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 riskFood
Kindroot LLC recalls kindroot adaptogems; Peach Blossom Plant lozenges for lit looks. 20 lozenges net wt. 2.6 oz. 74 g - Dietary Supplement
Kindroot recalls Peach Blossom Plant lozenges for dietary supplements due to missing fish as collagen source. Label error may mislead consumers about collagen content.
KindrootJan 15, 2020 - Lower riskFood
The Honest Stand recalls Hungry Root Dairy free Garlic Parm sauce, Packaged in 9 oz. polypropylene dip containers with lidding film and lid,
The Honest Stand recalls Garlic Parm sauce due to undeclared cashews and almonds in the product. Both allergens were labeled electronically but not on physical packaging.
The Honest StandJan 15, 2020 - Lower riskMedical device
Medtronic CoreValve LLC recalls Medtronic Simulus 850 Semi Rigid Ring/Band Accessory Kit Used to size a patient's mitral or tricuspid valve in cardiac
Medtronic recalls Simulus 850 Semi-Rigid Ring/Band Accessory Kits due to potential porcine tissue contamination in demonstration kits. This affects cardiac procedure kits used for valve sizing.
MedtronicJan 14, 2020 - Use cautionMedical device
Philips North America, LLC recalls Ambulance Parameter Extension (APE) kit M4758A, an accessory to the Philips HeartStart MRx Monitor/Defibrillator -
Philips recalls ambulance parameter extension kit M475: May cause ECG leads to go off in hot, humid environments. Affected units were sold to EMS providers. No remedy specified.
PhilipsJan 14, 2020 - Lower riskMedical device
Abbott Point Of Care Inc. recalls i-STAT G3+ cartridge (blue), List No. 03P78-50, UDI (01) 00054749002283 - Product Usage: The i-STAT G3+ cartridge may
Abbott recalls blue i-STAT G3+ cartridges due to insufficient clinical evidence for safety and performance. All units are affected; stop using immediately to avoid potential risks.
AbbottJan 14, 2020 - Use cautionMedical device
CME America, LLC recalls BodyGuard Microset For Use with the BodyGuard Infusion Pump *** Tubing: 110 in. (280 cm) - Blue Stripe - Product Usage:
CME America recalls BodyGuard Microset tubing with potential incorrect filter pore size that could affect medication delivery safety.
CME AmericaJan 14, 2020 - Lower riskMedical device
Ormco/Sybronendo recalls Ormco Damon Q2 Orthodontic Metal Bracket, Part No. 491-9834, L3R Hi Tq Hook, Tq +13 degrees, Rx. Manufactured by Ormco
Ormco recalls Damon Q2 orthodontic brackets with mislabeled torque specifications. Affected units may have incorrect torque settings that could impact treatment safety.
OrmcoJan 14, 2020 - UnratedDrug
Spectrum Laboratory Products recalls Ranitidine Hydrochloride (powder), USP, Rx only, Spectrum Chemical Mfg Corp., a) 1 gram, b) 5 grams, c) 25 grams, d)100
Spectrum recalls ranitidine hydrochloride powder (1g-1kg) due to NDMA impurity detected. This chemical may pose health risks. Affected lots expire October 2023.
Spectrum Laboratory ProductsJan 14, 2020 - Use cautionDrug
Hikma Pharmaceuticals USA Inc. recalls methylPREDNISolone Sodium Succinate For Injection, USP, 500 mg*/vial, Rx Only, Mfd by: HIKMA FARMACEUTICA (PORTUGAL),
Hikma Pharmaceuticals recalls 4840 vials of methylPREDNISolone Sodium Succinate due to incorrect reconstitution instructions on the label.
Hikma PharmaceuticalsJan 14, 2020 - Lower riskDrug
Sun Pharmaceutical Industries, Inc. recalls Testosterone Cypionate for Injection, USP, 1,000 mg/10 mL (100 mg/mL), 10 mL Multiple Dose Vial (NDC 62756-017-40), Rx
Sun Pharmaceutical recalls specific testosterone injection vials due to manufacturing quality deviations. Affected lots were produced under similar conditions to a previously rejected batch. Consumers should contact the manufacturer for details.
Sun PharmaceuticalJan 14, 2020 - Lower riskDrug
Pharmaceutical Associates Inc recalls Nystatin Oral Suspension, USP 100,000 units per mL Cherry/Peppermint Flavor, 16 fl oz (473 mL) Rx Only, pai,
Pharmaceutical Associates recalls Nystatin Oral Suspension (16 fl oz) due to subpotent levels. This may not contain enough active ingredient for effective treatment. Consumers should contact the manufacturer for details.
Pharmaceutical AssociatesJan 14, 2020 - Stop using nowConsumer product
The Thompson's Company Recalls Aerosol Waterproofing Wood and Masonry Protectors Due to Fire Hazard
Thompson's WaterSeal waterproofing wood and masonry protectors in aerosol cans are recalled due to leaking propellant that can cause fires. Consumers should stop using and discard these products immediately for a full refund.
Thompson'sJan 14, 2020 - Use cautionVehicle
LEXUS RC 350 (2019) recall — Fuel System, Gasoline
Toyota Lexus recalls 2019 RC 350 vehicles with faulty fuel pump that may cause engine stalling while driving, increasing crash risk. Owners must contact Toyota or Lexus for free fuel pump replacement.
LexusJan 13, 2020 - Lower riskMedical device
Mindray DS USA, Inc. dba Mindray North America recalls DP-30 Digital Ultrasonic Diagnostic Imaging System, Part No. 1155E-PA00004 - Product Usage: The Digital Ultrasonic
Mindray recalls DP-30 ultrasound systems with 65EC10EA transducers that may display incorrect needle-guide brackets. This could affect imaging accuracy during medical exams.
MindrayJan 13, 2020 - Use cautionMedical device
Stryker Instruments Div. of Stryker Corporation recalls SafeAir Telescopic Smoke Evacuation Pencil, Product No. 0703 046 004. The product is a Bovie pencil that is 75 inches
Stryker recalls a 75-inch telescopic smoke evacuation pencil due to potential hairline fractures causing electrical arcing and burns to users or patients. Affected units have specific product numbers.
StrykerJan 13, 2020 - Lower riskMedical device
C.R. Bard Inc recalls The Bard Intra-abdominal Pressure Monitoring Device is composed of a tubing set used for infusing fluid into the
C.R. Bard recalls intra-abdominal pressure monitoring devices with potential for inaccurate readings due to leaks or disconnects near the sampling port. Users should confirm measurements with alternative methods.
C.R. BardJan 13, 2020 - Stop using nowMedical device
TELEFLEX MEDICAL INC recalls Pilling Aortic Punch, 4.0 mm Standard Tip, REF 353440
Teleflex Medical recalls Pilling Aortic Punch 4.0mm Standard Tip (REF 353440) due to potential packaging compromise affecting sterility. Affected units sold with lot number 74B1500674.
Teleflex MedicalJan 13, 2020 - Lower riskMedical device
Philips North America, LLC recalls Philips DigiTrak XT Holter Recorder Software version number B.1 and C.2. The DigiTrak XT Recorder is available in four
Philips recalls DigiTrak XT Holter Recorder software versions B.1 and C.2 (made before Dec 2019) that may display error 602 if AAA batteries are used or docked, causing failure during patient studies.
PhilipsJan 13, 2020 - Use cautionMedical device
CooperVision Inc. recalls Coopervision Vertex Toric /2 Clear Toric- Power -2.50 -0.75 /90 Soft (hydrophilic) Contact Lens (extended wear)
CooperVision is recalling specific lots of Vertex Toric contact lenses because the power may be incorrect. Check your lot numbers immediately.
CooperVisionJan 13, 2020 - Use cautionVehicle
HYUNDAI VELOSTER (2016) recall — Engine
Hyundai recalls 2016 Velosters with engine bearing damage that could cause fire or crash. Free repairs include engine replacement and software update. Contact 1-855-371-9460.
HyundaiJan 12, 2020 - Use cautionVehicle
HYUNDAI NEXO (2020) recall — Service Brakes, Hydraulic
Hyundai is recalling certain 2020 Nexo vehicles due to potential reduced braking power, which could increase crash risk. Owners must contact customer service for free software update.
HyundaiJan 12, 2020 - Use cautionVehicle
HORTON TYPE I (2020) recall — Electrical System
Halcore is recalling 2020 Horton Type I emergency vehicles with i4G Vivtech displays due to potential control panel failure causing emergency service delays. Affected vehicles may need repair to prevent injury risks.
HalcoreJan 12, 2020 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Reaction Ring Segment, SMN 11099326, UDI 00630414596143
Siemens Healthcare recalls Atellica CH Reaction Ring Segments with specific lot numbers due to potential water contamination that may cause inaccurate lab test results.
Siemens HealthcareJan 12, 2020 - Use cautionFood
Sugar Foods Corporation recalls Granulate Pure Cane Sugar sold under the brand names of: Ahold 16 oz canister, DISTRIBUTED BY FOODHOLD USA, LLC,
Sugar Foods Corporation recalls specific lots of Ahold, N'Joy, and Speedway granulated cane sugar due to potential foreign material contamination.
Sugar FoodsJan 12, 2020 - Lower riskFood
Cargill, Inc Corporate Headquarters recalls Marigold, INC. Granulated Cane Sugar Net Weight: 2000#
Marigold Inc. recalls 2000lb granulated cane sugar with foreign material. Consumers should check product labels for batch codes AB19L263B, AB19L273B, or AB19L271B.
MarigoldJan 12, 2020 - UnratedMedical device
Cardinal Health recalls AAMI 3 NONREIN SCRBNURGOWN BNS L, Item Code 90270NB
Cardinal Health recalls AAMI 3 non-reinforced surgical gowns with unknown bioburden and microbiological contamination. Affected gowns have specific lot numbers from 2018-2019 production. Consumers should contact manufacturer for details.
Cardinal HealthJan 11, 2020 - Use cautionMeat & poultry
Culinary International, LLC Recalls Chicken Burrito Products Due to Misbranding and Undeclared Allergens
USDA recalls 626 pounds of egg burritos labeled as chicken burritos due to undeclared eggs, a known allergen. Consumers urged to throw away or return products.
Culinary InternationalJan 10, 2020 - Use cautionVehicle
CADILLAC ESCALADE (2018) recall — Service Brakes, Hydraulic
GM recalls 2018 Cadillac Escalades with brake assist issues that may increase stopping distance. Owners must reprogram the brake control module for free by November 11, 2020.
CadillacJan 10, 2020 - Lower riskMedical device
BIOMERIEUX - Grenoble recalls NUCLISENS¿ Lysis Buffer, IVD, REF 200292, 48X2 ML LYS Manufacturer bioMerieux SA 376, Chemin de l'Orme 69280
bioMerieux recalls NUCLISENS Lysis Buffer (ref 200292) due to pH electrode drift causing invalid test results. Affected units have lot number 19040201.
bioMerieuxJan 10, 2020 - Use cautionMedical device
Terumo Cardiovascular Systems Corporation recalls Terumo Advanced Perfusion Assembly Pump Guts, 4 Inch, Catalog Number 801805 - Product Usage: is indicated for use for
Terumo recalls specific roller pumps that may fail due to noise, risking pump stoppage during blood circulation procedures. Affected units have serial numbers starting with 880559-882813 and 885541-885543.
TerumoJan 10, 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.