FoodSep 10, 2025
The Candy Barn Chocolate Fudge, The Candy Barn, 1113 Palm Ave Riverside, IA recall — FDA H-0559-2025
Allergen labeling: egg is not listed in the 'contains' statement
Class IIFDA: TerminatedThe Candy Barn
Latest records
Latest recalls — page 179
The newest recall records with useful source details are listed here.
FoodSep 10, 2025
The Candy Barn Grandma's Old-Fashioned Peanut Brittle, The Candy Barn, 1113 recall — FDA H-0566-2025
Allergen labeling: missing allergens (peanuts, milk) in contains statement
Class IIFDA: TerminatedThe Candy Barn
FoodSep 10, 2025
TAMPA MAID FOODS ADMIRAL OF THE FLEET and PORTICO SEAFOOD CLASSIC recall — FDA H-0552-2025
Product may be contaminated with Cesium-137 (Cs-137)
Class IIFDA: TerminatedTAMPA MAID FOODS, LLC
FoodSep 10, 2025
TAMPA MAID FOODS Clean-tail Coconut Farm Raise Breaded Butterfly Shrimp Clean recall — FDA H-0553-2025
Product may be contaminated with Cesium-137 (Cs-137)
Class IIFDA: TerminatedTAMPA MAID FOODS, LLC
DrugSep 10, 2025
IMMUNOCORE KIMMTRAK (tebentafusp-tebn) Injection, 100 mcg/0.5 mL, For intravenous Infusion recall — FDA D-0614-2025
Subpotent Drug
Class IIFDA: OngoingIMMUNOCORE, LLC
DrugSep 10, 2025
chlorproMAZINE Hydrochloride Tablets, USP, 50 mg, 100-count bottle recall — FDA D-0617-2025
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any…
Class IIFDA: OngoingAmneal Pharmaceuticals, LLC
DrugSep 10, 2025
DermaRite Industries KleenFoam, Antimicrobial Foam Soap with Aloe Vera, (Chloroxylenol 0.5%) recall — FDA D-0612-2025
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
Class IFDA: OngoingDermaRite Industries, LLC
DrugSep 10, 2025
Sulfamethoxazole and Trimethoprim Tablets, USP 800mg/160mg, Double Strength recall — FDA D-0615-2025
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any…
Class IIFDA: OngoingAmneal Pharmaceuticals, LLC
DrugSep 10, 2025
DermaRite Industries DermaKleen, Health Care Antiseptic Lotion Soap with Vitamin E recall — FDA D-0610-2025
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
Class IFDA: OngoingDermaRite Industries, LLC
DrugSep 10, 2025
chlorproMAZINE Hydrochloride Tablets, USP, 25 mg, 100-count bottles recall — FDA D-0616-2025
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any…
Class IIFDA: OngoingAmneal Pharmaceuticals, LLC
DrugSep 10, 2025
chlorproMAZINE Hydrochloride Tablets, USP, 100 mg, 100-count bottle recall — FDA D-0618-2025
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any…
Class IIFDA: OngoingAmneal Pharmaceuticals, LLC
DrugSep 10, 2025
chlorproMAZINE Hydrochloride Tablets, USP, 200 mg, 100-count bottles recall — FDA D-0619-2025
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any…
Class IIFDA: OngoingAmneal Pharmaceuticals, LLC
DrugSep 10, 2025
DermaRite Industries DermaSarra, External Analgesic, (Camphor 0.5%) 222 mL (7.5 fl. oz.) per recall — FDA D-0611-2025
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
Class IFDA: OngoingDermaRite Industries, LLC
DrugSep 10, 2025
DermaRite Industries PeriGiene, Health Care Antiseptic, (Chloroxylenol 0.5%) 222 mL recall — FDA D-0613-2025
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
Class IFDA: OngoingDermaRite Industries, LLC
VehicleSep 5, 2025
Acura RDX electric power assist system recall — NHTSA campaign 25V582000
Honda (American Honda Motor Co.) is recalling certain 2025 Acura RDX vehicles. The software for the electric power steering (EPS) assist may not be calibrated properly, which can cause the…
electric power assist systemHonda (American Honda Motor Co.)
VehicleSep 4, 2025
Ford camera recall — NHTSA campaign 25V572000
Ford Motor Company (Ford) is recalling certain 2015-2019 Lincoln MKC, Mustang, F-350 SD, F-250 SD, F-450 SD, 2015-2017 Lincoln Navigator, Expedition, 2015-2018 Edge, Transit Connect,…
cameraFord Motor Company
VehicleSep 4, 2025
Chrysler propulsion electrical system recall — NHTSA campaign 25V576000
Chrysler (FCA US, LLC) is recalling certain 2022-2026 Jeep Grand Cherokee Plug-In Hybrid Electric (PHEV) vehicles. A software error within the hybrid control processor may result in a loss…
propulsion electrical systemChrysler (FCA US, LLC)
Medical DeviceSep 3, 2025
CareFusion 303 BD Pyxis Product Name / UDI-DI code / Catalog No recall — FDA Z-2477-2025
Antivirus software was not consistently installed on impacted devices during the implementation process.
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceSep 3, 2025
Orascoptic Superior Visualization Phantom Essential kit recall — FDA Z-2443-2025
Due to complaints, loupe nose pads containing nickel may cause an allergic reaction.
Class IIFDA: OngoingOrascoptic Surgical Acuity
Medical DeviceSep 3, 2025
VANTIVE US HEALTHCARE PrisMax V3 control Unit-US, Hemodialysis Delivery System, Product Code recall — FDA Z-2438-2025
Unexpected PrisMax System alarm T0830: Blood Leak Detected, when no blood leak is present, or difficulty normalizing the Blood Leak Detector (BLD) leading to PrisMax System alarms T1313:…
Class IIFDA: OngoingVANTIVE US HEALTHCARE LLC
Medical DeviceSep 3, 2025
AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) ROBOT HYST PACK recall — FDA Z-2471-2025
During an internal investigation, ACS determined that the rationale for sterilization of certain components was not justified and therefore, some components are not fit for further…
Class IIFDA: OngoingAmerican Contract Systems Inc.
Medical DeviceSep 3, 2025
Orascoptic Superior Visualization Custom loupes configured with Phantom Frames recall — FDA Z-2441-2025
Due to complaints, loupe nose pads containing nickel may cause an allergic reaction.
Class IIFDA: OngoingOrascoptic Surgical Acuity
Medical DeviceSep 3, 2025
Onkos Surgical ELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS BOWED CANAL FILLING STEMS recall — FDA Z-2423-2025
Unidentified substance of unknown impact was identified on devices during a retrospective evaluation.
Class IIFDA: OngoingOnkos Surgical, Inc.
Medical DeviceSep 3, 2025
Onkos Surgical ELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS SEGMENTAL STEM CANAL FILLING recall — FDA Z-2424-2025
Unidentified substance of unknown impact was identified on devices during a retrospective evaluation.
Class IIFDA: OngoingOnkos Surgical, Inc.
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