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- Lower riskMedical device
Hill-Rom, Inc. recalls Centrella Smart+ Bed, Catalog Number P7900
Hill-Rom recalls Centrella Smart+ Bed (Catalog P7900) with serial codes from U290PF8145 to V015PF2473 and specific updated codes. The bed's exit system may fail to send remote alerts if previously canceled.
Hill-RomApr 30, 2020 - Use cautionMedical device
Medtronic Inc. recalls MiniMed 670G, insulin pump, Ref/Model # MMT-1760KPK, MMT-1762KCN, MMT-1762WWK - Product Usage: indicated for continuous
Medtronic recalls MiniMed 670G insulin pumps with serial numbers ending in H (e.g., NG2093124H) due to missing solder battery connection that could interrupt insulin delivery.
MedtronicApr 30, 2020 - Lower riskMedical device
Diasol, Inc recalls DIASOL 1000225-10-DEX100 LIQUID ACID CONCENTRATE FOR BICARBONATE DIALYSIS
Diasol recalls liquid acid concentrate for hemodialysis due to incorrect labeling of dialysate concentration. This could affect dialysis safety. Check your product's model number or UDI for details.
DiasolApr 30, 2020 - Use cautionMedical device
Siemens Medical Solutions USA, Inc recalls Multi Display Manager in the Artis Systems (Image-Intensified Fluoroscopic X-Ray System) as follows: Artis Q floor
Siemens recalls specific Artis Q floor and ceiling X-ray system Multi Display Managers due to potential electrical contact issues causing procedure interruptions. Affected models include Artis Q floor (10848280) and ceiling (10848281) units.
SiemensApr 30, 2020 - Lower riskMedical device
Cook Inc. recalls Pressure Monitoring Set, C-PMS, G02838
Cook recalls Pressure Monitoring Set C-PMS G02838 with lot numbers 8910219-10148417 due to potential excess coating on needles that could cause blockage during use.
CookApr 30, 2020 - Lower riskMedical device
Normand-Info S.A.S.U. recalls Remisol Advance running Software Version 1.12 The Normand Info Remisol Advance Data Manager collects and manages data
Normand Info recalls Remisol Advance software version 1.12 due to potential deletion of critical blood test results, affecting accurate WBC, UWBC, and PLT counts.
Normand InfoApr 30, 2020 - Lower riskMedical device
Elekta, Inc. recalls Elekta Unity, UDI 05060191071321, Image-guided radiation therapy system - Product Usage: is indicated for radiation
Elekta recalls Unity radiation therapy systems with serial numbers 600001-600043 due to potential Legionella in heat exchanger condensation tray. Affected units may need cleaning or inspection.
ElektaApr 30, 2020 - Use cautionMedical device
Covidien Llc recalls Dover 100% Silicone Silver-Hydrogel Coated Foley Catheter with Temperature Sensor 16FR 5CCCC2W, Product Code: 50516ICT
Covidien recalls 16FR silicone coated foley catheters with temperature sensors due to potential inaccurate temperature readings, which could lead to incorrect diagnoses and inadequate treatment. Affected units were sold with specific product codes and lot numbers.
CovidienApr 30, 2020 - Stop using nowConsumer product
Ximi Vogue Recalls Children's Neck Pillows Due to Violation of the Federal Lead Paint Ban; Risk of Poisoning
Ximi Vogue recalls four children's neck pillow models due to lead paint in zippers. Lead poisoning risk for young children. Consumers should stop using and get a refund.
Ximi VogueApr 30, 2020 - Stop using nowConsumer product
Modular Robotics Recalls Rechargeable Battery Packs Due to Burn Hazard
Modular Robotics recalls rechargeable battery packs that can overheat and cause burns. Consumers should stop using and return for free replacement.
Modular RoboticsApr 30, 2020 - Stop using nowConsumer product
Essential Trading Post Recalls Wintergreen and Birch Essential Oils Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
Essential Trading Post recalls Wintergreen and Birch essential oils due to non-child-resistant packaging. Risk of poisoning if swallowed by children. Full refund available.
Essential Trading PostApr 30, 2020 - Use cautionConsumer product
Bellman & Symfon Recalls Flash Receivers for Reduced Hearing Persons; Unit Can Fail to Alert in an Emergency
Bellman & Symfon Flash Receivers (BE1442 MHz) may fail to alert hearing-impaired users during emergencies due to battery charging problems. Affected units require free repair to prevent missed emergency alerts.
Bellman & SymfonApr 30, 2020 - Use cautionVehicle
MCI D4505 (2017) recall — Seat Belts
Motor Coach Industries is recalling 2017 D4505 buses with seat belts that may not extend from retracted position, increasing crash injury risk. Owners must contact MCI for free seat belt replacement.
MCIApr 29, 2020 - Use cautionVehicle
BMW 530I (2017) recall — Air Bags
BMW is recalling 2017 530i models due to potential head air bag deployment issues after crashes. Affected vehicles may need free air bag replacement to prevent injury risks.
BMWApr 29, 2020 - Use cautionVehicle
GILLIG LOW FLOOR (2019) recall — Fuel System, Other
Gillig recalls certain 2018-2020 CNG low floor transit buses due to fuel system rupture risk from heat exposure. Affected owners should contact customer service for free replacement.
GilligApr 29, 2020 - Use cautionVehicle
VOLVO VNR (2021) recall — Steering
Volvo is recalling certain 2020-2021 VNR trucks due to loose steering gear fasteners that may cause loss of vehicle control. Owners should contact customer service for free repairs.
Volvo TrucksApr 29, 2020 - Lower riskMedical device
Thermo Fisher Scientific (Monterrey) recalls Samco Bio-Tite Sterile Specimen Container, 120mL/53mm, Bio-Tite Blue Cap Catalog Number: 07 0006 The specimen
Thermo Fisher Scientific recalls Samco Bio-Tite Sterile Specimen Containers (120mL) that were not properly irradiated, making them non-sterile and potentially unsafe for lab use. Affected containers have specific catalog numbers and expiration dates.
Thermo Fisher ScientificApr 29, 2020 - Lower riskFood
Ricker Hill Farms, Inc. recalls RICKER HILL ORCHARDS APPLE CIDER McIntosh Blend, 1 GAL (128 FL OZ) and 1/2 GAL (64 FL OZ); UPC: 0 74613 80009 8; MADE
Ricker Hill Farms recalls apple cider with high patulin levels. Patulin is a mold toxin that can cause health issues. Consumers should check UPC 074613800098 for affected products.
Ricker HillApr 29, 2020 - Use cautionVehicle
TRIUMPH SPEED TRIPLE S (2019) recall — Service Brakes, Hydraulic
Triumph is recalling 2019 Speed Triple S motorcycles with front brake pads that may detach, increasing crash risk. Owners must have front brake pads replaced free by June 26, 2020.
TriumphApr 28, 2020 - Use cautionMedical device
GE Healthcare, LLC recalls Giraffe Incubator with installed Servo Oxygen module. Infant incubator.
GE Healthcare recalls infant incubators with Servo Oxygen modules that may display incorrect oxygen levels, risking infant health. Affected units have specific serial numbers and part kits.
GE HealthcareApr 28, 2020 - Lower riskFood
Glaxosmithkline Consumer Healthcare Holdings recalls Benefiber Healthy Shape Prebiotic Fiber Supplement, 500G UPC 886790018872
Glaxosmithkline recalls Benefiber Healthy Shape Prebiotic Fiber Supplement (500g, UPC 886790018872) due to potential contamination with small plastic pieces. Consumers should check their product and contact the company for details.
GlaxosmithklineApr 28, 2020 - Use cautionVehicle
BLUE BIRD VISION (2017) recall — Parking Brake
Blue Bird is recalling 2009-2019 Vision transit buses with a parking brake that may not hold the vehicle stationary on inclines when fully loaded, risking injury to bystanders. Owners must have the brake inspected by dealers by June 24, 2020.
Blue BirdApr 27, 2020 - Use cautionVehicle
BLUE BIRD VISION (2017) recall — Parking Brake
Blue Bird is recalling certain 2006-2021 Vision and 2007-2013 All American school buses due to a parking brake that may fail to hold the vehicle on inclines when fully loaded, risking crashes. Owners must have the brake inspected and corrected free by June 24, 2020.
Blue BirdApr 27, 2020 - UnratedMedical device
Philips North America, LLC recalls Philips HeartStart MRx Monitor/Defibrillators Model numbers M3535A, M3536A, and M3536M - Product Usage: is for use for
Philips recalls HeartStart MRx Defibrillators with model numbers M3535A, M3536A, and M3536M that may not have been included in prior field actions and received required corrections. Serial numbers listed.
PhilipsApr 27, 2020 - Use cautionMedical device
Defibtech, LLC recalls DDU-2450 Lifeline ECG Model Numbers DDU-A2450EN DDU-E2450DE DDU-E2450EN DDU-E2450FR DDU-E2450TH Cat. No. DCF-A2460EN
Defibtech recalls DDU-2450 Lifeline AEDs with specific model numbers and serials due to risk of failing to deliver shock during cardiac arrest emergencies.
DefibtechApr 27, 2020 - Use cautionFood
Condies Foods, Inc. recalls 43559 SNDW Chicken Sandwich on White Single, vacuumed pack bag, Clam shell. Label UPC: 50777444804, Condies Foods Inc.
Condies Foods recalls 43559 SNDW Chicken Sandwich due to undeclared soy allergen in the product. This could cause allergic reactions in people with soy allergies.
Condies FoodsApr 27, 2020 - Use cautionMedical device
Argon Medical Devices, Inc recalls Skater Introducer Set 6F x 18cm. REF/UDI: 651506300/(01)00886333005000; 655506300/(01)00886333005079 - Product Usage:
Argon Medical recalls Skater Introducer Set 6F x 18cm due to risk of tungsten coils detaching from guidewires during use in non-vascular procedures.
Argon MedicalApr 26, 2020 - Use cautionFood
Middle East Bakery, Inc. recalls Joseph's Gluten Free Original Wrap, 4 wraps, Net. Wt. 5.6 oz., UPC Code: 074117-003612
Middle East Bakery recalls gluten-free wraps due to gluten contamination. Consumers should check UPC 074117-003612 for affected products.
Joseph's Gluten FreeApr 25, 2020 - Use cautionVehicle
LINCOLN MKZ (2016) recall — Exterior Lighting
Ford is recalling 2016 Lincoln MKZ headlamps with improper beam patterns that could reduce driver visibility and increase crash risk. Owners must have headlamps inspected and replaced free of charge by dealers.
FordApr 24, 2020 - Lower riskMedical device
Abbott Gmbh & Co. KG recalls ARCHITECT iGentamicin Reagent Kit - Product Usage: The measurements obtained are used in the diagnosis and treatment of
Abbott recalls ARCHITECT iGentamicin Reagent Kit (model 1P31-25) due to possible inaccurate test results when used with certain troponin tests. Affected lots: 04281BE00 (until May 2020), 08510BE00 (until Aug 2020), 11221BE00 (until Nov 2020).
AbbottApr 24, 2020
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