FoodJul 2, 2025
P East Trading approximately 12 inches in length recall — FDA H-0067-2025
Clostridium botulinum (uneviscerated fish)
Class IFDA: TerminatedP East Trading Corp
Latest records
Latest recalls — page 207
The newest recall records with useful source details are listed here.
FoodJul 2, 2025
Isabelle's Kitchen Inc, Greek Pasta Salad, 4.5 lb., High density polyethylene recall — FDA H-0099-2025
Product has Salmonella contamination
Class IFDA: TerminatedIsabelle's Kitchen, Inc.
FoodJul 2, 2025
Target Grilled Chicken Greek Style Salad with Balsamic Dressing recall — FDA H-0064-2025
Cucumber in salad may be contaminated with Salmonella
Class IFDA: TerminatedTarget Corporation
FoodJul 2, 2025
Preventics, Inc. dba Legere Pharmaceuticals Super ProTHIN Plus, dietary supplement recall — FDA H-0092-2025
Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
Class IIIFDA: TerminatedPreventics, Inc. dba Legere Pharmaceuticals
FoodJul 2, 2025
FIREHOOK ARTISAN BAKED CRACKERS CLASSIC SEA SALT NET WT recall — FDA H-0065-2025
Undeclared Sesame. The firm was notified by a retailer that product labeled as Sea Salt Bagel Crackers contained Everything Bagel Crackers. The Everything Bagel Crackers contains sesame…
Class IIFDA: TerminatedFirehook of Virginia
FoodJul 2, 2025
Mightylicious Dairy-Free, Allergen Friendly, Egg-Free, Non-GMO, Kosher recall — FDA H-0066-2025
Undeclared Milk
Class IFDA: TerminatedMightylicious Inc.
FoodJul 2, 2025
Preventics, Inc. dba Legere Pharmaceuticals Probese Caps, dietary supplement with Iron recall — FDA H-0094-2025
Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
Class IIIFDA: TerminatedPreventics, Inc. dba Legere Pharmaceuticals
FoodJul 2, 2025
Preventics, Inc. dba Legere Pharmaceuticals Prothin, dietary supplement recall — FDA H-0091-2025
Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
Class IIIFDA: TerminatedPreventics, Inc. dba Legere Pharmaceuticals
FoodJul 2, 2025
Preventics, Inc. dba Legere Pharmaceuticals Rodex Forte, dietary supplement recall — FDA H-0096-2025
Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.
Class IIIFDA: TerminatedPreventics, Inc. dba Legere Pharmaceuticals
FoodJul 2, 2025
Element 112 1) Madeline's Patisserie 2.5 ounce Chocolate Croissant, Net Wt recall — FDA H-0058-2025
Undeclared wheat
Class IIFDA: TerminatedElement 112, LLC
FoodJul 2, 2025
MORTON SALT Windsor brand Extra Course Sea Salt Grinder Refill, 255 g recall — FDA H-0062-2025
The quantity of product in each unit does not match the stated weight.
Class IIIFDA: TerminatedMORTON SALT Inc.
FoodJul 2, 2025
TRI-UNION FROZEN PRODUCTS INC DBA CHICKEN OF THE Frozen Shrimp- packaged in 5lb frozen IQF recall — FDA H-0068-2025
Frozen Raw Peeled & Deveined tail on, shrimp contains undeclared sulfites
Class IFDA: TerminatedTRI-UNION FROZEN PRODUCTS INC DBA CHICKEN OF THE SEA…
FoodJul 2, 2025
Carley's Carley s Soft Baked Iced Lemon Cookies, 5.34oz Plastic Tray recall — FDA H-0088-2025
Product has a misbranded Yellow Color. Identified on label at Artificial Yellow Color , and it should be identified as FD&C Yellow #5
Class IIFDA: TerminatedCarley's Inc.
DrugJul 2, 2025
SODIUM CHLORIDE 0.9% Sodium Chloride Injection USP, 500 mL recall — FDA D-0491-2025
Lack of assurance of sterility: pinholes, within the finger boxes used during Form Fill Seal process resulting in leaks.
Class IIFDA: OngoingB BRAUN MEDICAL INC
DrugJul 2, 2025
Thrive Health and Wellness, LLC, dba Thrive LL Bioboost Injectable, Each 1mL contains recall — FDA D-0476-2025
Lack of Assurance of Sterility
Class IIFDA: OngoingThrive Health and Wellness, LLC, dba Thrive Health…
DrugJul 2, 2025
Thrive Health and Wellness, LLC, dba Thrive LX Bioboost Plus recall — FDA D-0477-2025
Lack of Assurance of Sterility
Class IIFDA: OngoingThrive Health and Wellness, LLC, dba Thrive Health…
DrugJul 2, 2025
DOBUTamine Injection, USP, 250 mg/20 mL (12.5 mg/mL), 20 mL per Single-dose Vial, carton of recall — FDA D-0489-2025
Discoloration; discolored solution from cracked vials
Class IIFDA: OngoingPfizer Inc.
VehicleJun 30, 2025
Volkswagen Group of service brakes recall — NHTSA campaign 25V434000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2023-2025 Atlas, Atlas Cross Sport and 2023-2024 ID.4 vehicles. Certain bolts on the chassis, brake system and/or…
service brakesVolkswagen Group of America, Inc.
VehicleJun 27, 2025
Nissan hard parts internal/mechanical recall — NHTSA campaign 25V437000
Nissan North America, Inc. (Nissan) is recalling certain 2021-2024 Rogue, 2019-2020 Altima, 2019-2022 Infiniti QX50, and 2022 Infiniti QX55 vehicles equipped with 3-cylinder 1.5L or…
hard parts internal/mechanicalNissan North America, Inc.
VehicleJun 27, 2025
Ford back over prevention software recall — NHTSA campaign 25V442000
Ford Motor Company (Ford) is recalling certain 2018-2022 Transit Connect, 2019-2020 MKZ, MKX, Edge, Continental, F-150, Nautilus, Fusion, 2019-2023 Ranger, Mustang, 2020-2021 EcoSport,…
back over prevention softwareFord Motor Company
VehicleJun 26, 2025
Chrysler fan/motor recall — NHTSA campaign 25V430000
Chrysler (FCA US, LLC) is recalling certain 2023 Jeep Grand Cherokee and Jeep Grand Cherokee L vehicles. The blower motor may fail, which can cause the defrosting and defogging system to be…
fan/motorChrysler (FCA US, LLC)
Medical DeviceJun 25, 2025
BALT USA Optima Coil System REFs/UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK recall — FDA Z-1988-2025
Due to radiopaque (RO) marker was not visible during angiography and it was determined that the RO marker was not manufactured to specification.
Class IIFDA: OngoingBALT USA, LLC
Medical DeviceJun 25, 2025
Dexcom G7 Glucose Receiver, SKUs (part number): STK-AT-011(MT26403-0), STK-AT-012 recall — FDA Z-1944-2025
Defective foam or an assembly error may cause the receiver speaker to lose contact with the printed circuit board, leading to missed audible alerts for low or high blood glucose values. A…
Class IFDA: OngoingDexcom, Inc.
Medical DeviceJun 25, 2025
Fresenius Medical Care Holdings 5008X HDF Hemodialysis Blood Tubing Set, 24 units per case recall — FDA Z-1992-2025
Potential of blood leak occurring between the lower port of the venous chamber and the tubing include: hemodiafiltration (HDF), hemodialysis (HD), hemofiltration (HF), and isolated…
Class IIFDA: OngoingFresenius Medical Care Holdings, Inc.
Browse by month
Recent recall archives
Browse recent months with enough recall history for useful comparison.
September 2026361 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 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categories