12, 2026
General Motors control module software recall — NHTSA campaign 26V083000
General Motors, LLC is recalling certain 2020 Chevrolet Silverado 2500, 3500, GMC Sierra 2500, 3500, and 2020-2022 Chevrolet Silverado 1500 and GMC Sierra 1500 vehicles that may have been…
control module softwareGeneral Motors, LLC
Medical DeviceFeb 11, 2026
Changchun Wancheng Bio-Electron Co Vivoo Vaginal pH Test recall — FDA Z-1266-2026
Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or…
Class IIFDA: OngoingChangchun Wancheng Bio-Electron Co., Ltd.
Medical DeviceFeb 11, 2026
Vortex Surgical Lindsell Sutured IOL Marker, VS0390 - Scleral Marker recall — FDA Z-1256-2026
There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which…
Class IIFDA: OngoingVortex Surgical Inc.
Medical DeviceFeb 11, 2026
Changchun Wancheng Bio-Electron Co Menopause Test Cassette (Urine) recall — FDA Z-1260-2026
Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or…
Class IIFDA: OngoingChangchun Wancheng Bio-Electron Co., Ltd.
Medical DeviceFeb 11, 2026
da Vinci X, Xi Surgical System, & da Vinci 5 Surgical System recall — FDA Z-1232-2026
Due to a software implementation error that allowed instruments arms failing an important diagnostic test to remain in clinical use. This test was supposed to be used to detect Universal…
Class IIFDA: OngoingIntuitive Surgical, Inc.
Medical DeviceFeb 11, 2026
Fujirebio Diagnostics Lumipulse G pTau 217 Plasma Immunoreaction Cartridges recall — FDA Z-1302-2026
Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to…
Class IIFDA: OngoingFujirebio Diagnostics, Inc.
Medical DeviceFeb 11, 2026
Molift Mover 300 Model/Catalog Numbers: (1) M1501, (2) M1502, (3) M1504, (4) M15050, (5) recall — FDA Z-1309-2026
A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became…
Class IIFDA: OngoingETAC A/S
Medical DeviceFeb 11, 2026
Olympus Corporation of the Americas Single Use 3-Lumen Sphincterotome V (Distal Wire guided) recall — FDA Z-1283-2026
Devices which did not undergo thermoforming could deform and lose performance.
Class IIFDA: OngoingOlympus Corporation of the Americas
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
August 2026145 records · 4 categoriesJuly 2026369 records · 4 categoriesJune 2026373 records · 4 categoriesMay 2026330 records · 4 categoriesApril 2026407 records · 4 categoriesMarch 2026179 records · 4 categoriesFebruary 2026329 records · 4 categoriesJanuary 2026210 records · 4 categoriesDecember 2025184 records · 4 categoriesNovember 202596 records · 3 categoriesOctober 2025139 records · 3 categoriesSeptember 2025116 records · 3 categories