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
34,956 found- Use cautionVehicle
BUICK REGAL (2018) recall — Seat Belts
General Motors recalls 2018 Buick Regal vehicles with improperly routed rear seat belts that may not restrain passengers effectively during crashes. Owners should contact GM for free repairs.
BuickDec 4, 2018 - Use cautionVehicle
FOREST RIVER GEORGETOWN (2019) recall — Structure
Forest River recalls 2018-2019 Georgetown RVs due to risk of entry door opening unexpectedly while moving, potentially causing injury. Owners must contact dealer for free door frame repairs.
Forest RiverDec 4, 2018 - Lower riskMedical device
Intuitive Surgical, Inc. recalls Da Vinci Xi/X EndoWrist Monopolar Curved scissors (MCS), model number 470179-19, UDI: (00) 886874112298
Intuitive Surgical recalls Da Vinci Xi/X EndoWrist Monopolar Curved scissors (model 470179-19) due to potential failure to recognize monopolar energy in electrosurgical units, which could prevent proper surgical function.
Intuitive SurgicalDec 4, 2018 - Lower riskMedical device
Stryker Instruments Div. of Stryker Corporation recalls Triton Sponge System (Software), GAUS-3, Software Versions 4.6.5, 4.8.7, 4.9.6
Stryker recalls Triton Sponge System software versions 4.6.5, 4.8.7, and 4.9.6 for updated instructions on sponge handling and calibration placards.
StrykerDec 4, 2018 - Lower riskMedical device
Waldemar Link GmbH & Co. KG (Mfg Site) recalls BiMobile UHMWPE Liner: ID-28mm/OD-54mm, Reference Number 184-260/04 The LINK BiMobile Dual Mobility System is indicated
Waldemar Link recalls BiMobile UHMWPE Liner (ID-28mm/OD-54mm, Ref 184-260/04) due to potential incorrect part numbers in labeling that could lead to patient record errors. Affected patients should contact the manufacturer for guidance.
Waldemar LinkDec 4, 2018 - UnratedMedical device
Elekta, Inc. recalls MOSAIQ Oncology Information System Version 2.64. MOSAIQ is an oncology information system used to manage workflows for
Elekta recalls MOSAIQ Oncology Information System Version 2.64 due to potential incorrect isocenter settings when copying treatment fields, which could affect radiation therapy accuracy.
ElektaDec 4, 2018 - Use cautionMedical device
Agfa-Gevaert, N.V. recalls DX-D 600 DIRECT RADIOGRAPHY SYSTEM Product Usage: The DX-D 600 system is a ceiling mounted General Radiography X-Ray
Agfa recalls specific DX-D 600 X-Ray systems due to potential continued movement after button release during use, posing a risk of injury to patients or staff.
AgfaDec 4, 2018 - Lower riskMedical device
Randox Laboratories Ltd. recalls Randox CALCIUM (Ca) Colorimetric Method RX Series Cat. No. CA 3871, R1. Arsenazo Reagent 9 x 51ml GTIN: 05055273200904
Randox recalls calcium reagents that may cause false high or low test results. Affected products include specific lot codes of the Randox Calcium Colorimetric Method RX Series.
RandoxDec 4, 2018 - Lower riskDrug
Epic Pharma, LLC recalls Estradiol Tablets, USP, 2 mg, 100-count bottle, Rx Only, Distributed by: Epic Pharma, LLC Laurelton, NY 11413, NDC
Epic Pharma recalls 100-count Estradiol 2 mg tablets due to a foreign tablet found in some bottles. This is a safety issue for patients using prescription hormone therapy.
Epic PharmaDec 4, 2018 - UnratedDrug
Mylan Laboratories Limited, (Nashik FDF) recalls Valsartan and Hydrochlorothiazide Tablets, USP 320/25 mg, (a) 90-count bottle (NDC 0378-6325-77), (b) 500-count bottles
Mylan recalls 90-count and 500-count Valsartan/Hydrochlorothiazide tablets (320/25 mg) made in India with trace NDEA impurity. FDA confirmed impurity in API; no specific remedy stated.
MylanDec 4, 2018 - Lower riskFood
Root 23 LLC recalls ROOT 23 CUCUMBER HABANERO SIMPLE SYRUP 375 ml
Root 23 recalls cucumber habanero syrup due to unrecorded temperature during processing. Consumers should check product code 070320 for affected items.
Root 23Dec 4, 2018 - Lower riskFood
Ellgof Inc. recalls HomeFresh FOODS Suya Barbecue Seasoning, UPC: 6 033000120298, Net Wt: 240g/0.53 lbs; Produced in Ghana by: ELSSY KESS
HomeFresh Suya Barbecue Seasoning (UPC 6033000120298) contains undeclared peanuts. Consumers should check labels and avoid if allergic to peanuts.
HomeFresh FOODSDec 4, 2018 - Stop using nowFood
Earthworks Health recalls Diatomaceous Earth packaged in the following ways: 1) Perma-Guard, Fossil Shell Flour, Anti-caking agent, Food Chemical
Earthworks Health recalls diatomaceous earth products containing elevated lead, arsenic, and chromium. Consumers should stop using these items due to potential health risks from harmful metals.
Earthworks HealthDec 4, 2018 - UnratedFood
Bauer's Candies, Inc. recalls 1 lb QVC combo, 1 lb combo, 2 lb combo, 12 oz combo, 8 oz combo, holiday combo
Bauer's Candies recalls several holiday candy combos due to potential Hepatitis A exposure. Consumers should check product labels for affected items.
Bauer's CandiesDec 4, 2018 - Stop using nowConsumer product
Signature Hardware Recalls Wall-Mounted Shower Seats Due to Fall and Laceration Hazards
Signature Hardware recalls wall-mounted shower seats due to corroding aluminum hardware. Stop using immediately for a full refund.
Signature HardwareDec 4, 2018 - Stop using nowConsumer product
Foremost Recalls Shower Doors and Panels Due to Injury and Impact Hazards (Recall Alert)
Foremost recalls glass shower doors and panels with faulty pivot hinges that can separate, causing injury. Affected models include Cove and Suave series. Consumers must stop using and get free replacements.
ForemostDec 4, 2018 - Use cautionVehicle
FORD FOCUS (2016) recall — Power Train
Ford is recalling 2015-2016 Focus vehicles with 1.0L GTDI and 6-speed manual transmission due to potential transmission fluid leaks near ignition sources that could cause fire. Owners must contact Ford for free clutch repairs.
FordDec 3, 2018 - Use cautionVehicle
FCCC XCR (2016) recall — Steering
DTNA recalls 2011-2017 FCCXCR trucks with faulty power steering hose that may cause fire from electrical arcing due to leaking fluid. Owners must have hose rerouted by dealers.
DTNADec 3, 2018 - Use cautionVehicle
FORD FUSION (2018) recall — Steering
Ford is recalling certain 2018 Fusion vehicles due to a steering wheel detachment risk. Owners must contact Ford for a free bolt replacement to prevent loss of steering control.
FordDec 3, 2018 - Use cautionMedical device
Philips Medical Systems Nederlands recalls Ingenia Elition S, Ingenia Elition X
Philips recalls Ingenia Elition S and X models with software R5.5.0 due to potential table movement restart during manual button presses. Affected units have specific serial numbers listed.
Philips Medical SystemsDec 3, 2018 - Use cautionMedical device
PENTAX of America Inc recalls C2 CryoBalloon Controller, REF: FG-1017, with Controller Software v1.18.258 The C2 CryoBalloon Ablation System is
Pentax recalls C2 CryoBalloon Controller software v1.18.258 due to potential balloon overpressure during nitrous oxide use, risking tissue injury. Affected units sold with specific reference numbers.
PentaxDec 3, 2018 - Lower riskMedical device
Randox Laboratories Ltd. recalls Fructosamine Control 3, FR2996 This product is intended for in vitro use in the calibration of the Randox Liquid
Randox recalls Fructos: 25% value decrease in calibration controls may affect test accuracy. Affected units: 500FR model for in vitro use.
RandoxDec 3, 2018 - Lower riskMedical device
PENTAX of America Inc recalls Pentax Medical C2 CryoBalloon Standard Focal Catheter, Model FG 1028, Sterile, RX. Product Usage: The C2 CryoBalloon
Pentax recalls specific models of cryosurgical catheters due to potential incorrect dose transmission to the controller, which could affect treatment safety. Affected units include certain lot numbers from 2018.
PentaxDec 3, 2018 - Lower riskMedical device
Conformis, Inc. recalls iTotal CR Total Knee Replacement System, TCR-121-1111 (Catalog No.) / TCR-121-1111-010102 (Model No.) M5725INT0600010
Conformis recalls iTotal CR Total Knee Replacement Systems with incorrect patient ID labels and components. This could lead to wrong patient matches during surgery. Affected units have specific model numbers and serial numbers.
ConformisDec 3, 2018 - Lower riskFood
Hiland Dairy Foods Company LLC recalls Hiland Chocolate Milk, 1/2 gallon (1.89 L). Hiland Dairy Springfield, MO 65803
Hiland Dairy recalls chocolate milk products due to egg nog flavor complaints from same plant. Products may contain undeclared egg ingredients.
HilandDec 3, 2018 - Use cautionVehicle
FORD ESCAPE (2018) recall — Service Brakes, Hydraulic
Ford is recalling 2018 Escape vehicles with potentially faulty brake hoses that could leak brake fluid, increasing stopping distance and crash risk. Owners should contact Ford for free brake hose replacement.
FordDec 2, 2018 - Use cautionVehicle
JAGUAR F-PACE (2018) recall — Electrical System
Jaguar recalls 2017-2018 F-Pace vehicles with potential blank instrument cluster causing speed information loss. Owners must contact Jaguar for free software update.
JaguarDec 1, 2018 - Use cautionVehicle
COACHMEN VIKING (2018) recall — Equipment
Forest River is recalling 2018 Coachmen Viking trailers with a Smart-Jack power tongue jack that may crack, causing unintended movement and crash risk. Owners must contact Forest River or Lippert for free replacement.
Forest RiverDec 1, 2018 - Lower riskMedical device
Canadian Hospital Specialties recalls MED-RX POLYURETHANE FEEDING TUBE For Pediatric Use with Orange Radioplaque Stripe and Enteral Connector, 6.5Fr X 24"
Canadian Hospital Specialties recalls pediatric feeding tubes with possible incorrect size (5FR instead of 6.5FR) that could cause improper feeding. Affected units may need verification.
Canadian Hospital SpecialtiesDec 1, 2018 - Use cautionVehicle
DUCATI PANIGALE V4 (2018) recall — Engine And Engine Cooling
Ducati is recalling 2018-2019 Panigale V4 motorcycles due to timing chain tensioner oil leaks that could increase crash risk. Owners must contact dealers for free bolt tightening.
DucatiNov 30, 2018
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