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
34,960 found- Lower riskMedical device
Cardiocommand Inc. recalls TAPSYSTEM Model 2A, REF 8002A
Cardiocommand recalls TAPSYSTEM Model : 2A units with specific serial numbers due to potential battery wire connection error affecting power switch.
CardiocommandJun 24, 2019 - Lower riskMedical device
Randox Laboratories, Limited recalls RX Daytona, Model Nos. RX4040 and RX4041
Randox recalls RX Daytona models RX4040 and RX404: Risk of internal wire melting and scorch damage due to sensor malfunction. Affected units have specific serial numbers.
RandoxJun 24, 2019 - Lower riskMedical device
Elekta, Inc. recalls Elekta Unity, Image-Guided Radiation Therapy System Elekta Unity using Magnetic Resonance Imaging is indicated for
Elekta recalls Unity radiation therapy systems due to QA software not displaying MR to MV offset values, risking treatment errors. Affected units include specific model numbers and installation dates.
ElektaJun 24, 2019 - Lower riskMedical device
OriGen Biomedical, Inc. recalls 3/8" FloPump, 32mL, (Sterile), REF 6400S, UDI: (01) 081432102013 1, Sterile EO, Rx Only
OriGen Biomedical recalls expired 3/8" FloPump pumps. These sterile medical devices may not be safe for use after expiration. Consumers should check product lot numbers and contact the company for details.
OriGen BiomedicalJun 24, 2019 - Lower riskMedical device
Fenwal Inc recalls Vigilant Agilia, Vigilant Drug'Lib, REF Z073476, versions 1.0 and 1.1 Product Usage: Vigilant Drug Lib is Dose Error
Fenwal recalls Vigilant Drug Lib software versions 1.0 and 1.1 due to potential dose errors in patient medication administration. This software works with Volumat MC Agilia infusion pumps to reduce errors but requires specific patient weight ranges.
FenwalJun 24, 2019 - UnratedMedical device
Centurion Medical Products Corporation recalls NOSEBLEED TRAY Kit Code: MNS3885
Centurion Medical recalls nosebleed tray kits containing nasal decongestant spray due to potential safety risks. Affected kits have specific lot numbers and expiration dates.
Centurion MedicalJun 24, 2019 - Lower riskMedical device
Philips Medical Systems (Cleveland) Inc recalls Ingenuity Core128 Model # 728323, computed tomography x-ray system
Philips recalls specific models of Ingenuity Core128 CT scanners due to potential image labeling errors during cardiac scans. Affected units may show incorrect phase tolerance settings, requiring immediate action to prevent misdiagnosis.
Philips Medical SystemsJun 24, 2019 - UnratedDrug
H J Harkins Company Inc dba Pharma Pac recalls Acetaminophen Children's Liquid, 160 mg/5 mL, 4 oz bottle, Manufactured by Torrent Pharma, Inc., Levittown, PA 19057,
Pharma Pac recalls acetaminophen children's liquid due to potential contamination with Burkholderia cepacia and Ralstonia pickettii bacteria. Affected lots manufactured in Levittown, PA. Consumers should contact the company for details.
Pharma PacJun 24, 2019 - Use cautionFood
Commercial Creamery Company of Idaho, Inc. recalls White Cheddar 5906-KD is a non-GMO White Cheddar Cheese Blend dried cheese powder. Product was shipped in bulk bags,
Commercial Creamery Company of Idaho recalls White Cheddar 5906-KD dried cheese powder due to potential Salmonella contamination. Consumers should avoid using this product to prevent foodborne illness.
Commercial CreameryJun 24, 2019 - Use cautionVehicle
FOREST RIVER GEORGETOWN (2020) recall — Equipment
Forest River recalls 2019-2020 Georgetown and FR3 motorhomes with slim-rack slideouts that may move unexpectedly, risking injury. Owners get free controller and switch updates.
Forest RiverJun 21, 2019 - Use cautionVehicle
COACHMEN CHAPARRAL LITE (2020) recall — Electrical System
Forest River recalls 2017-2020 Coachmen Chapparal Lite trailers with non-GFCI kitchen outlets. Unprotected outlets may cause electric shock, injury or death. Owners must replace with GFCI outlets by July 31, 2019.
Forest RiverJun 21, 2019 - Lower riskMedical device
Alto Development Corp recalls A&E Medical Corp. Ultra-Flex MYO/Wire Ultra-Flex Monopolar Pacing Wire Looped Electrode (M-21 SERIES)- Temporary Pacing
Alto Development Corp recalls Ultra-Flex Monopolar Pacing Wire (M-21 Series) due to updated instructions for use consistency between electrode IFU and instructions. This temporary cardiac pacing electrode may cause confusion in medical use.
Alto Development CorpJun 21, 2019 - UnratedDrug
Pharma-Natural Inc. recalls GENCONTUSS (Chlorpheniramine Maleate, 2mg; Dextromethorphan HBr, 10 mg; Phenylephrine HCl, 5 mg) in each 5 mL tsp,
Pharma-Natural Inc. recalls GENCONTUSS cough syrup due to manufacturing process failures. Products may not be safe as they were made without proper quality checks. Consumers should check their bottles for the NDC number 52083-650-16.
Pharma-NaturalJun 21, 2019 - Stop using nowConsumer product
Ranee's Recalls Women's Beach Cover-ups Due to Violation of Federal Flammability Standard
Ranee's tan and cream women's beach cover-ups fail flammability standards, risking burns. Consumers must stop using and get refunds.
Ranee'sJun 21, 2019 - Stop using nowConsumer product
Honeywell Recalls Gamewell-FCI and Notifier Photoelectric Smoke Sensors Sold with Fire Alarm Systems Due to Failure to Alert of a Fire
Honeywell recalls Gamewell-FCI and Notifier photoelectric smoke sensors due to malfunction risk. Contact manufacturer for free replacement.
HoneywellJun 21, 2019 - Stop using nowConsumer product
H.E. Industrial Recalls Electric Garage Heaters Due to Fire Hazard
H.E. Industrial recalls Profusion Heat electric garage heaters (model HA22-48M) due to fire hazard from overheating heating elements. Consumers must stop using and get refunds or gift certificates.
H.E. IndustrialJun 21, 2019 - Stop using nowMeat & poultry
C&S Wholesale Grocers Recalls Meat and Poultry Products due to Possible Temperature Abuse During Transport at Two Stores in New York
C&S Wholesale Grocers recalls meat and poultry sold at two New York Target stores on June 17, 2019, due to possible temperature abuse during transport.
C&S Wholesale GrocersJun 20, 2019 - Lower riskMedical device
Cincinnati Sub-Zero Products LLC, a Gentherm Company recalls Norm-O-Temp model 111Z
Cincinnati Sub-Zero Products recalls Norm-O-Temp 111Z devices that may cause tissue damage if overheated beyond 40°C for extended periods. Affected units have specific serial numbers and part numbers.
Sub-ZeroJun 20, 2019 - Lower riskMedical device
Siemens Medical Solutions USA, Inc recalls Cios care fusion system
Siemens recalls Cios Care Fusion System with material #10308192 and serial #31375 due to potential missing insulating foil in DAP chamber.
SiemensJun 20, 2019 - UnratedMedical device
St Jude Medical Inc. recalls ELLIPSE VR, REF: CD1377-36QC Implantable cardioverter defibrillators (ICDs)
St Jude Medical recalls ELLIPSE VR implantable cardioverter defibrillators with damaged aluminum wires that may cause electrical failures. No verification method available for vulnerable devices.
St Jude MedicalJun 20, 2019 - UnratedDrug
Macleods Pharma Usa Inc recalls Losartan Potassium Tablets 50 mg 1000 Tablets, USP Rx Only Manufactured for: Macleods Pharma USA inc. Plainsboro, NJ
Macleods Pharma USA recalls 50mg Losartan Potassium Tablets due to impurity detected in active ingredient. Prescription-only medication with NDC 33342-045-44 manufactured Nov 2019.
MacleodsJun 20, 2019 - Lower riskFood
Woolery Enterprises Inc. dba Will's Fresh Foods recalls Will's Fresh Foods Macaroni Salad, All Natural; A true Classic salad made astonishingly delicious - semolina pasta,
Will's Fresh Foods recalls macaroni salad due to wheat not being listed as an allergen. This poses a risk for people with wheat allergies.
Will's Fresh FoodsJun 20, 2019 - Stop using nowFood
Perrigo Company PLC recalls Parent's Choice Advantage Infant Formula Milk-Based Powder with Iron, 35 oz, 922 g, with UPC: 078742022468
Perrigo recalls Parent's Choice Advantage Infant Formula with possible metal fragments. Consumers should check UPC 078742022468 and lot code C26EVFV (use by Feb 26, 2021) for affected products.
PerrigoJun 20, 2019 - Lower riskFood
Tropical Nut & Fruit Company recalls Truly Good Foods Edamame Beans Roasted and Salted 7 oz. (198g) plastic clam shell DISTRIBUTED BY TRULY GOOD FOODS,
Tropical Nut & Fruit Company recalls roasted salted edamame beans due to missing allergen label on packaging. Consumers should check for missing contain statement on label.
Tropical Nut & Fruit CompanyJun 20, 2019 - Stop using nowConsumer product
Hunter Fan Recalls Brunswick Three and Four Light Ceiling Fans Due to Shock Hazard
Hunter recalls Brunswick three and four light ceiling fans with model numbers 52262-54185 due to electric shock risk from damaged light kit wires. Consumers must stop using and get a free replacement kit.
HunterJun 20, 2019 - Use cautionVehicle
BMW M3 (2012) recall — Electrical System
BMW is recalling certain 2008-2012 M3 models due to potential electrical power loss causing stalling and increased crash risk. Owners must have the battery cable connector replaced at no cost by dealers.
BMWJun 19, 2019 - Use cautionVehicle
AUDI A3 SPORTBACK E-TRON (2018) recall — Air Bags
Audi is recalling 2018 A3 Sportback E-TRON models with deactivated passenger air bags that may increase crash injury risk. Owners must contact dealers for free repairs.
AudiJun 19, 2019 - Use cautionVehicle
BLUE BIRD ALL AMERICAN (2019) recall — Electrical System
Blue Bird is recalling 2018-2019 school buses with PowerDrive 7000 EV electric drivetrains due to potential loss of power steering and drive, increasing crash risk. Owners must update VCU software for safety.
Blue BirdJun 19, 2019 - Stop using nowVehicle
AUDI Q5 (2019) recall — Air Bags
Audi is recalling certain 2019 Q5 vehicles due to a faulty passenger frontal air bag that may not deploy correctly. Check if your vehicle is affected.
AudiJun 19, 2019 - Lower riskMedical device
Elekta, Inc. recalls iGUIDE System with software build iGuide 2.2.0, 2.2.1, and 2.2.2
Elekta recalls iGUIDE System software versions 2.2.0-2.2.2 due to potential incorrect 3D position monitoring. Affected units have specific GTIN numbers and were sold with these software builds.
ElektaJun 19, 2019
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