FoodSep 3, 2025
NEW ACAI AMAZONAS Organic Mango Freeze Dried Powder, Bulk, 15-kilogram boxes recall — FDA H-0538-2025
Potential Salmonella contamination
Class IFDA: TerminatedNEW ACAI AMAZONAS LLC
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 61
Records are ordered by the best available source date.
FoodSep 3, 2025
Bakers Authority Baker's Authority Graham Cracker Meal recall — FDA H-0535-2025
Product label does not list ingredients including major food allergens: wheat and soy (vegetable oil). Additional undeclared ingredients include: niacin, reduced iron, vitamin B1, vitamin…
Class IIFDA: OngoingBakers Authority LLC
FoodSep 3, 2025
Middlefield Original Cheese Cooperative 8 oz recall — FDA H-0530-2025
Potential contamination with Listeria monocytogenes
Class IFDA: TerminatedMiddlefield Original Cheese Cooperative
FoodSep 3, 2025
Middlefield Original Cheese Cooperative 8 oz recall — FDA H-0528-2025
Potential contamination with Listeria monocytogenes
Class IFDA: TerminatedMiddlefield Original Cheese Cooperative
FoodSep 3, 2025
Bakers Authority Baker's Authority Everything Bagel Mix recall — FDA H-0534-2025
Product label does not list ingredients including major food allergen: sesame. Additional undeclared ingredients include: poppy seeds, dried garlic, dried onion, and sea salt
Class IIFDA: OngoingBakers Authority LLC
FoodSep 3, 2025
Beaver Street Fisheries Great Value branded and Sea Best branded raw frozen shrimp in recall — FDA H-0549-2025
Product may be contaminated with Cesium-137 (Cs-137)
Class IIFDA: TerminatedBeaver Street Fisheries, Inc.
FoodSep 3, 2025
The J.M. Smucker Company Hostess Ding Dongs CHOCOLATE CAKE WITH CREAMY FILLING 2.55 oz recall — FDA H-0577-2025
Mold. The firm noticed an increase in customer complaints. They conducted a root cause investigation and discovered that one of their coolers had malfunctioning.
Class IIFDA: OngoingThe J.M. Smucker Company
FoodSep 3, 2025
Bakers Authority Baker's Authority Three Seed Mix recall — FDA H-0533-2025
Product label does not list ingredients including major food allergen: sesame. Additional undeclared ingredients include: millet and flax
Class IIFDA: OngoingBakers Authority LLC
FoodSep 3, 2025
H & N Group Frozen shrimp in bulk packaging recall — FDA H-0548-2025
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
Class IIFDA: TerminatedH & N Group Inc.
FoodSep 3, 2025
Gelsons Gelson's Hummus recall — FDA H-0526-2025
Gelson branded Hummus product labels do not include storage instructions "keep refrigerated"
Class IIFDA: TerminatedGelsons
DrugSep 3, 2025
Amerisource Health Services Sucralfate Tablets, USP 1 gram, 100 Tablets, (10x10) recall — FDA D-0598-2025
CGMP Deviations: The recalling firm filed for Chapter 11 in September 2024. As a result, it cannot monitor the quality program and hence cannot assure that products meet the identity,…
Class IIFDA: OngoingAmerisource Health Services LLC
DrugSep 3, 2025
Medline Alcohol Prep Pads, 70% Isopropyl Alcohol, 100 Sterile 2-Ply Pads, Single Use Only recall — FDA D-0600-2025
Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
DrugSep 3, 2025
Enoxaparin Sodium Injection, USP, 30 mg/0.3 mL recall — FDA D-0597-2025
Correct Labeled Product Mispack: Bags labeled for Enoxaparin Sodium Injection, 80 mg/0.8 mL, contained Enoxaparin Sodium Injection, 30 mg/0.3 mL
Class IIFDA: OngoingCardinal Health Inc.
DrugSep 3, 2025
CURAD Alcohol Prep Pads, Sterile, Medium, 2-Ply, Contents: 5 boxes per Carton, 30 Boxes per recall — FDA D-0601-2025
Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
DrugSep 3, 2025
Good Neighbor Pharmacy, Alcohol Prep Pads recall — FDA D-0604-2025
Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceAug 27, 2025
Immunotech A.S Estrone RIA Catalog Number DSL8700 UDI Code: 15099590211615 Estrone RIA is an recall — FDA Z-2336-2025
Estrone RIA kit lots may rarely give falsely high patient results which might cause Temporary injury of Remote probability or rarely give falsely low patient results which might cause…
Class IIFDA: OngoingImmunotech A.S.
Medical DeviceAug 27, 2025
Dynex Agility Sample Tips recall — FDA Z-2345-2025
The internal label affixed to the sample tip rack is incorrectly labeled as reagent tip racks. When scanned by the Agility instrument, the tip rack is misidentified as a different tip type,…
Class IIFDA: OngoingDynex Technologies, Inc.
Medical DeviceAug 27, 2025
Boston Scientific ENDOTAK RELIANCE G/SG, transvenous defibrillation lead, implantable recall — FDA Z-2325-2025
Affected lead models may experience gradually rising LVSI measurements in association with calcification of the defibrillation lead coils. The issue may lead to early lead replacement. Most…
Class IFDA: OngoingBoston Scientific Corporation
Medical DeviceAug 27, 2025
Ortho-Clinical Diagnostics VITROS Chemistry Products Ca Slides recall — FDA Z-2335-2025
Generations 67 and above of VITROS Ca Slides are experiencing an increased occurrence of Condition Code TH4-63J during calibration on VITROS XT 3400 and VITROS XT 7600 Systems, causing…
Class IIFDA: OngoingOrtho-Clinical Diagnostics, Inc.
Medical DeviceAug 27, 2025
Hamilton C6 REF 160021 recall — FDA Z-2328-2025
A mechanical defect on a printed circuit board (PCB) as a result of PCB separating process. This defect might cause the ventilator to either fail at startup (no patient involvement) or…
Class IFDA: OngoingHamilton Medical AG
Medical DeviceAug 27, 2025
Olympus Corporation of the Americas Electrosurgical, Cutting and Coagulation and Accessories recall — FDA Z-2339-2025
Potential for the ESG-410 Electrosurgical Generator to display an error message: "E0662 System Error", followed by either automatic single reboots of the device, or continuous reboot…
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceAug 27, 2025
Pentax Medical Video Processor recall — FDA Z-2329-2025
During endoscopic procedures using a combination of the video processor EPK-i8020c and i20c series video endoscope, the observed image can become reddish or dark. Users have observed smoke…
Class IIFDA: OngoingPentax of America Inc.
Medical DeviceAug 27, 2025
Boston Scientific RELIANCE 4-FRONT, endocardial cardioversion/defibrillation and pace/sense recall — FDA Z-2327-2025
Affected lead models may experience gradually rising LVSI measurements in association with calcification of the defibrillation lead coils. The issue may lead to early lead replacement. Most…
Class IFDA: OngoingBoston Scientific Corporation
Medical DeviceAug 27, 2025
Boston Scientific ENDOTAK RELIANCE G/SG with 4-SITE Connector, transvenous defibrillation recall — FDA Z-2326-2025
Affected lead models may experience gradually rising LVSI measurements in association with calcification of the defibrillation lead coils. The issue may lead to early lead replacement. Most…
Class IFDA: OngoingBoston Scientific Corporation
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.