Search by meaning, not just keywords: describe the product or the hazard and we find matching recalls even when the official notice uses different words. Brand names and model numbers work too.
Latest recalls
35,025 found- Lower riskMedical device
Becton Dickinson & Co. recalls BioGX SARS-CoV-2 Reagents for BD MAX System Catalog number (REF) 444213. In vitro diagnostic. SARS-CoV-2 Reagents is a
Becton Dickinson recalls BioGX SARS-CoV-2 Reagents for BD MAX System (catalog 444213) due to mislabeled N1/N2 pouches. This could cause false negatives in SARS-CoV-2 tests, risking missed diagnoses and spread of COVID-19.
Becton DickinsonJan 7, 2021 - Use cautionMedical device
Baxter Healthcare Corporation recalls The PrisMax System Version II Hemodialysis Delivery System: Automatic Repositioning System Pump Assembly, specifically
Baxter Healthcare recalls PrisMax System Version II hemodialysis pumps with specific tubing models (955626, 955558, 955701) that may cause alarm situations during self-test and therapy, potentially interrupting treatment. The recall includes units with serial numbers listed in the record.
Baxter HealthcareJan 7, 2021 - Lower riskMedical device
Cardinal Health 200, LLC recalls Kendall Spill Kit, 6 Per Case, NonsterileI, BB6016K
Cardinal Health recalls Kendall Spill Kits with potentially rips or tears in gowns. Affected lots include 916197X through 931205X. Consumers should check their kits for damaged gowns.
Cardinal HealthJan 7, 2021 - Lower riskMedical device
Cardinal Health 200, LLC recalls Lab Coats SMS X-Large Blue, SKU 2203LC Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to
Cardinal Health recalls blue lab coats and isolation gowns with potential rips, holes, or tears that could compromise protection during medical use.
Cardinal HealthJan 7, 2021 - Use cautionDrug
American Health Packaging recalls Nitrofurantoin Capsules USP (Monohydrate/Macrocrystals), 100 mg, 100 per carton (10 capsules x 10 blister cards), Rx
American Health Packaging is recalling Nitrofurantoin Capsules USP 100 mg due to failed dissolution specifications. Check your lot number and expiration date.
American Health PackagingJan 7, 2021 - UnratedDrug
Bausch Health Companies, Inc. recalls Phytonadione Tablets 5mg, 30-count bottle, Rx Only, Manufactured For: Oceanside Pharmaceuticals, a division of Valeant
Bausch Health recalls 5mg Phytonadione tablets with potential impurity issues from stability testing. Affected lots may pose risks if used improperly.
Bausch HealthJan 7, 2021 - Lower riskFood
Western Mixers Produce & Nuts, Inc. recalls First Street Goody Goody Trail Mix 10 oz. (283g)S&F Item#52892 Unit UPC# 797565204201; First Street Goody Goody Trail
Recall of trail mix products containing undeclared tree nuts (cashews) due to allergen risk. Consumers should check product labels for lot numbers and contact manufacturer for details.
First Street Goody GoodyJan 7, 2021 - Lower riskFood
BLUE STONE IMPORT USA INC recalls SAMYANG Buldak Hot Chicken Flavor Sauce, Hot Chili Sauce, Net Wt.: 200g (7.05oz)
SAMYANG recalls 200g hot chicken and chili sauces due to undeclared wheat, egg, and milk. Consumers should check product labels for lot numbers and contact Blue Stone Import USA for details.
SAMYANGJan 7, 2021 - Stop using nowConsumer product
Noble House Home Furnishings Recalls Chests, Cabinets and Dressers Due to Tip-Over and Entrapment Hazards (Recall Alert)
Noble House recalls chests, cabinets, and dressers due to tip-over and entrapment hazards. Check your model numbers for a full refund.
Noble HouseJan 7, 2021 - Stop using nowConsumer product
John Deere Recalls Frontier Rotary Tillers Due to Injury Hazard (Recall Alert)
John Deere recalls Frontier rotary tillers due to missing safety signs on PTO drivelines. Stop using immediately and contact a dealer for free repair.
FrontierJan 7, 2021 - Lower riskMedical device
Baxter Healthcare Corporation recalls Infusion Pump
Baxter Healthcare recalls specific infusion pumps with battery codes 35083, 35162, 35195, 35724, 35223, and 36010 due to battery performance issues from prolonged storage.
Baxter HealthcareJan 6, 2021 - Lower riskMedical device
Arrow International Inc recalls Arrow AGB+ Multi-Lumen CVC Kit 7Fr 3 Lumen- Intended for venous access to the central circulation by the way of the
Arrow recalls AGB+ Multi-Lumen CVC Kits (CDC-45703-1A) due to potential allergic reactions in patients sensitive to chlorohexidine, silver sulfadiazine, or sulfa. Affected kits may have incorrect labeling.
ArrowJan 6, 2021 - Lower riskMedical device
Roche Diagnostics Operations, Inc. recalls 9180 Electrolyte Analyzer - Product Usage: intended to be used for the measurement of sodium, potassium, chloride,
Roche recalls 9180 Electrolyte Analyzer units with serial numbers listed in the record. The device may display calcium results with incorrect arrow direction, potentially leading to misinterpreted results and incorrect medical decisions.
RocheJan 6, 2021 - Use cautionMedical device
Respironics California, LLC recalls PHILIPS BATTERY, V60 14.4V, 11.0 Ah, 163 Wh, REF 1076374(1058272), LOT M94663-P1 - Product Usage: The ventilator is
Respironics recalls specific ventilator batteries due to unqualified design verification. Affected units may pose safety risks if used without proper certification.
RespironicsJan 6, 2021 - Lower riskDrug
DLC Laboratories, Inc recalls Sulfur Ointment 10%, Pomada de Azufre, 2.6 OZ (73.7g) jar; Manufactured by/ Fabricado por: De La Cruz Products, A
DLC Laboratories recalls Sulfur Ointment 10% jars with incorrect Camphor labeling. This mix-up may cause confusion about the product's active ingredients.
DLC LaboratoriesJan 6, 2021 - Lower riskFood
EVR FOODS INC recalls "LAVVA Blueberry Dairy Free Pili Nut Yogurt. NO SUGAR ADDED. NET WT 5.3OZ (150g) ***KEEP REFRIGERATED***DISTRIBUTED BY
EVR Foods recalls blueberry dairy-free yogurt that may contain mold. Consumers should check for mold and discard if found. Product sold with specific UPC codes.
EVR FOODS INCJan 6, 2021 - Stop using nowConsumer product
Rust-Oleum Recalls Aerosol Paint Due to Injury Hazard
Rust-Oleum recalls 20-oz Professional Bright Galvanizing Compound Spray due to risk of container detachment causing injury. Affected units have product number 7584838 and batch code H0304A. Consumers should stop using and return for refund.
Rust-OleumJan 6, 2021 - Stop using nowConsumer product
Massimo Motor Sports Recalls Percussion Massage Guns Due to Fire Hazard; Sold Exclusively at Costco
Massimo recalls all Percussion Massage Guns (model EM003) sold at Costco due to fire risk from overheating lithium-ion batteries. Consumers must stop using and get a refund.
MassimoJan 6, 2021 - Stop using nowConsumer product
Academy Sports + Outdoors Recalls Ozone 500 Density Bicycles Due to Fall and Injury Hazards
Academy Sports + Outdoors recalls Ozone 500 Density bicycles sold Oct-Nov 2020. Stop using immediately due to fall risk from loose front wheel hardware.
OzoneJan 6, 2021 - Use cautionMedical device
Hamilton Medical AG recalls HAMILTON-H900 Humidifier, Models: 950001, 950004
Hamilton Medical recalls H900 humidifiers (models 950001, 950004) with software 1.10c due to delayed low water alarm when chamber is empty, risking undetected water absence during medical ventilation.
Hamilton MedicalJan 5, 2021 - Lower riskMedical device
Helena Laboratories, Corp. recalls Cascade Abrazo aPTT Test Card - Product Usage: are to be used with the Cascade Abrazo analyzer and are intended for the
Helena Laboratories recalls Cascade Abrazo aPTT Test Cards (Model 5722) due to intermittent shorter clot times. Affected lots expire by Dec 2021. Contact for replacement.
Helena LaboratoriesJan 5, 2021 - Lower riskMedical device
Biomeme, Inc. recalls Nucleic acid-based in vitro diagnostic devices for the detection of 2019-novel coronavirus (2019-nCoV) and/or diagnosis
Biomeme recalls certain coronavirus test devices that may fail due to a software error causing incomplete testing. Affected units include Franklin Real-Time PCR Thermocyclers with specific model numbers and software version 6.4.3.
BiomemeJan 5, 2021 - Lower riskFood
Dole Fresh Vegetables Inc recalls Dole Chopped Kit Sesame Asian Salad & Topping Net Wt: 9.5 oz (269 g) Dressing Net: 2.5 FL oz (72 mL) Total Net Wt.
Dole recalls sesame Asian salad dressing due to undeclared egg allergen in some packages. Affected lots B364016 and B364017 from 2021-01-15 best by date. Consumers should check labels for these codes.
DoleJan 5, 2021 - Lower riskFood
Weis Markets, Inc., Ice Cream Division recalls Klein s Cookies and Cream Bulk Packaged in a 3 gallon paper drum.
Weis Markets recalls Klein's Cookies and Cream bulk ice cream in 3-gallon paper drums after metal contamination found. Consumers should check for metal fragments in the product.
Weis MarketsJan 5, 2021 - Use cautionVehicle
MERCEDES-BENZ AMG C43 (2021) recall — Seats
Mercedes-Benz recalls 2021 C43 models with faulty seat position switches that may prevent airbags and seat belts from deploying properly in crashes. Owners must contact MBUSA for free replacement.
Mercedes-BenzJan 4, 2021 - Use cautionVehicle
MERCEDES-BENZ AMG GLB35 (2021) recall — Structure
Mercedes-Benz recalls 2021 GLB35 AMG vehicles with potentially detachable side spoilers that could cause crashes. Owners must have spoilers inspected or replaced free by dealers.
Mercedes-BenzJan 4, 2021 - Use cautionVehicle
INTERNATIONAL LT (2021) recall — Parking Brake
Navistar recalls 2021 International LT trucks with potential air leak in parking brake causing crash risk. Owners notified via mail; free repairs available.
NavistarJan 4, 2021 - Use cautionVehicle
INTERNATIONAL MV (2021) recall — Service Brakes, Air
Navistar recalls 2021 International trucks with Bendix pressure switches due to potential brake failure. Owners must have SC-3 check valves replaced free by dealers.
NavistarJan 4, 2021 - Use cautionVehicle
MACK ANTHEM (AN) (2020) recall — Electronic Stability Control (Esc)
Mack is recalling 2018-2022 Anthem trucks with camelback suspension that may drift out of lane, risking crashes. Owners must contact Mack for free reprogramming by April 21, 2021.
MackJan 4, 2021 - Use cautionMedical device
Cook Inc. recalls Cook Medical Kwart Retro-Inject Ureteral Stent Set 7.0Fr. 22-32cm -Used for retrograde injection during Extracorporeal
Cook Medical recalls ureteral stent sets with incorrect material that may break during use. Affected models include 7.0Fr. 22-32cm for ESWL procedures. Contact for return or replacement.
CookJan 4, 2021
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