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
34,894 found- Use cautionMedical device
Stryker Communications recalls Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel, a component of Berchtold Chromophare Ceiling Mounted
Stryker recalls Berchtold Chromophare Dual Monitor Carrier Arms with possible insufficient welds. Affected units have specific serial numbers in the US and Canada. Stop using immediately to prevent potential failure.
StrykerJan 26, 2018 - Use cautionMedical device
RAYSEARCH LABORATORIES AB recalls Ray Station 4.9 Ray Station 5, Ray Station 6 and Ray Station 7 Software build numbers: 4.9.0.42, 5.0.0.37, 5.0.1.11,
RaySearch Laboratories recalls RayStation 4.9-7 software versions with incorrect treatment volume delivery risk. Affected units may require software update to prevent patient safety issues.
RaySearch LaboratoriesJan 26, 2018 - Lower riskMedical device
Siemens Medical Solutions USA, Inc. recalls Biograph Horizon - PET/CT, PETsyngo VJ20A Software Nuclear medicine/ xray diagnostic scanner.
Siemens recalls Biograph Horizon PET/CT scanners with VJ20A software due to potential image distortion from improper PET QC phantom positioning. Affected units may require software updates or corrections to ensure accurate imaging.
SiemensJan 26, 2018 - Lower riskMedical device
bioMerieux, Inc. recalls bioMerieux VITEK 2 Gram Positive Cefoxitin Screen, VITEK 2 Gram Positive AST for Oxacillin, VITEK SYSTEMS General
bioMerieux recalls VITEK 2 Gram Positive Cefoxitin and Oxacillin test kits due to increased non-detected MRSA cases. Affected kits have specific UDI numbers and are used in lab testing.
bioMerieuxJan 26, 2018 - Use cautionMedical device
Ion Beam Applications S.A. recalls Proteus 235, ProteusPLUS or Proteus ONE produces and delivers a proton beam for the treatment of patients with
Ion Beam Applications recalls Proteus 235, ProteusPLUS, and Proteus ONE proton therapy devices with PTS-7.X.X or PTS-8.X.X software versions. Switching treatment modes may cause under-irradiation or delayed patient treatment with extra X-ray exposure.
Ion Beam ApplicationsJan 26, 2018 - UnratedDrug
Primus Pharmaceuticals, Inc. recalls Limbrel (flavocoxid 500 mg) capsules, 60-count bottle, Rx only, Manufactured for: Primus Pharmaceuticals, Inc.,
Primus Pharmaceuticals recalls unapproved Limbrel capsules (flavocoxid 500mg) due to lack of FDA approval. These products have not been proven safe or effective and may pose health risks.
Primus PharmaceuticalsJan 26, 2018 - Stop using nowFood
Hanover Foods Corporation recalls Frozen Sliced (blanched) Squash packed in 1400 lb. plastic totes.
Hanover Foods recalls frozen sliced squash from specific lots due to Listeria monocytogenes contamination. Consumers should check lot numbers and contact Hanover for details.
Hanover FoodsJan 26, 2018 - Lower riskFood
Elwood International, Inc. recalls ELWOOD FAT-FREE LOW SODIUM RANCH DRESSING ARTIFICIAL FLAVOR. Single serve.
Elwood International recalls single-serve fat-free low sodium ranch dressing due to a missing scheduled process file. Check your fridge.
ElwoodJan 26, 2018 - Use cautionVehicle
HONDA CLARITY FUEL CELL (2017) recall — Electrical System
Honda recalls 2017 Clarity Fuel Cell vehicles with potential power loss causing crash risk. Free software update to fix electrical system issue.
HondaJan 25, 2018 - Use cautionVehicle
PALOMINO PALOMINI (2018) recall — Equipment
Forest River recalls 2018 Palomino Palomini trailers with potentially detachable LP propane bottles that could cause injury or crash. Owners must contact customer service for free ring replacement.
Forest RiverJan 25, 2018 - Lower riskMedical device
Medtronic Navigation, Inc.-Littleton recalls O-arm 1000 mobile image-intensified fluoroscopic x-ray system; (1) Model: BASE OARM Bl70000028100 SYS 100V, Product
Medtronic recalls O-arm 1000 mobile x-ray systems with specific model numbers for software update to fix power shutdown and image reconstruction problems.
MedtronicJan 25, 2018 - Lower riskMedical device
Stryker Corporation recalls CMI (Collagen Meniscus Implant) device, Ivy Sports Medicine s collagen-based meniscus implant Product Usage: The CMI
Stryker recalls collagen-based meniscus implants that may have been exposed to high temperatures during shipping, potentially affecting safety. Learn which models are affected and what to do.
StrykerJan 25, 2018 - Lower riskMedical device
GE Healthcare recalls Centricity PACS-IW with Universal Viewer Product Usage: Usage: Centricity PACS-IW with Universal Viewer is a device
GE Healthcare recalls Centricity PACS-IW with Universal Viewer devices that may show missing medical images without warning, risking incorrect diagnoses. Affected units include specific model numbers listed in the recall notice.
GE HealthcareJan 25, 2018 - UnratedDrug
PD-Rx Pharmaceuticals, Inc. recalls PD-Rx Pharmaceuticals Incorporated Ibuprofen 200 mg tablets a) 24 tablets NDC 55289-673-24; b) 30 tablets NDC
PD-Rx Pharmaceuticals recalls 200mg ibuprofen tablets with NDC codes 55289-673-24, 55289-673-30, 55289-673-50, and 55289-673-60 due to CGMP deviations. Consumers should check their product labels.
PD-Rx PharmaceuticalsJan 25, 2018 - Use cautionFood
Coblentz Distributing Inc dba Walnut Creek Foods recalls WALNUT CREEK FOODS Caramel Popcorn NET WT 15 OZ (425g) Ingredients: Evaporated Can Juice, Popcorn, Butter (cream,
Walnut Creek Foods recalls 15 oz Caramel Popcorn because soy lecithin was not listed on the label, posing a risk to those with soy allergies.
Walnut Creek FoodsJan 25, 2018 - Lower riskFood
General Mills, Inc recalls Larabar Chocolate Chip Cookie Dough, 5 - 1.6 oz (45g) bars Net Wt 8.0 oz(226g), UPC 21908-48817. Case UPC
General Mills recalls Larabar Chocolate Chip Cookie Dough bars that may contain coconut cream pie bars. Consumers should check UPC 21908-48817 for affected products.
LarabarJan 25, 2018 - Stop using nowConsumer product
VTech Recalls Lights & Lullabies Travel Mobiles Due to Injury Hazard
VTech recalls Lights & Lullabies travel mobiles due to a clamp that can break and fall. Stop using immediately for a refund or replacement.
VTechJan 25, 2018 - Stop using nowConsumer product
VTech Recalls Infant Rattles Due to Choking Hazard
VTech recalls Shake & Sing Elephant Rattles (model 80-18480: purple elephant with yellow/blue ears) due to choking hazard from breakable ears. Consumers must stop using and get refund/credit.
VTechJan 25, 2018 - Stop using nowConsumer product
Rockler Recalls Murphy Bed Kits Due to Tip-Over and Entrapment Hazards (Recall Alert)
Rockler recalls I-Semble Murphy bed hardware kits due to tip-over and entrapment hazards. Stop using immediately and contact Rockler for a free repair kit.
RocklerJan 25, 2018 - Stop using nowConsumer product
Elkay Recalls Water Coolers and Bottle Filling Stations Due to Shock Hazard
Elkay recalls water coolers and bottle filling stations with model numbers starting 1704-1706 due to risk of electric shock from loose grounding wires. Consumers must stop using immediately and contact for free repair.
ElkayJan 25, 2018 - Stop using nowMeat & poultry
Rich Products Corporation Recalls Beef Products due to Possible Listeria Contamination
Rich Products Corporation recalls 3,420 pounds of beef meatballs that may contain Listeria monocytogenes. Consumers are urged not to eat these products due to risk of serious infection, especially for pregnant women, older adults, and those with weakened immune systems.
Rich ProductsJan 24, 2018 - Lower riskMeat & poultry
FSIS Issues Public Health Alert for Chicken and Pork Products Produced without the Benefit of Inspection
FSIS public health alert: Carnival Brands produced chicken and pork products without federal inspection. Do not consume these items; they may pose health risks. The product is no longer in commerce and past its Enjoy by dates.
Carnival BrandsJan 24, 2018 - Lower riskMedical device
Fresenius Medical Care Renal Therapies Group, LLC recalls Liberty Select Cycler (SW v.2.8.7), Material Number RTLR108343 Product Usage: The device is indicated for acute and
Fresenius Medical Care is a leading global provider of renal therapies and dialysis solutions. We offer a wide range of products and services for patients with kidney disease, including hemodialysis and peritoneal dialysis solutions.
Fresenius Medical CareJan 24, 2018 - Lower riskMedical device
Keystone Dental Inc recalls Stage-1 Tissue Punch, Disposable, 4.5mm; catalog number: ISS141K. Intended for use in partially or fully edentulous
Keystone Dental recalls disposable Stage-1 Tissue Punches with potential cutting edge damage. Affected lots expire 2022-04 to 2022-07. Stop using if damaged edges cause injury.
Keystone DentalJan 24, 2018 - Lower riskMedical device
Invivo Corporation recalls DynaCad software consist of an MR Analysis Server software and the viewer workstation software. The MR Analysis
Invivo recalls DynaCad software updates 3.5 causing incorrect pharmacokinetic and diffusion maps. Users may underestimate critical medical values. No remedy stated.
InvivoJan 24, 2018 - Lower riskMedical device
Zimmer Biomet, Inc. recalls Coonrad/Morrey Elbow Implant System humeral assembly 4IN XSML, Item Number: 32-8105-027-04 (UDI: (01)0088902427
Zimmer Biomet recalls Coonrad/Morrey Elbow Implant System humeral assembly 4IN XSML (Item 32-8105-027-04) due to missing humeral bushing components. Affected units may not function properly.
Zimmer BiometJan 24, 2018 - Lower riskMedical device
LivaNova USA Inc recalls VNS Therapy Programming System, Rx Only, Model 3000, v1.0.2.2
LivaNova recalls VNS Therapy Programming System Model 3000 v1.0.2.2 due to unintended warning messages displayed on generators. Affected units have specific serial numbers and part numbers. No remedy is stated in the recall notice.
LivaNovaJan 24, 2018 - Lower riskMedical device
Mindray DS USA, Inc. dba Mindray North America recalls Hematology Diluent M-30D used with BC-3200 and BC-3600 Hematology Analyzer; Part Numbers: (1) 105-005405-00 (2 x 5.5L
Mindray recalls specific lots of M-30D hematology diluent for BC-3200/3600 analyzers that may cause elevated platelet counts in blood tests.
MindrayJan 24, 2018 - Use cautionDrug
Oxygen Development Llc recalls Life Brand Clear Action Acne Treatment Concealer Stick (Salicylic acid), 1.9g, Imported for: Shoppers Drug Mart
Life Brand Clear Action Acne Treatment Concealer Stick (1.9g) imported for Shoppers Drug Mart has failed salicylic acid stability tests after 6 months, posing a superpotent drug risk.
Life BrandJan 24, 2018 - Lower riskDrug
JCB Laboratories LLC recalls Cefuroxime, Ophthalmic Solution for Injection, 10 mg/mL, 0.3 mL single-use syringe. This is a Compounded Drug, Hospital
JCB Laboratories recalls specific ophthalmic injection solutions that may be subpotent before their 90-day beyond use date, posing a risk of ineffective treatment.
JCB LaboratoriesJan 24, 2018
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