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
35,025 found- Use cautionMedical device
Terumo Cardiovascular Systems Corporation recalls Terumo Advanced Perfusion System 1 Electronic Patient Gas System Catalog #: 801188
Terumo recalls its Advanced Perfusion System 1 Electronic Patient Gas System (Catalog #801: 801188) due to intermittent failure causing blender initialization faults during calibration. Affected units may have disabled control sliders.
TerumoJun 8, 2021 - Lower riskMedical device
RAYSEARCH LABORATORIES AB recalls RayStation (Radiation Treatment Planning System) : RayStation 9A, 9B, 9B SP1, 10A, 10A SP1, 10B and 11A, in combination
RaySearch Laboratories recalls RayStation versions 9A-11A with incorrect beam delivery positions. Affected software versions may cause treatment errors if used without correction.
RaySearch LaboratoriesJun 8, 2021 - Lower riskMedical device
Philips North America Llc recalls 728333 Spectral CT 7500 -Computed Tomography X-ray system
Philips recalls Spectral CT 7500 X-ray systems that may increase contrast volume when set to pounds, potentially affecting patient imaging safety. Affected units have specific serial numbers and software versions.
PhilipsJun 8, 2021 - UnratedDrug
Bausch Health Companies, Inc. recalls Mephyton (Phytonadione) 5 mg tablets, 100-count tablets, Rx Only, Manufactured for: Valeant Pharmaceuticals North
Baus: Health recalls Mephyton 5mg tablets (NDC 0187-1704-05) manufactured for Valeant. Failed impurities could cause harm. Check lot numbers 19D012P (exp 07/2021) or 20D096P (exp 10/2022).
Bausch HealthJun 8, 2021 - Lower riskDrug
Prisma Health Outsourcing Facility recalls Ketamine HCl Injection Solution, 10 mg / 2 mL (5 mg/mL), Rx Only, Compounded by Prisma Health Outsourcing Facility 1071
Prisma Health recalls ketamine injections with incorrect expiry dates. Products may expire before intended use, risking ineffective treatment or safety issues.
Prisma HealthJun 8, 2021 - Lower riskFood
Beechnut Nutrition recalls Beech-Nut brand Single Grain Rice Baby Cereal; NET WT. 8 OZ (227g); INGREDIENTS: Rice flour, sunflower lecithin;
Beechnut Nutrition recalls single-grain rice baby cereal due to potential elevated arsenic levels. Consumers should check product details and follow safety instructions.
BeechnutJun 8, 2021 - Lower riskFood
FO-ND, LLC. (dba Firebird Artisan Mills) recalls Firebird Artisan Mills Gluten Free Organic Brown Rice Flour, Net Wt: 50 lb / 22.7 kg. 500 North St W., Harvey, ND 58341
Firebird Artisan Mills recalls gluten-free organic brown rice flour due to potential Salmonella contamination. Consumers should check lot numbers and contact the company for details.
Firebird Artisan MillsJun 8, 2021 - Use cautionVehicle
NORTHWOOD ARCTIC FOX (2019) recall — Equipment
Northwood is recalling 2019 Arctic Fox campers with Dometic stoves due to potential gas leaks causing fire risk. Owners must contact service for free repairs.
NorthwoodJun 7, 2021 - Lower riskMedical device
BioFire Diagnostics, LLC recalls FilmArray Pneumonia Panel (Pneumo) Part Numbers: Part No: RFIT-ASY-0144 / UDI: 00815381020178 (30 test kit) Part No:
BioFire Diagnostics recalls pneumonia test kits that may give false negative results after 6 months of use. Affected kits have specific part numbers and serial codes. Stop using if expired.
BioFire DiagnosticsJun 7, 2021 - Use cautionMedical device
Medtronic Vascular, Inc. recalls Endurant II/Endurant IIs Stent Graft System: Medtronic Endurant II Stent Graft System REF ETUF3214C102EE,
Medtronic recalls Endurant II stent graft systems with specific model numbers due to risk of radiopaque marker detaching during deployment, potentially causing complications.
MedtronicJun 7, 2021 - Lower riskMedical device
Pear Therapeutics, Inc. recalls reSET-O Mobile App, iOS and Android, provides cognitive behavioral therapy, as part of substance abuse treatment.
Pear Therapeutics recalls reSET-O Mobile App for substance abuse treatment. The app may show reward wheel spins for users with positive urine drug screens, which should not happen. Users should contact the company for details.
Pear TherapeuticsJun 7, 2021 - Use cautionVehicle
MERCEDES-BENZ SPRINTER 4500 (2020) recall — Steering
Mercedes-Benz is recalling 2020 Sprinter 4500 vehicles due to potential power steering fluid leaks causing sudden loss of steering assist. Owners must contact DVUSA for free clamp installation.
Mercedes-BenzJun 4, 2021 - Use cautionVehicle
ARCIMOTO FUV (2020) recall — Electrical System
Arcimoto is recalling 2019-2021 FUV and related electric motorcycles due to potential battery shutdown without warning, which could increase crash risk. Owners will receive free firmware updates.
ArcimotoJun 4, 2021 - Lower riskMedical device
Eight Medical International BV recalls Recirculator 8.0s Disposable Lavage Kit (product code number 8100) , GTIN: 08719992086016. Hyperthermic Perfusion
Eight Medical recalls Recirculator 8.0s Disposable Lavage Kits (product code 8100) due to potential aluminum ion release during warming therapy. Affected units include specific lot numbers from 19854184 to 20202106.
Eight MedicalJun 4, 2021 - Lower riskMedical device
Baxter Healthcare Corporation recalls Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009. for the controlled administration of
Baxter recalls Spectrum IQ Infusion System with Dose IQ Safety Software (Product Code 3570009) due to network configuration errors causing pump connectivity issues. Affected units may experience infusion errors.
Baxter HealthcareJun 4, 2021 - Lower riskMedical device
GE Healthcare, LLC recalls SIGNA Premier - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high
GE Healthcare recalls SIGNA Premier MRI scanners where accidentally selecting patient orientation may cause flipped images. Affected units require correction to prevent misdiagnosis.
GE HealthcareJun 4, 2021 - Lower riskMedical device
Simpleware Product Group, SYNOPSYS NORTHERN EUROPE recalls Simpleware ScanIP software. For transfer of imaging information from a medical scanner to an output file, and for
Simpleware recalls ScanIP software versions 7.0, 2016.09, M-2017.06, and N-2018.03 due to potential incorrect anatomical labels causing medical imaging errors. Affected users should contact Simpleware for updates.
SimplewareJun 4, 2021 - UnratedDrug
Dr. Reddy's Laboratories, Inc. recalls Atorvastatin Calcium Tablets, USP 10 mg, 500-count bottles, Rx Only, Dr. Reddy's Mfd. By: Dr. Reddy's Laboratories
Dr. Reddy's recalls 10mg Atorvastatin tablets due to impurities that could affect safety. Affected lots from 2021 with specific NDC numbers. Consumers should contact the manufacturer for details.
Dr. Reddy'sJun 4, 2021 - Lower riskFood
Olde Thompson, LLC recalls Olde Thompson Organic Ground Coriander 1.5oz. in glass jar with flip-top lid. Sun Harvest Organic Coriander 1.5oz in
Olde Thompson recalls organic ground coriander jars with potential Salmonella contamination. Affected items have specific UPC codes and lot numbers. Consumers should check labels and contact the company for details.
Olde ThompsonJun 4, 2021 - Lower riskFood
Tulkoff Food Products, Inc. recalls Tulkoff Spicy Kimchi Aioli, 18 fl oz Clear Plastic Squeeze bottle, item number 098001, lot number 09.18.2021M, 8
Tulkoff Food Products recalls 18 fl oz Spicy Kimchi Aioli bottles due to undeclared soy and wheat allergens. Consumers should check product labels for item number 098001 and lot number 09.18.2021M.
TulkoffJun 4, 2021 - Stop using nowFood
Lakeview Farms LLC recalls Smilin' Bob's All Natural Smoked Fish Dip 8 oz plastic container 12 per case
Lakeview Farms recalls Smilin' Bob's All Natural Smoked Fish Dip due to potential Listeria monocytogenes contamination. Consumers should check lot codes and discard affected products.
Lakeview FarmsJun 4, 2021 - Stop using nowFood
Bomunity Ltd Co recalls Paximune Dietary Supplement Contains Bovine Proteins that help Promote Health and help Modulate Immunity 2 Fl. Oz.
Bomunity Ltd Co recalls Paximune Dietary Supplement due to potential bacterial contamination. Check lot 210402 and UPC 64395 00001.
BomunityJun 4, 2021 - Lower riskMedical device
Ethicon Endo-Surgery Inc recalls ECHELON FLEX Powered Plus Stapler-intended for transection, resection, and/or creation of anastomoses. The instruments
Ethicon recalls ECHELON FLEX Powered Plus Stapler devices labeled as 60mm but containing 45mm devices. This mislabeling may cause surgical errors. Affected units have specific product codes and expiration dates.
EthiconJun 3, 2021 - Use cautionMedical device
Boston Scientific Corporation recalls INLIVEN CRT-P, Model Numbers: a) V284 b) V285 c) W274 d) W275 (added 7/15/2021)
Boston Scientific recalls specific INLIVEN CRT-P pacemakers (models V284, V285, W274, W275) with Extended Life batteries that may initiate Safety Mode, causing temporary system resets. Replacement is required.
Boston ScientificJun 3, 2021 - UnratedMedical device
Axonics Modulation Technologies, Inc. recalls BULKAMID, URETHRAL BULKING SYSTEM model # 50050 containing the component: Bulkamid Needle, REF 230651221C, 2 G x 12 am,
Axonics recalls BULKAMID urethral bulking system model 50050 with potential sterility issues in needle components. Affected units may not have been properly sterilized, risking infection during medical procedures.
AxonicsJun 3, 2021 - Use cautionMedical device
Heartware, Inc. recalls HeartWare HVAD Pump Implant Kit, REF 1125
Heartware recalls HVAD Pump Implant Kit REF 1125 due to higher neurological adverse events and mortality risks compared to other LVADs, with internal pump failure concerns.
HeartwareJun 3, 2021 - Lower riskMedical device
Boston Scientific Corporation recalls Accolade pacemaker, Models: a) L300 b) L301 c) L310 d) L311 e) L321 f) L331
Boston Scientific is a global leader in medical devices, surgical tools, and implants. We provide innovative solutions for cardiovascular, neurovascular, and other medical procedures.
Boston ScientificJun 3, 2021 - Stop using nowConsumer product
Kalorik Recalls Electric Steakhouse Grills Due to Shock Hazard (Recall Alert)
Kalorik recalls Pro 1500F Electric Steakhouse Grills with incorrectly electroplated knobs that can cause electric shock after full preheating. Consumers must stop using and contact Kalorik for free repair kits.
KalorikJun 3, 2021 - Stop using nowConsumer product
Fisher-Price Recalls 4-in-1 Rock 'n Glide Soothers After Four Infant Deaths; 2-in-1 Soothe 'n Play Gliders Also Recalled
Fisher-Price recalls 4-in-1 Rock 'n Glide Soothers and 2-in-1 Soothe 'n Play Gliders after infants placed unrestrained on stomach face suffocation risk. Consumers must stop using and get refunds.
Fisher-PriceJun 3, 2021 - Use cautionMeat & poultry
FSIS Issues Public Health Alert for Frozen Raw Breaded Stuffed Chicken Products Due to Possible Salmonella Contamination
FSIS warns of possible Salmonella Enteritidis in frozen raw breaded stuffed chicken. Learn symptoms, cooking safety tips, and who is at risk.
FSISJun 2, 2021
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