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 cautionConsumer product
B&B Acquisition Recalls Wintergreen Essential Oils Due to Failure to Meet Child Resistant Packaging Requirements; Risk of Poisoning
B&B Acquisition recalls wintergreen essential oils without child-resistant caps due to poisoning risk for young children. Consumers should store out of reach and get free replacements.
B&B AcquisitionNov 20, 2019 - Lower riskMeat & poultry
BrucePac Recalls Ready-to-Eat Chicken Sausage Products Due to Misbranding
BrucePac recalls 55,550 pounds of ready-to-eat chicken sausage products with pork casing not declared on labels. Products should be thrown away or returned to purchase location.
BrucePacNov 19, 2019 - Use cautionVehicle
THOMAS BUILT BUSES SAF-T-LINER HDX (2019) recall — Power Train
Daimler Trucks North America recalls 2018-2020 Thomas Built Saf-T-Liner HDX school buses with loose bolts that could disable the bus during traffic, requiring evacuation. Owners must contact DTNA for free inspection.
Thomas BuiltNov 19, 2019 - Use cautionVehicle
SPARTAN GLADIATOR (2020) recall — Service Brakes, Air
Spartan recalls 2020 Gladiator vehicles with unsecured brake air lines that could cause sudden brake application and crashes if lines are severed.
SpartanNov 19, 2019 - Use cautionVehicle
FOREST RIVER FLAGSTAFF (2020) recall — Tires
Forest River recalls 2020 Flagstaff trailers with improper tire clearance that may cause tire failure and loss of vehicle control. Owners must have a new outrigger installed or damaged tires replaced.
Forest RiverNov 19, 2019 - Use cautionMedical device
Dexcom Inc recalls Brand Name: Dexcom G6 CGM App for iOS Software Number: SW11677 Software Version: Version 1.4.0 up to corrected Version
Dexcom recalls iOS software version 1.4.0 of its G6 CGM app up to 1.4.4 due to low alarm feature not alerting users after 30 days of app installation. This could lead to undetected high blood sugar levels.
DexcomNov 19, 2019 - Lower riskMedical device
Cardiac Assist, Inc recalls TandemLife ECLS Procedure Kit - V24/A17, Catalog Number 5740-2417 - Product Usage: The function of the 24Fr ProtekSolo
Cardiac Assist recalls TandemLife ECLS Procedure Kit V24/A17 (Catalog 5740-2417) due to incorrect cannula size. This kit contains a 29Fr ProtekDuo instead of the required 24Fr ProtekSolo, which could lead to improper blood flow during cardiac support procedures.
Cardiac AssistNov 19, 2019 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls ADVIA Chemistry CardioPhase High Sensitivity C-Reactive Protein (hsCRP) Calibrator - product Usage: For in vitro
Siemens Healthcare recalls ADVIA hsCR:RP calibrators due to accuracy drift causing high bias in patient samples. Affected units may need recalibration or replacement.
Siemens HealthcareNov 19, 2019 - Lower riskMedical device
Angiodynamics, Inc. recalls OARTRAC PROSTATE IMMOBILIZATION ENDORECTAL BALLOON DEVICE KIT, Catalog Number: ORB-60F - Product Usage: pre-calibrated
Angiodynamics recalls prostate immobilization balloon kits with catalog number ORB-60F due to potential inaccurate radiation therapy readings. Affected units were sold with specific lot numbers and UDI codes.
AngiodynamicsNov 19, 2019 - Use cautionMedical device
Philips Respironics, Inc. recalls Trilogy EVO Ventilator, Nordics - Model Number: ND2110X15B Trilogy Evo is intended for pediatric through adult patients
Philips Respironics recalls Trilogy EVO Ventilators with specific software versions due to power alarm failure risk. Affected models include ND2110X15B with serial numbers listed. This defect may cause loss of critical safety alerts.
Philips RespironicsNov 19, 2019 - Lower riskDrug
AuroMedics Pharma LLC recalls Gabapentin Capsules, USP 100 mg, Rx Only, Distributed by: Aurobindo Pharma USA, Inc. Dayton, NJ 08810, NDC 65682-198-99
AuroMedics Pharma LLC recalls Gabapentin 100mg capsules (NDC 65682-198-99) due to foreign Losartan/HCTZ tablets found in some bottles. This may cause confusion with other medications.
AuroMedicsNov 19, 2019 - Stop using nowDrug
Baxter Healthcare Corporation recalls 0.9% Sodium Chloride Irrigation USP 5000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL 60015, NDC
Baxter Healthcare recalls 5000mL IV bags with potential leaks. Stop using if you have these bags. No remedy provided in official notice.
Baxter HealthcareNov 19, 2019 - Lower riskFood
GH IMPORTS, INC recalls Onion Minced: 16-40 Mesh, Net Weight: 24/kg/52.91lbs, Manufacturing Date: May, 2019, Country of Origin: China,
GH Imports recalls onion minced product (24kg/52.91lbs) from May 2019 with metal filament found in packages. Consumers should check for metal fragments before use.
GH ImportsNov 19, 2019 - Stop using nowConsumer product
United National Closeout Stores Recalls Isometric Exercise Devices Due to Projectile Hazard; Devices Sold at Burlington Stores After 2014 Recall
UNCS recalls ISO7X isometric exercise devices with black handle grips due to risk of parts ejecting during use. Consumers must stop using and get a refund.
UNCSNov 19, 2019 - Stop using nowConsumer product
Flying Tiger Copenhagen Recalls Crocodile Candleholders Due to Fire Hazard
Flying Tiger Copenhagen recalls gold crocodile candleholders that can catch fire when burning. Stop using immediately and get a full refund.
Flying Tiger CopenhagenNov 19, 2019 - Use cautionVehicle
DUCATI MULTISTRADA 1260 (2018) recall — Structure
Ducati is recalling 2018 Multistrada 1260 motorcycles due to potential side stand weld issues that could cause the bike to fall over, increasing injury risk. Owners must have the side stand replaced free by January 2, 2020.
DucatiNov 18, 2019 - Use cautionVehicle
BMW X6 (2019) recall — Child Seat
BMW recalls 2015-2019 X6 models with rear seat lower anchor bars that may damage child seats during crashes. Owners must contact BMW for free repairs to prevent injury risks.
BMWNov 18, 2019 - Lower riskMedical device
Southwest Technologies Inc recalls Elasto-Gel Absorbent Wound Dressing, Item DR8000. 5 Dressings 4" x 4". Sterile. UPC 45713-58000 Bacteriostatic
Southwest Technologies recalls 5 sterile Elasto-Gel wound dressings (4" x 4") with UPC 45713-58000 that may be contaminated with mold. Consumers should check lot numbers and contact the company for details.
Southwest TechnologiesNov 18, 2019 - Lower riskMedical device
W. L. Gore & Associates Inc. recalls Gore DrySeal Flex Introducer Sheath, Catalog #DSF1433, 33cm 14FR, Sterile. The responsible firm on the label is W. L.
W. L. Gore recalls sterile 14Fr DrySeal Flex Introducer Sheaths mislabeled as 14Fr when they are 16Fr. Check serial numbers for affected units.
W. L. GoreNov 18, 2019 - Lower riskMedical device
Paltop Advanced Dental Solutions Ltd recalls Paltop Dynamic Dental Implant Dia 3.25mm L 13.0 mm, Catalog Number 21-70020
Paltop recalls specific dental implants due to incorrect screw packaging. The Standard Platform Cover Screw won't fit the Narrow Platform implant, causing potential misfit issues.
PaltopNov 18, 2019 - Use cautionMedical device
Nucletron BV recalls There is a complaint regarding internal check cable guide mechanism failure for the Nucletron Flexitron brachytherapy
Nucletron recalls Flexitron brach: Internal cable guide mechanism failure may cause treatment interruptions or incorrect radiation positioning. Affected units have specific UDI codes.
NucletronNov 18, 2019 - Lower riskMedical device
Diagnostica Stago, Inc. recalls STA SYSTEM CONROL N + P (ref. 00678)
Diagnostica Stago recalls STA System Control N+P (ref. 00678) due to positive bias in factor VIII/IX testing compared to international standards. Affected lots may cause inaccurate blood test results.
Diagnostica StagoNov 18, 2019 - Use cautionMedical device
Boston Scientific Corporation recalls Habib EUS RFA, 10mm electrode active tip, Material Number/UPN: 6500 - Product Usage: The Habib EUS RFA is indicated for
Boston Scientific recalls Habib EUS RFA 10mm electrode active tips (Material Number 6500) due to risk of thermal injury from capacitive coupling with un-insulated needles. Affected units include specific batches with expiration dates.
Boston ScientificNov 18, 2019 - Lower riskMedical device
LivaNova USA Inc. recalls LivaNova USA Sterile Disposable Connector,1/2x1/2, 20 units per case
LivaNova recalls sterile disposable connectors with a 3/8x1/4 reducer instead of 1/2x1/2. No health risk expected as the mismatched size prevents use.
LivaNovaNov 18, 2019 - Use cautionMedical device
RAYSEARCH LABORATORIES AB recalls RayStation stand-alone software treatment planning system, Model Numbers 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3,
RaySearch recalls specific versions of RayStation treatment planning software due to a bug that may set beam dose to default values, requiring recalibration before treatment approval.
RaySearchNov 18, 2019 - Lower riskMedical device
Leica Microsystems, Inc. recalls BOND Polymer Refine Detection Kit, Catalog No. DS9800. This detection system is for in vitro diagnostic use. Bond
Leica recalls BOND Polymer Refine Detection Kit (DS9800) due to potential suboptimal staining from prolonged refrigeration. Affected kits may not stain tissue properly in lab use.
LeicaNov 18, 2019 - Use cautionMedical device
Viewray, Inc. recalls ViewRay System: Model No. 10000 and 20000 for radiation treatment. PN11440 MRIdian System Treatment Planning and
ViewRay System models 10000 and 20000 for radiation treatment may have misalignment in dose registration causing incorrect radiation doses. Affected units include specific serial numbers listed in the recall notice.
ViewRayNov 18, 2019 - Stop using nowFood
Honey Heaven Wholesale Inc recalls Hummingbird Wholesale Organic Chia Seeds, SD120-5#, packaged in a clear plastic bag with a while label, net wt. 5 lbs.
Hummingbird Wholesale recalls Organic Chia Seeds due to a metal bar hazard. Check your lot number and packaging details immediately.
Hummingbird WholesaleNov 18, 2019 - Stop using nowFood
Stern Produce Company Inc. recalls Queen Victoria Sweet Baby Broccoli from Ippolito International, packed in ice in half bushel boxes, 18 count
Stern Produce recalls Queen Victoria Sweet Baby Broccoli due to potential bacterial contamination from dripping ice water. Check your lot codes.
Queen VictoriaNov 18, 2019 - Lower riskFood
Nectar Foods Inc. recalls Honey Mama s Truffle Bar (Trader Joe's) is a honey cocoa bar, refrigerated, one bar is packaged in flexible film, flow
Nectar Foods recalls Honey Mama Truffle Bars (Trader Joe's) due to unintentional milk presence not listed on labels. Consumers should check for lot code 042620 and contact Nectar Foods for details.
Nectar FoodsNov 18, 2019
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