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Consumer Product Recalls
127,502 recalls from the U.S. Consumer Product Safety Commission, newest first.
January 15, 2025Medical DevicesFDA
Aerin Medical, Inc. recalls Aerin Medical VivAer Stylus, REF CAT1785 (individual stylus), and REF CAT500 (5-pack), sterile.
Hazard: Some units in a single production lot were programmed incorrectly which will result in the VivAer Stylus being incorrectly recognized as RhinAer Stylus when connected to the Aerin Console.
January 15, 2025Medical DevicesFDA
Stryker Corporation recalls 100V NEPTUNE 3 ROVER JAPANESE (0703-003-000) 120V NEPTUNE S ROVER (0711-001-000) 230V NEPTUNE 3 ROVER ENGLISH (0703-00
Hazard: Bolts on the vacuum pump filter housing and the flange plate were not properly tightened, impacting the function of the Neptune rovers. Systems with loose bolts may fail to provide sufficient suction force or loss of suction during a procedure.
January 15, 2025Medical DevicesFDA
Elucent Medical Inc recalls EnVisio Patient Pad Transition Cushion, Model/Catalog Number: ENVISIO-SYS Product Description: The EnVisio Patient Pad
Hazard: There is a potential safety risk caused by physical disassociation of the back section from the bed frame of Skytron model series 3600, 6500, 6600 and 6700 operating room beds when used with the EnVisio Navigation System.
January 15, 2025Medical DevicesFDA
Qualigen Inc recalls The FastPack IP Sex Hormone Binding Globulin Immunoassay, Part #25000081, is for the quantitative measurement of SHBG in
Hazard: Three lots of the FastPacks kitted into the FastPack SHBG Complete Kits were labeled with the incorrect expiration date. The following is a listing of affected lots: Lot Number: 2408018-1, 2409015-1, and 2409015-2. The likelihood of patient harm is expected to be low as routine Quality Control should detect kits that are impacted by signal deterioration due to age.
January 15, 2025Medical DevicesFDA
IDS LTD recalls Smaxel Fractional CO2 Laser, a Class IV medical laser system.
Hazard: The Smaxel Fractional CO2 Laser does not include a Certification label, and adequate instructions for safe operation of the device.
January 15, 2025Medical DevicesFDA
Beckman Coulter, Inc. recalls Access Intact PTH assay, a paramagnetic particle, chemiluminescent immunoassay for the quantitative determination of int
Hazard: Beckman Coulter has identified that some Access PTH reagent packs from lot 339071 may be over- or under-filled in well 0. The dispensed material in well 0 could be above or below specification, risking sealing issues, contamination, instrument errors, delays, or inaccurate results with a negative bias and increase in imprecision. The issue was confirmed on 10 April 2024 by Beckman Coulter through an internal non-conformance (NC-INT-66585). The well 0 scale on the filling line began malfunctioning on the fill immediately before PTH. The malfunction was not noticed until the majority of PTH was filled.
January 15, 2025Medical DevicesFDA
Greiner Bio-One GmbH recalls VACUETTE SAFELINK, REF: 450210
Hazard: The VACUETTE SAFELINK Holder with male luer lock may leak blood due to the protective rubber sleeve bunching up and not retracting when using the device.
January 15, 2025Medical DevicesFDA
Fresenius Medical Care Holdings, Inc. recalls Dialyzer Optiflux 160NRe
Hazard: Potential for internal blood leaks due to cracked polyurethane
January 15, 2025Medical DevicesFDA
JIANGSU JUMAO X-CARE MEDICAL EQUIPMENT CO LTD recalls JMC5A Ni/TruAire-5 Oxygen Concentrator, Model: O2C5L
Hazard: Oxygen concentrator may melt or catch on fire during use.
January 15, 2025Medical DevicesFDA
Fresenius Kabi USA, LLC recalls Ivenix Infusion System (IIS), Large Volume Pump, Model Number: LVP-0004
Hazard: Potential pneumatic valve failure that may cause the LVP to stop an active infusion and/or could prevent the pump from being used.
January 15, 2025Medical DevicesFDA
Maquet Cardiovascular, LLC recalls Vasoview Hemopro 2 (w/Vasoshield) Endoscopic Vessel Harvesting System. Model Numbers: VH-4001. Indicated for use in min
Hazard: Potential for two issues: 1. Bent or detached heater wire; 2. Silicone peeling or detaching from the Jaws of the Harvesting Tool
January 15, 2025Medical DevicesFDA
Maquet Cardiovascular, LLC recalls VasoView HemoPro 2 Endoscopic Vessel Harvesting System. Model Numbers: VH-4000. Indicated for use in minimally invasive
Hazard: Potential for two issues: 1. Bent or detached heater wire; 2. Silicone peeling or detaching from the Jaws of the Harvesting Tool
January 15, 2025Food & BeverageFDA
TREE HOUSE FOODS INC recalls Great Value, Chicken Broth, 48 oz. , Aseptic paper cartons, 6 retail units per case, 120 cases/pallet .
Hazard: Potential for packaging failures that could compromise the sterility of the product, resulting in spoilage.
January 15, 2025Food & BeverageFDA
HP Hood (VERNON) recalls WELLSLEY FARM PLAIN NON-FAT GREEK YOGURT; 40 oz; UPC 888670048085
Hazard: Products may contain foreign objects (plastic).
January 15, 2025Food & BeverageFDA
HP Hood (VERNON) recalls WELLSLEY FARM VANILLA NON-FAT GREEK YOGURT; 40 oz; UPC 888670048078
Hazard: Products may contain foreign objects (plastic).
January 15, 2025Food & BeverageFDA
Dairyland Produce, LLC recalls Texas Harvest Product: 01035 Cucumber Sliced 5# 5-pound trays with sealed film
Hazard: Cucumbers have the potential to be contaminated with Salmonella.
January 15, 2025Food & BeverageFDA
C.H. Guenther & Son, Inc. recalls 235214 Baker's Source Traditional Cornbread Mix Complete, 5 LB Bags, 30 LB Cases Foodservice Use, Human Consumption & mi
Hazard: Undeclared egg allergen
January 15, 2025Food & BeverageFDA
Palermo Villa, Inc recalls Connie's Classic Thin Crust Cheese Pizza, Chicago's Finest. Net Wt 20.36 oz. (1lb 4.36 oz) 577g. UPC 0 75706-19104 8.
Hazard: Foreign material (plastic)
January 15, 2025Food & BeverageFDA
Better Brands Inc. recalls Chow Ciao Whole Grain Breaded Broccoli Nuggets - 30 lbs.
Hazard: Contains foreign object (metal)
January 15, 2025Food & BeverageFDA
Olympia Foods recalls Olympia Foods Grecian Dip Tzatziki sauce, item 100, 4 lb. tubs, UPC 10045059001001, 4 tubs per case; item 104, 32lbs pai
Hazard: potential for salmonella
January 15, 2025Food & BeverageFDA
Grecian Delight/Kronos recalls Nick The Greek Spicy Yogurt Pail, 42lbs pail, UPC 10075365177756, SKU SA000085
Hazard: potential for salmonella
January 15, 2025Food & BeverageFDA
Grecian Delight/Kronos recalls US Foods Chef's Line Greek Yogurt Tzatziki 4lbs tub, UPC 758108679962, SKU SAL519448, 2 tubs per case. Nick The Greek
Hazard: potential for salmonella
January 15, 2025Food & BeverageFDA
Grecian Delight/Kronos recalls Grecian Delight Tzatziki sauce, 3.75 lb. tub, UPC 07365000286, SKU SAL028, 4 tubs per case. Sysco Classic Tzatziki sauce
Hazard: potential for salmonella
January 15, 2025DrugsFDA
Granules Pharmaceuticals Inc. recalls Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg, 1000-count bottles, Rx Only, Manufactured by: Granules In
Hazard: Presence of Foreign Tablets/Capsules: A Paracetamol 500 mg tablet was found in a 1000-count bottle of Metformin HCL ER Tablets USP, 500 mg.
January 15, 2025DrugsFDA
Jubilant Draximage Inc., dba Jubilant Radiopharma recalls Kit for the Preparation of Technetium Tc 99m Sulfur Colloid Injection, 10 mL Multi-Dose Reaction Vial, 5 vial Box, Rx On
Hazard: Failed Stability Specifications
January 15, 2025DrugsFDA
Rising Pharma Holding, Inc. recalls Duloxetine DR Capsules USP 60 mg, a) 30 count (NDC 57237-019-30) and b) 1000 count (NDC 57237-019-99) bottles; Distribu
Hazard: CGMP Deviations; Presence of N-nitroso-duloxetine impurity above recommended interim limit.
January 15, 2025DrugsFDA
Rising Pharma Holding, Inc. recalls Duloxetine Delayed-Release Capsules USP 20 mg, 60 count bottles, Rx only, Distributed by: Rising Pharm Holdings, Inc., E
Hazard: CGMP Deviations; Presence of N-nitroso-duloxetine impurity above recommended interim limit.
January 15, 2025DrugsFDA
Rising Pharma Holding, Inc. recalls Duloxetine Delayed-Release Capsules USP 30 mg, a) 30 count (NDC 57237-018-30) and b) 1000 count (NDC 57237-018-99) bottl
Hazard: CGMP Deviations; Presence of N-nitroso-duloxetine impurity above recommended interim limit.
January 15, 2025DrugsFDA
Granules Pharmaceuticals Inc. recalls Colchicine Capsules 0.6 mg, 30-count bottles, Rx only, Manufactured by: Granules Pharmaceuticals Inc. Chantilly, VA 2015
Hazard: Failed Dissolution Specifications: Out of specification observed during the accelerated stability conditions for the 30 count bottles.
January 15, 2025DrugsFDA
Eugia US LLC recalls Progesterone Injection USP, 500mg per 10 mL (50mg/mL), 10 mL Multiple Dose Vial, Rx Only, Mfd. in India for: Eugia US LL
Hazard: Presence of Particulate Matter: A market complaint was received of a glass piece in the vial.