FoodJul 16, 2025
UNFI General Corporate 1 recall — FDA H-0242-2025
May be contaminated with fluid from a reach truck
Class IIFDA: TerminatedUNFI General Corporate
July 2025 recalls — page 7
These records include useful source details for the selected month.
FoodJul 16, 2025
UNFI General Corporate 1 recall — FDA H-0223-2025
May be contaminated with fluid from a reach truck
Class IIFDA: TerminatedUNFI General Corporate
FoodJul 16, 2025
UNFI General Corporate 1 recall — FDA H-0222-2025
May be contaminated with fluid from a reach truck
Class IIFDA: TerminatedUNFI General Corporate
FoodJul 16, 2025
Wegmans Food Markets a recall — FDA H-0219-2025
Product may contain foreign objects of metal origin.
Class IIFDA: TerminatedWegmans Food Markets, Inc.
FoodJul 16, 2025
Mellace Family Brands California Wegmans Semi-Sweet Chocolate Nonpareils, NET WT 18.5 OZ recall — FDA H-0278-2025
Undeclared milk
Class IIFDA: TerminatedMellace Family Brands California Inc.
FoodJul 16, 2025
Elwood International Calais Brand Grape jelly recall — FDA H-0252-2025
Contains undeclared colors (FD&C Blue 1 and FD&C Red 40)
Class IIIFDA: TerminatedElwood International, Inc.
DrugJul 16, 2025
KABANA SKIN CARE In Your Face Mineral Tint SPF 31, Zinc Oxide 25%, Tinted Sunscreen Broad recall — FDA D-0515-2025
cGMP deviations
Class IIFDA: OngoingKABANA SKIN CARE
DrugJul 16, 2025
KABANA SKIN CARE B Natural Organics, Organic Sunscreen, Broad Spectrum, SPF 30, 25% non-nano recall — FDA D-0512-2025
cGMP deviations
Class IIFDA: OngoingKABANA SKIN CARE
DrugJul 16, 2025
Duloxetine Delayed-Release Capsules, USP, 40mg, 30-count bottles recall — FDA D-0511-2025
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit
Class IIFDA: OngoingBreckenridge Pharmaceutical, Inc.
DrugJul 16, 2025
Famciclovir Tablets, USP 500 mg, 30-count bottles recall — FDA D-0509-2025
Presence of Foreign Substance- Black hair strand found attached to a tablet in a sealed bottle.
Class IIIFDA: OngoingMacleods Pharmaceuticals Ltd
DrugJul 16, 2025
KABANA SKIN CARE GreenScreen, kabana organic skincare, Bread Spectrum UVA & UVB, Zinc Oxide recall — FDA D-0514-2025
cGMP deviations
Class IIFDA: OngoingKABANA SKIN CARE
VehicleJul 11, 2025
Ford fuel injection system recall — NHTSA campaign 25V467000
Ford Motor Company (Ford) is recalling certain 2021-2024 Bronco Sport and 2020-2022 Escape vehicles equipped with 1.5L engines. A fuel injector may crack and leak fuel inside the engine…
fuel injection systemFord Motor Company
Medical DeviceJul 9, 2025
Siemens Healthcare Diagnostics ADVIA 120/2120/2120i SETpoint Calibrator recall — FDA Z-2086-2025
Products have the incorrect platelet (PLT) value assignments for the ADVIA 120/2120/2120i Hematology Systems.
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceJul 9, 2025
Philips S7-3t Transducer recall — FDA Z-2060-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Geneoscopy ColoSense Test Kit, Part No. 80-001, component of ColoSense test recall — FDA Z-2077-2025
Multiple plate failures documented as a result of the Low Positive Template Control being too high and out of range using the affected lot of ColoSense Test Kit.
Class IIFDA: OngoingGeneoscopy, Inc.
Medical DeviceJul 9, 2025
VITROS 5600 Integrated System recall — FDA Z-2038-2025
A software anomaly allows test results to be reported using Micro Tip and Micro Slide diluent packs that the system treats as expired even when the Use Expired Reagents setting is not…
Class IIFDA: OngoingOrtho-Clinical Diagnostics, Inc.
Medical DeviceJul 9, 2025
Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 recall — FDA Z-2045-2025
Medline Industries, LP. is issuing a recall for specific Medline kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN which was identified that during insertion of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceJul 9, 2025
Philips L9-3 Transducer recall — FDA Z-2057-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
VITROS 4600 Chemistry System recall — FDA Z-2040-2025
a software anomaly allows test results to be reported using Micro Tip and Micro Slide diluent packs that the system treats as expired even when the Use Expired Reagents setting is not…
Class IIFDA: OngoingOrtho-Clinical Diagnostics, Inc.
Medical DeviceJul 9, 2025
Siemens Medical Solutions USA ARTIS is a family of dedicated angiography systems developed recall — FDA Z-2019-2025
In very rare situations, communication between the sensor measuring dose applied to the area and the corresponding software fails. As a result of the failure, the system may incorrectly…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc.
Medical DeviceJul 9, 2025
Maquet Critical Care AB Servo-u MR Ventilator System recall — FDA Z-2015-2025
Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active…
Class IFDA: OngoingMaquet Critical Care AB
Medical DeviceJul 9, 2025
C.R. Bard BD Heyman Follower Coude Tip for following sizes: 12Fr - REF:021312 14Fr recall — FDA Z-2075-2025
Cather packaging may contain the incorrect French size.
Class IIFDA: OngoingC.R. Bard Inc.
Medical DeviceJul 9, 2025
Philips L8-4 Transducer recall — FDA Z-2056-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, Inc.
Medical DeviceJul 9, 2025
Philips VL13-5 Transducer recall — FDA Z-2063-2025
Ultrasound transducer devices were refurbished beyond their useful life.
Class IIFDA: OngoingPhilips Ultrasound, 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.