FoodOct 22, 2025
Garden Fresh Foods Sliced recall — FDA H-0035-2026
Possible positive Listeria monocytogenes. Firm tested one lot of sliced green onions in-house and found Listeria monocytogenes.
Class IFDA: TerminatedGarden Fresh Foods, Inc.
October 2025 recalls — page 11
These records include useful source details for the selected month.
FoodOct 22, 2025
WHOLESALE PRODUCE SUPPLY LLC DBA Cut Fresh Fruit with Fruit Dip recall — FDA H-0064-2026
Potential Listeria monocytogenes contamination.
Class IFDA: TerminatedWHOLESALE PRODUCE SUPPLY LLC DBA
FoodOct 22, 2025
Black Sheep Egg Company Free Range Grade AA Large Brown Eggs, Loose Open Skid, 900dz recall — FDA H-0051-2026
Potential Salmonella contamination.
Class IFDA: TerminatedBlack Sheep Egg Company, LLC
FoodOct 22, 2025
WHOLESALE PRODUCE SUPPLY LLC DBA Cut Fresh Cantaloupe Chunks packaged into the following recall — FDA H-0059-2026
Potential Listeria monocytogenes contamination.
Class IFDA: TerminatedWHOLESALE PRODUCE SUPPLY LLC DBA
FoodOct 22, 2025
Goyal Group 1 recall — FDA H-0058-2026
Contains elevated levels of lead
Class IIFDA: TerminatedGoyal Group Inc.
FoodOct 22, 2025
Pacific Coast Producers Halved Pears IN PEAR JUICE FROM CONCNETRATE recall — FDA H-0039-2026
Potential contamination with heavy metal (Lead).
Class IIFDA: CompletedPacific Coast Producers
FoodOct 22, 2025
Black Sheep Egg Company Free Range Grade AA Medium White Eggs, Loose Open Skid, 900dz recall — FDA H-0054-2026
Potential Salmonella contamination.
Class IFDA: TerminatedBlack Sheep Egg Company, LLC
FoodOct 22, 2025
Sprout Organics Apple & Spinach NET WT recall — FDA H-0134-2026
Potential contamination with heavy metal (Lead).
Class IIFDA: OngoingSprout Organics Inc.
FoodOct 22, 2025
TROPICANA BRANDS GROUP Dole Apple Juice recall — FDA H-0073-2026
A manufacturing process deviation occurred which may cause spoilage or microbial contamination and affect shelf stability.
Class IIFDA: TerminatedTROPICANA BRANDS GROUP
FoodOct 22, 2025
Black Sheep Egg Company Free Range Grade AA Medium Brown Eggs, Loose Pack in Boxes recall — FDA H-0050-2026
Potential Salmonella contamination.
Class IFDA: TerminatedBlack Sheep Egg Company, LLC
FoodOct 22, 2025
Black Sheep Egg Company Free Range Grade A Large Brown Eggs, 12ct Cartons, UPC recall — FDA H-0047-2026
Potential Salmonella contamination.
Class IFDA: TerminatedBlack Sheep Egg Company, LLC
FoodOct 22, 2025
WHOLESALE PRODUCE SUPPLY LLC DBA Cut Fresh Fruit Mix recall — FDA H-0068-2026
Potential Listeria monocytogenes contamination.
Class IFDA: TerminatedWHOLESALE PRODUCE SUPPLY LLC DBA
DrugOct 22, 2025
SV Labs Prescott Aloe Up Sport Performance Sunscreen Lotion SPF 30, 1 FL OZ (30 mL) per recall — FDA D-0022-2026
cGMP deviations: the firm released and distributed product which failed total aerobic microbial count testing.
Class IIFDA: OngoingSV Labs Prescott Corporation
DrugOct 22, 2025
VIORELE recall — FDA D-0021-2026
Failed Impurities/Degradation Specifications
Class IIFDA: OngoingGlenmark Pharmaceuticals Inc., USA
DrugOct 22, 2025
Atorvastatin Calcium Tablets USP, 10 mg recall — FDA D-0017-2026
Failed Dissolution Specifications
Class IIFDA: OngoingAscend Laboratories, LLC
DrugOct 22, 2025
IntegraDose Compounding Services Oxytocin 30 Units/500 mL in 0.9% Sodium Chloride for recall — FDA D-0015-2026
Subpotent Drug: Testing revealed there was no oxytocin in the IV bag.
Class IFDA: OngoingIntegraDose Compounding Services LLC
DrugOct 22, 2025
Amerisource Health Services Sucralfate Tablets, USP 1 gram, 100 Tablets, (10x10) recall — FDA D-0027-2026
CGMP Deviations: The recalling firm filed for Chapter 11 on September 30, 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
DrugOct 22, 2025
Carbidopa, Levodopa, Entacapone Tablets, 25 mg/100 mg/200 mg, 100-count bottle recall — FDA D-0029-2026
Product mix up: complaint received that sealed medication bottle contained Carbidopa, Levodopa, and Entacapone film-coated tablets (37.5 mg/150 mg/200 mg) instead of labelled lower strength…
Class IIFDA: OngoingRising Pharma Holding, Inc.
VehicleOct 21, 2025
BMW retractor recall — NHTSA campaign 25V717000
BMW of North America, LLC is recalling certain 2026 2 Series Gran Coupe, X1, X2, and Mini Countryman S ALL4 vehicles. The housing pin in the rear (left and/or right) seat belt retractors…
retractorBMW of North America, LLC
Medical DeviceOct 15, 2025
B BRAUN MEDICAL PERIFIX FX Continuous Epidural Anesthesia Set, PERIFIX Tuohy Epidural Needle recall — FDA Z-0121-2026
Potential for the lid of the catheter connector to be in the incorrect position.
Class IIFDA: OngoingB BRAUN MEDICAL Inc.
Medical DeviceOct 15, 2025
NOXBOX recall — FDA Z-0029-2026
The unexpected internal fault / system diagnostic error to result when a rapid succession of button selections is made to the user interface without waiting for the device to respond to…
Class IFDA: OngoingNOXBOX LTD
Medical DeviceOct 15, 2025
LeMaitre Vascular Artegraft Collagen Vascular Graft recall — FDA Z-0072-2026
Devices were distributed with incorrect label without CE and UKCA mark, missing patient leaflet and patient implant card.
Class IIFDA: OngoingLeMaitre Vascular, Inc.
Medical DeviceOct 15, 2025
Applied Medical Technology NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x recall — FDA Z-0128-2026
The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
Class IIFDA: CompletedApplied Medical Technology Inc.
Medical DeviceOct 15, 2025
Applied Medical Technology NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x recall — FDA Z-0130-2026
The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
Class IIFDA: CompletedApplied Medical Technology Inc.
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.