FoodApr 2, 2025
Liaoning Cheng Da (USA) Wangzhine branded Hot Pot Sauce recall — FDA F-0672-2025
(Imported) Hot Pot Sauce contains undeclared allergens (Wheat and Soy)
Class IFDA: TerminatedLiaoning Cheng Da (USA) Inc.
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 124
Records are ordered by the best available source date.
FoodApr 2, 2025
Paletas Ice Cream Flor de Michoacan Blue Hawaiian Artificially Flavored Beverage recall — FDA F-0670-2025
Undeclared Red #3
Class IIIFDA: TerminatedPaletas Ice Cream, LLC
FoodApr 2, 2025
U.S. Tov, Inc. dba U.S. Trading Company DRIED LILY FLOWERS Net Weight 2.5 oz recall — FDA F-0668-2025
Undeclared sulfites
Class IIIFDA: TerminatedU.S. Tov, Inc. dba U.S. Trading Company
FoodApr 2, 2025
Great Lakes Coca-Cola Distribution Coco-Cola Original Taste, 12 Fl Oz recall — FDA F-0664-2025
Foreign object (plastic)
Class IIFDA: TerminatedGreat Lakes Coca-Cola Distribution LLC
DrugApr 2, 2025
QuVa Pharma fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.2% ROPivacaine HCl 200 mg/100 recall — FDA D-0297-2025
Lack of Assurance of Sterility
Class IIFDA: OngoingQuVa Pharma, Inc.
DrugApr 2, 2025
Johnson, S C and Son babyganics, Sheer Blend, SPF 50 Mineral Sunscreen Fragrance Free recall — FDA D-0298-2025
Failed stability specifications: during routine stability monitoring quality concerns were identified. Physical separation for ingredients was observed.
Class IIFDA: OngoingJohnson, S C and Son, Inc
DrugApr 2, 2025
Ascent Consumer Products SinuCleanse Premixed SALINE PACKETS recall — FDA D-0300-2025
Microbial Contamination of Non-Sterile Products: Bacterial contamination with Staphylococcus aureus
Class IFDA: OngoingAscent Consumer Products Inc.
DrugApr 2, 2025
QuVa Pharma fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.1% Bupivacaine HCl 100 mg/100 recall — FDA D-0295-2025
Lack of Assurance of Sterility
Class IIFDA: OngoingQuVa Pharma, Inc.
DrugApr 2, 2025
Ascent Consumer Products SinuCleanse Soft Tip NETI POT Nasal Wash System recall — FDA D-0301-2025
Microbial Contamination of Non-Sterile Products: Bacterial contamination with Staphylococcus aureus
Class IFDA: OngoingAscent Consumer Products Inc.
DrugApr 2, 2025
Ascent Consumer Products SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System recall — FDA D-0299-2025
Microbial Contamination of Non-Sterile Products: Bacterial contamination with Staphylococcus aureus
Class IFDA: OngoingAscent Consumer Products Inc.
DrugApr 2, 2025
SODIUM BICARBONATE 8.4% Sodium Bicarbonate Injection, USP, 50 mEq/50 mL (1 mEq/mL), 25 x 50 recall — FDA D-0303-2025
Lack of Assurance of Sterility
Class IIFDA: OngoingExela Pharma Sciences LLC
DrugApr 2, 2025
HYDROGEN PEROXIDE [CORRECT FRONT PANEL] Hydrogen Peroxide Topical Solution, USP, 32 FL OZ recall — FDA D-0302-2025
Labeling; Label Mixup; some bottles have an incorrect back label indicating 91% Isopropyl Alcohol
Class IIFDA: OngoingConsumer Product Partners, LLC
DrugApr 2, 2025
QuVa Pharma fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.125% Bupivacaine HCl 125 mg/100 recall — FDA D-0296-2025
Lack of Assurance of Sterility
Class IIFDA: OngoingQuVa Pharma, Inc.
VehicleApr 1, 2025
BMW starter motor recall — NHTSA campaign 25V202000
BMW of North America, LLC (BMW) is recalling certain 2025 330i, 330i xDrive, 530i, 530i xDrive, 4 Series Coupe (430i, 430i xDrive), 4 Series Convertible (430i, 430i xDrive), 4 Series Gran…
starter motorBMW of North America, LLC
VehicleMar 31, 2025
Volkswagen Group of instrument cluster/panel recall — NHTSA campaign 25V201000
Volkswagen Group of America, Inc. (Audi) is recalling certain 2021 SQ8, A6 SEDAN, A7, A8, Q7, Q8, RS6 Avant, RS7, RSQ8, S6 SEDAN, S7, S8, A6 Allroad, and SQ7 vehicles. Due to a software…
instrument cluster/panelVolkswagen Group of America, Inc.
VehicleMar 28, 2025
Ford oil/lubrication recall — NHTSA campaign 25V198000
Ford Motor Company (Ford) is recalling certain 2024-2025 F-150, Expedition, and 2024 Lincoln Navigator vehicles equipped with 3.5L GTDI engines. The engine may have a misaligned engine cup…
oil/lubricationFord Motor Company
Medical DeviceMar 26, 2025
Merge Healthcare VERICIS, Merge Cardio recall — FDA Z-1400-2025
When following a specific less typical workflow in which the user remeasures using the ultrasound device or manually edits primitive or derived measurement values directly in Clinical…
Class IIFDA: OngoingMerge Healthcare, Inc.
Medical DeviceMar 26, 2025
smiths medical ProPort Plastic Venous Access System, PolyFlow Polyurethane Catheter, 1.9mm recall — FDA Z-1280-2025
The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect.
Class IFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceMar 26, 2025
Oridion Medical 1987 Microstream Instructions for Use and Part Number used with - Product recall — FDA Z-1376-2025
Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2 Oral-Nasal Filter Line/Intubated Filter (CO2) Line device users may experience difficulty/inability to disconnect…
Class IIFDA: OngoingOridion Medical 1987 Ltd.
Medical DeviceMar 26, 2025
Beckman Coulter DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137 recall — FDA Z-1388-2025
the DxI 9000 encoder wheel was misaligned on the motor shaft, leading to increased slippage errors and causing the instrument to stop, posing a high safety risk due to potential delays in…
Class IIFDA: OngoingBeckman Coulter, Inc.
Medical DeviceMar 26, 2025
B Braun Medical Introcan Safety 3 Closed IV Catheter 22 Ga. x 1 in., PUR, Winged recall — FDA Z-1397-2025
Increased risk for valve housing detachment causing leakage.
Class IIFDA: OngoingB Braun Medical Inc.
Medical DeviceMar 26, 2025
Waldemar Link GmbH & Co. KG Modular Stem cylindrical, Tilastan, press-fit cementless, L= 80 recall — FDA Z-1373-2025
A problem was discovered during the scanning process of the outer carton label because of an incorrect GTIN on the label, which is a GTIN for a different product.
Class IIFDA: OngoingWaldemar Link GmbH & Co. KG (Mfg Site)
Medical DeviceMar 26, 2025
MEDLINE INDUSTRIES, LP - Northfield Proxima Drape labeled as DRAPE C-SECTION W/ WINDOW recall — FDA Z-1363-2025
Potential breach in pouch packaging which could lead to loss of sterility.
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceMar 26, 2025
Medline procedure kits labeled as: 1) C SECTION, Pack Number DYNJ909098 recall — FDA Z-1393-2025
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
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.