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
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 41
Records are ordered by the best available source date.
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.
Medical DeviceOct 15, 2025
FUJIFILM Healthcare Americas FDR Visionary Suite, CH-200 Model/Version Numbers: (1) recall — FDA Z-0044-2026
It was found that the shaft for mounting the X-ray tube unit on the support may break. In addition, it was found that the protective parts might not work effectively only when the shaft was…
Class IIFDA: OngoingFUJIFILM Healthcare Americas Corporation
Medical DeviceOct 15, 2025
B BRAUN MEDICAL PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 recall — FDA Z-0117-2026
Potential for the lid of the catheter connector to be in the incorrect position.
Class IIFDA: OngoingB BRAUN MEDICAL Inc.
Medical DeviceOct 15, 2025
Fresenius Medical Care Holdings Optiflux High Flux E-beam Dialyzer Model Numbers: (1) recall — FDA Z-0041-2026
To provide further information to the user to ensure proper use of the medical device. the caps had been changed from a threaded version to a press-on version whereby the user must press…
Class IIFDA: OngoingFresenius Medical Care Holdings, Inc.
Medical DeviceOct 15, 2025
B BRAUN MEDICAL PERIFIX FX Continuous Epidural Anesthesia Tray, 17 Ga. x 3-1/2 in. (8.9 cm) recall — FDA Z-0118-2026
Potential for the lid of the catheter connector to be in the incorrect position.
Class IIFDA: OngoingB BRAUN MEDICAL Inc.
Medical DeviceOct 15, 2025
B BRAUN MEDICAL PERIFIX FX Continuous Epidural Anesthesia Tray, PERIFIX 17 Ga. x 3-1/2 in. recall — FDA Z-0119-2026
Potential for the lid of the catheter connector to be in the incorrect position.
Class IIFDA: OngoingB BRAUN MEDICAL Inc.
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.