Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,324 recalls, newest first · Checked 3 minutes ago
United KingdomNoor Gold Beauty Cream safety warning
The product presents a serious chemical risk as when tested, the cream was found to contain 27250mg/kg (2.72%) mercury.Sandal Whitening Beauty Cream safety warning
The product presents a serious chemical risk as when tested, the cream was found to contain 14860mg/kg (1.49%) mercury.B&M Cream and Green Mug recall
The product presents a risk of burns as the base may crack and break when filled with hot liquid.
CanadaImportant Safety Information on Yescarta (axicabtagene ciloleucel) and the Risk of Cerebral Edema in Primary Mediastinal B Cell Lymphoma (PMBCL)
Patients being treated with Yescarta for primary mediastinal B-cell lymphoma (PMBCL) may be at increased risk for developing cerebral edema, including fatal events…Beckman Coulter AU Immunochemistry System- HDL/LDL Cholesterol Assay
LDL cholesterol OSR6x96 does not meet the triglyceride interference claim per the BAOSR6x96 v10 IFU which states "no significant interference up to 1,500 mg/dl…Vanta/Sequentia Lt Clinician Programmer Application
The Vanta A71200 CP app V2.0.2465 and V2.0.2683 will display a "system error" if the user selects the start usage button twice when interrogating a new implantable…
United StatesAccriva Diagnostics, Inc. recalls Hemochron Activated Clotting Time Low-Range Test Cuvette
Test cuvettes, used with an assay for monitoring heparin anticoagulation, may have a foreign object that has sharp edges and could pose a risk of injury if not detected…Illumina, Inc. recalls Reagent Kits/ containing flow cells
An instrument intended for sequencing DNA libraries with in vitro diagnostic assays is used with reagent kits including flow cells that have flow cell gaskets that have…Enterix, Inc. recalls InSure ONE Fecal Immunochemical Test. Labeled as follows: 1. Insure ONE POL Patient Kit
InSure ONE failed sensitivity testing when used with Test Card Lot T241102, which may result in false negative results.Medtronic, Inc. recalls Aurora EV-ICD and Clinical EV-ICD
There is a potential for delayed time to high-voltage (HV) therapy should a rare sequence of events occur.Aizu Olympus Co., Ltd. recalls Olympus OER-Elite and 2 more products
Inform existing affected device customers about pertinent Warnings/Cautions, existing recommended maintenance schedules and that only properly trained personnel conduct…Fresenius Kabi USA, LLC recalls IVENIX INFUSION SYSTEM
Incorrect assembly of specific lot of LVP Primary Administration Set that could result in serious patient injury.Microbiologics Inc recalls KWIK-STIK
Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.Siemens Medical Solutions USA, Inc recalls MAMMOMAT Revelation and 2 more products
There were instances where the operator table was sold together with a bus-installation kit.Paragon 28, Inc. recalls Phantom Fibula Nail
Fibula nail system intended for use in fixation of fibular fractures and osteotomies, has out of specification thread depths on the fibula nail, so implant may not be…Philips North America Llc recalls Incisive CT and 1 more products
If the screws of tube heat exchanger on the rotating scanner are not tightened well after replacing.Fresenius Kabi USA, LLC recalls Ivenix Infusion System
Downstream Occlusion alarms may occur during procedures using low flow infusion rates when a check valve* is added to the Ivenix Administration Set.Baxter Healthcare Corporation recalls Welch Allyn INF BAG
Replacement bladder kit for the Welch Allyn two-piece reusable blood pressure cuff may contain a Large Adult size bladder rather than a Thigh size bladder in the…Philips Ultrasound, LLC recalls Lumify Diagnostic Ultrasound System models : 795005
Ultrasound system compatibility issues with Apple devices running iOS 18 may cause a failure to perform live imagining.Get Tested International Ab recalls Alcohol and 87 more products
Distribution without premarket approval/clearance.Philips North America Llc recalls IntelliVue MP2. Product Number: M8102A. and 21 more products
Potential issue where the IntelliVue monitors did not alarm.Cipla Limited recalls Phytonadione Injectable Emulsion
Failed Stability Specifications: Observed OOS results: eg results for colour indexTeva Pharmaceuticals USA, Inc recalls Carton label: Testosterone Gel 1%
Defective Container - A defect in the side-seal which allows leakage of product.A little guidance
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