FoodAug 20, 2025
Jayone Foods Frozen Oyster Meat recall — FDA H-0501-2025
Frozen Oyster product is potentially contaminated with Norovirus
Class IIFDA: TerminatedJayone Foods, Inc.
Latest records
Latest recalls — page 139
The newest recall records with useful source details are listed here.
FoodAug 20, 2025
Shang Hao Jia Soda Biscuit recall — FDA H-0455-2025
Various snack cracker products are mislabeled and do not declare all allergen ingredients (Whole Milk Powder and wheat).
Class IIIFDA: TerminatedShang Hao Jia, Inc
FoodAug 20, 2025
QST Ingredients and Packaging Reduced Sodium Roast Beef Rub recall — FDA H-0495-2025
Product may contain small metal fragments due to contaminated onion powder ingredient used in manufacturing.
Class IIFDA: TerminatedQST Ingredients and Packaging
FoodAug 20, 2025
Quesito El Establo brand Spanish Cheese QUESITO COLOMBIANO recall — FDA H-0536-2025
Product was manufactured and held under insanitary conditions. Product may be contaminated with Listeria monocytogenes.
Class IFDA: TerminatedQuesito El Establo
FoodAug 20, 2025
Jagpreet Enterprises, LLC. dba Sukhi's Gourmet Sukhi's, TIKKA MASALA INDIAN CURRY SAUCE, NET recall — FDA H-0452-2025
Potential contamination with foreign objects (metal pieces).
Class IIFDA: TerminatedJagpreet Enterprises, LLC. dba Sukhi's Gourmet Indian…
FoodAug 20, 2025
Reser's Fine Foods net wt recall — FDA H-0541-2025
Tuna Salad products are recalled due to potential contamination with Listeria monocytogenes because products containing Newly Weds Foods recalled Japanese Style Breadcrumbs.
Class IFDA: TerminatedReser's Fine Foods, Inc.
FoodAug 20, 2025
Reser's Fine Foods Molly's Kitchens Tuna Salad, item 794599, net wt recall — FDA H-0545-2025
Tuna Salad products are recalled due to potential contamination with Listeria monocytogenes because products containing Newly Weds Foods recalled Japanese Style Breadcrumbs.
Class IFDA: TerminatedReser's Fine Foods, Inc.
DrugAug 20, 2025
Belsomra (suvorexant) tablets, 10mg, 30 Tablets in 3 Blister Cards per Carton, Each Blister recall — FDA D-0584-2025
Failed Dissolution Specifications: potential for delayed dissolution of the dose after administration which may result in delayed release of the drug, delaying onset of sleep.
Class IIFDA: OngoingMerck & Co. Inc
DrugAug 20, 2025
Carvedilol Tablets, USP, 25 mg, 500-count bottle recall — FDA D-0579-2025
CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity above the current Acceptable Intake Level.
Class IIFDA: OngoingGlenmark Pharmaceuticals Inc., USA
DrugAug 20, 2025
Westminster Pharmaceuticals Metoprolol Tartrate Tablets, USP, 50 mg, 1000 Tablets recall — FDA D-0581-2025
CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the established Acceptable Daily Intake (ADI) level.
Class IIFDA: OngoingWestminster Pharmaceuticals LLC
DrugAug 20, 2025
Westminster Pharmaceuticals Metoprolol Tartrate Tablets, USP, 100 mg, 1000 Tablets recall — FDA D-0582-2025
CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the established Acceptable Daily Intake (ADI) level.
Class IIFDA: OngoingWestminster Pharmaceuticals LLC
DrugAug 20, 2025
Carvedilol Tablets, USP, 3.125 mg, Packaged as: a)500-count bottle, NDC 68462-162-05 recall — FDA D-0577-2025
CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity above the current Acceptable Intake Level.
Class IIFDA: OngoingGlenmark Pharmaceuticals Inc., USA
DrugAug 20, 2025
Theophylline extended-release tablets 400mg, 100-count bottle recall — FDA D-0583-2025
Failed Dissolution Specifications: Failure results (above) were reported for the Dissolution (by UV) test for commercial annual stability at the long-term shelf life stability interval,…
Class IIFDA: OngoingGlenmark Pharmaceuticals Inc., USA
DrugAug 20, 2025
Carvedilol Tablets, USP, 12.5 mg, 500 Tablets per carton recall — FDA D-0587-2025
CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity observed to be above the FDA-recommended limit of NMT 4.0 ppm
Class IIFDA: OngoingGlenmark Pharmaceuticals Inc., USA
DrugAug 20, 2025
Lactated Ringer's Injection USP, L 7500, 1000mL Excel Container recall — FDA D-0585-2025
Lack of Assurance of Sterility; potential for fluid leakage at one of the weld sites.
Class IIFDA: OngoingB BRAUN MEDICAL INC
DrugAug 20, 2025
Carvedilol Tablets, USP, 25 mg, 500 Tablets per carton recall — FDA D-0588-2025
CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity observed to be above the FDA-recommended limit of NMT 4.0 ppm
Class IIFDA: OngoingGlenmark Pharmaceuticals Inc., USA
DrugAug 20, 2025
Duloxetine Delayed-Release Capsules, USP, 60 mg, 1,000 Capsules per bottle recall — FDA D-0580-2025
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.
Class IIFDA: OngoingBreckenridge Pharmaceutical, Inc.
DrugAug 20, 2025
Carvedilol Tablets, USP, 12.5 mg, 500-count bottle recall — FDA D-0578-2025
CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity above the current Acceptable Intake Level.
Class IIFDA: OngoingGlenmark Pharmaceuticals Inc., USA
DrugAug 20, 2025
SODIUM CHLORIDE 0.9% Sodium Chloride Injection USP, L 8000, 1000mL Excel Container recall — FDA D-0586-2025
Lack of Assurance of Sterility; potential for fluid leakage at one of the weld sites.
Class IIFDA: OngoingB BRAUN MEDICAL INC
VehicleAug 18, 2025
Chrysler instrument cluster/panel recall — NHTSA campaign 25V530000
Chrysler (FCA US, LLC) is recalling certain 2026 Ram 3500, 3500 Cab Chassis, 2500, 4500 Cab Chassis, and 5500 Cab Chassis vehicles. The instrument panel may display an incorrect brake…
instrument cluster/panelChrysler (FCA US, LLC)
VehicleAug 14, 2025
Jeep Wrangler pressure monitoring and regulating systems recall — NHTSA campaign 25V527000
Chrysler (FCA US, LLC) is recalling certain 2024-2025 Jeep Wrangler vehicles. The remote start antenna cable may be pinched, which can cause the tire pressure monitoring system (TPMS)…
pressure monitoring and regulating systemsChrysler (FCA US, LLC)
VehicleAug 13, 2025
Tiguan tie rod recall — NHTSA campaign 25V526000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2025 Tiguan vehicles. A tie rod bolt on the rear axle assembly may be loose, which can lead to a loss of vehicle control.
tie rodVolkswagen Group of America, Inc.
FoodAug 13, 2025
GIVE AND GO PREPARED FOODS Favorite Day Bakery Frosted Sugar Cookies, 10 count, Net Wt recall — FDA H-0385-2025
Foreign Material (wood)
Class IIFDA: TerminatedGIVE AND GO PREPARED FOODS CORP
FoodAug 13, 2025
Navarro Pecan Holdings FANCY MEDIUM PECAN PIECES 81124 561958 554707 6/13/2025 recall — FDA H-0379-2025
Pecans have the potential to be contaminated with Salmonella,
Class IFDA: OngoingNavarro Pecan Holdings, LLC
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Recent recall archives
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August 2026148 records · 4 categoriesJuly 2026369 records · 4 categoriesJune 2026374 records · 4 categoriesMay 2026336 records · 4 categoriesApril 2026408 records · 4 categoriesMarch 2026182 records · 4 categoriesFebruary 2026330 records · 4 categoriesJanuary 2026211 records · 4 categoriesDecember 2025382 records · 4 categoriesNovember 2025275 records · 4 categoriesOctober 2025143 records · 3 categoriesSeptember 2025118 records · 3 categories