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
35,004 found- Use cautionMedical device
Philips North America, LLC recalls Philips Sterilizable Defibrillator Internal Paddles - Internal paddles are an accessory to the compatible
Philips recalls sterilizable defibrillator internal paddles that may wear out and fail to deliver therapy during cardiac emergencies. Users must follow operational checks to ensure safety.
PhilipsApr 20, 2020 - Lower riskMedical device
Suntech Medical, Inc. recalls Oscar 2, Model 250 System
Suntech Medical recalls Oscar 2 Model 250 blood pressure monitors that may display incorrect decimal points when readings are three-digit numbers in mmHg. Affected units have specific serial numbers.
Suntech MedicalApr 20, 2020 - Lower riskMedical device
Cardinal Health Inc. recalls Professional Urine Drug Control, Item code 88010 - Product Usage: The Alere Professional Cup Urine Drug Controls are
Cardinal Health recalls Alere Professional Urine Drug Controls with improper refrigeration causing misdiagnosis. Affected units may lead to incorrect test results if stored outside approved temperatures.
AlereApr 20, 2020 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Siemens Cios Alpha VA30-mobile X-Ray system, Material # 11105200 The Cios Alpha and Cios Spin are a mobile X-Ray system
Siemens recalls Cios Alpha VA30 mobile X-Ray systems with serial numbers 40057-40135 due to risk of electrical shock if main cable unplugged during use. The error message Err 16305/80 indicates unsafe voltage at X10 connector.
SiemensApr 20, 2020 - Lower riskMedical device
Trividia Health, Inc. recalls TRUE METRIX SELF MONITORING BLOOD GLUCOSE SYSTEM - Product Usage: is intended for the quantitative measurement of
Trividia Health recalls a blood glucose meter that displays results in mmol/L instead of mg/dL, causing incorrect readings for diabetes management.
Trividia HealthApr 20, 2020 - Lower riskDrug
Lupin Pharmaceuticals Inc. recalls Lisinopril Tablets USP, 20 mg, 1000-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore MD
Lupin Pharmaceuticals recalls 20mg Lisinopril tablets due to potential mix-up with 10mg tablets in sealed bottles. Affected products have NDC 68180-0981-03 and lot # Q000255.
Lupin PharmaceuticalsApr 20, 2020 - Lower riskDrug
Glaxosmithkline Consumer Healthcare Holdings recalls ChapStick Total Hydration Moisture + Tint + SPF15 Very Berry Net Wt. 0.08 OZ (2.2g) Marketed by: Pfizer, Madison, NJ
Glaxosmithkline recalls ChapStick Total Hydration Moisture + Tint + SPF15 Very Berry (0.08 oz) due to potential separation in packaging. Affected units have specific NDC and lot numbers. Consumers should check labels and contact Pfizer for details.
GlaxosmithklineApr 20, 2020 - Stop using nowDrug
Fresenius Kabi USA, LLC recalls Ketorolac Tromethamine Injection, USP, 30 mg per mL, packaged in 1 mL Single Dose Vials (NDC 63323-162-00); 25 x 1 mL
Fresenius Kabi recalls over 5 million vials of Ketorolac Tromethamine Injection due to particulate matter. Check lot numbers and expiration dates for affected units.
Fresenius KabiApr 20, 2020 - Lower riskFood
Ocean Spray Cranberries Inc. recalls 5.5 oz cans of Ocean Spray Pink Lite Cranberry Juice Drink
Ocean Spray recalls 5.5 oz Pink Lite Cranberry Juice Drink cans with undeclared sulfites. Consumers should check UPCs and stop using if purchased before January 24, 2021.
Ocean SprayApr 20, 2020 - Lower riskFood
La Sonorense, Inc. recalls 12", 10" Pressed Wheat Flour Tortillas, packaged in quantities of 1-2 dozen per package. Each package is twist-tied and
La Sonorense recalls 12" and 10" pressed wheat flour tortillas sold in 1-2 dozen packages from March 16, 2020 onward. The product contains undeclared wheat and fails to list all ingredients, posing a risk for those with wheat allergies.
La SonorenseApr 20, 2020 - Lower riskDrug
B. Braun Medical Inc recalls Ceftazidime for Injection USP and Dextrose for Injection USP, 2 g, 50 mL Duplex Container, RX only, B Braun Medical
B. Braun Medical recalls Ceftazidime for Injection USP and Dextrose for Injection USP, 2g/50mL, due to stability problems that could affect safety.
B. Braun MedicalApr 18, 2020 - Lower riskFood
Mellace Family Brands California Inc recalls Wegmans brand Semi-Sweet Chocolate Nonpareils in an 18.5 oz. (524 g) plastic container, 12 plastic containers per case.
Wegmans recalls 12-pack of 18.5 oz semi-sweet chocolate nonpareils due to potential undeclared milk allergen. Consumers should check lot numbers 98581 and 05033.
WegmansApr 18, 2020 - Use cautionVehicle
FOREST RIVER FLAGSTAFF (2016) recall — Tires
Forest River is recalling 2016 Rockwood RLT2604WS, WRLT2604WS, Flagstaff FLT26RLWS and WFLT26RLWS trailers due to front tire damage from slide out bracket contact. Free lift kit installation and tire replacement offered.
Forest RiverApr 17, 2020 - Use cautionVehicle
INTERNATIONAL HV (2020) recall — Fuel System, Diesel
Navistar recalls 2017-2021 International trucks with Cummins B6.7 diesel engines and specific fuel module options due to fire risk from overheating fuel heaters.
NavistarApr 17, 2020 - Use cautionVehicle
IC BUS CESB (2020) recall — Fuel System, Diesel
Navistar is recalling certain 2017-2021 school buses with Cummins diesel engines due to a fire risk from overheating fuel heaters. Owners must contact Cummins for free repairs to prevent potential fires and engine stalls.
NavistarApr 17, 2020 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Cios Spin Image-Intensified Fluoroscopic X-Ray System, Model Numbers VA30-10308194
Siemens recalls Cios Spin Image-Intensified Fluoroscopic X-Ray Systems with model VA30-10308194 due to risk of electrical shock from unplugged cables. Affected units may have unsafe voltage at X10 connector.
SiemensApr 17, 2020 - Lower riskMedical device
Alcon Research LLC recalls Acrysof, IQ IOL w/UltraSert System, AcrySof IQ ASPHERIC IOL, 20.5 D, SP ACRYLIC FOLDABLE LENS, w/UltraSert DELIVERY
Alcon recalls Acrysof IQ IOLs with incorrect diopter settings that may cause vision issues. Affected models include 20.5 D SP ACRYLIC FOLDABLE LENS with UltraSert delivery system. Contact Alcon for details.
AlconApr 17, 2020 - UnratedMedical device
Biomet, Inc. recalls Knee Products: 154335 Oxford Partial Knee System, Fixed Lateral Tibial Construct, Left, Cemented, D3 154336 Oxford
Biomet recalls specific knee replacement models due to potential elevated endotoxin levels exceeding safety limits. Affected products include Oxford Partial Knee Systems with certain model numbers and lot codes. Consumers should contact Biomet for details.
BiometApr 17, 2020 - Use cautionMedical device
Baxter Healthcare Corporation recalls Gambro Cartridge Low Weight-Low Volume Blood Transport System for Hemodialysis Blood Set - Product Usage: is intended
Baxter recalls specific hemodialysis blood transport systems due to potential tubing disconnection during use. Affected units have unique product codes and lot numbers. Stop using immediately to prevent complications.
BaxterApr 17, 2020 - Lower riskFood
Freedman Food Service, Inc dba Buckhead Meat & Seafood of Houston recalls 7075931 Flounder Stuffed W/ Seafood FRZN, Net Wt LBS 15.00 (6.80 KG), 20 packages per case
Buckhead Meat & Seafood recalls 20-pack frozen flounder stuffed with seafood due to potential undeclared milk (whey) in ingredients. Consumers should check package dates and contact for details.
Buckhead Meat & SeafoodApr 17, 2020 - Use cautionVehicle
SUBARU ASCENT (2019) recall — Fuel System, Gasoline
Subaru recalls 2019 Ascent vehicles with faulty fuel pump that may cause engine stalling without restart, increasing crash risk. Free replacement pump available.
SubaruApr 16, 2020 - Use cautionVehicle
FORD EXPEDITION (2020) recall — Seat Belts
Ford is recalling 2020 Expedition vehicles with faulty front passenger seatbelt buckles that may misclassify occupants during crashes, increasing injury risk. Owners must get free replacement buckles.
FordApr 16, 2020 - Lower riskMedical device
Elekta Inc recalls Elekta MONACO RTP Sytem, radiation treatment planning software system - Product Usage: The Monaco system is used to
Elekta recalls Monaco RTP radiation treatment software version 5.40.00 and 5.40.01 due to potential inaccurate radiation dose delivery. Affected users should contact Elekta for details.
ElektaApr 16, 2020 - Lower riskMedical device
Becton Dickinson & Company recalls BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535
Becton Dickinson recalls BD Posiflush SF Saline Flush Syringes with packaging holes that could compromise sterility. Affected units include specific lots sold in the US. Consumers should check their syringe packaging for holes and contact BD for details.
Becton DickinsonApr 16, 2020 - Lower riskMedical device
Howmedica Osteonics Corp. recalls Stryker Orthopaedics-Restoration Anatomic Hemispherical Shell, Size 54 Right, Sterile, Catalog # 504-02-54C-R, UDI
Howmedica recalls Stryker Restoration Anatomic Hemispherical Shell Size 54 Right. The device may fall off its post in packaging, causing debris to loosen. Consumers should check product details and contact Howmedica for guidance.
HowmedicaApr 16, 2020 - Lower riskFood
Whole Foods Market recalls Whole Foods Market Queso Sauce PLU code printed on the product scale labels beginning with 74135 sold in clear plastic
Whole Foods Market recalls quesosauce with PLU code 74135 due to potential cashew contamination. Consumers should check product labels for the specific code and avoid use if concerned.
Whole Foods MarketApr 16, 2020 - Use cautionConsumer product
Wyndmere Naturals Recalls Birch Sweet Essential Oil and Aches & Pains Synergistic Essential Oil Blend Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning
Wyndmere recalls Birch Sweet and Aches & Pains Essential Oils due to non-child-resistant packaging, risking poisoning if young children swallow. Consumers should store safely and get a refund or replacement cap.
WyndmereApr 16, 2020 - Use cautionConsumer product
The Vitamin Shoppe Recalls Energy Formula Multivitamins Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
The Vitamin Shoppe recalls Energy Formula multivitamins due to non-child-resistant packaging, risking poisoning if young children swallow. Consumers should store out of reach and contact for disposal/refund.
The Vitamin ShoppeApr 16, 2020 - Use cautionConsumer product
Polaris Recalls PRO XD and Ranger Utility Vehicles Due to Injury Hazard (Recall Alert)
Polaris recalls 2019 PRO XD and 2020 Ranger UTVs due to potential seat belt failure during collisions or tip-overs. Owners must stop using and get free repairs.
PolarisApr 16, 2020 - Stop using nowConsumer product
Polaris Recalls Model Year 2019 to 2020 Ranger XP 1000 Off-Road Vehicles Due to Fire Hazard (Recall Alert)
Polaris recalls 2019-2020 Ranger XP 1000 & CREW XP 1000 off-road vehicles due to fire risk from misrouted fuel lines. Affected owners must stop using and contact a dealer for free repair.
PolarisApr 16, 2020
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83,592 recalls tracked · 72,039 explained in plain English · 10,976 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.