Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,315 recalls, newest first · Checked 24 minutes ago
CanadaMedihoney® Wound and Burn Products
Sterile products: During an investigation, packaging failures were identified related to the Medihoney® wound & burn products, which could lead to a breach in the…Medline Kits containing Surgical Gowns, Packs and Drapes
Medline identified calibration issues linked to the equipment used to sterilize the recalled products, impacting the sterility assurance level.
United StatesIntuitive Surgical, Inc. recalls Brand Name: Da Vinci Product Name: da Vinci X
Due to a software implementation error that allowed instruments arms failing an important diagnostic test to remain in clinical use.Wilson-Cook Medical Inc. recalls Product Name: Nasal Jejunal Feeding Tube REF: NJFT-10
Nasal feeding tube packaged without the nasal transfer tube component.Maquet Cardiopulmonary Gmbh recalls Bubble Sensor for 3/8" x 3/32" tubing
Internal investigations have identified an issue with the durability of the connecting cable near the connection to the Venous Bubble Sensor.Beckman Coulter, Inc. recalls CellMek SPS Sample Preparation System
Sample preparation system designed to automate staining, lysing, cell washing has a software error that causes samples to be dispensed close to or touching tube…Tornier, Inc recalls TORNIER PERFORM REVERSED PERIP SCREW 5.0MMX18MM NON STERILE
A specific lot of screws is incorrectly labeled.Medtronic MiniMed, Inc. recalls MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software Version 6.60…
A software timing and processor communication issue in MiniMed" 780G software version 6.60 may trigger Pump Error 43 and/or Pump Error 41, resulting in suspension of…Olympus Corporation of the Americas recalls Brand Name: Single Use Electrosurgical Knife Product Name: Olympus Single Use… and 1 more products
A deterioration of the cutting knife, including overheating and burning, can contribute to tip breakage during use.Encore Medical, LP recalls EMPOWR 3D Knee Tibial Insert 5R 14MM and 1 more products
942-01-40G acetabular system package was found to contain 942-01-36H acetabular system; and several other acetabular system and knee insert devices may also have a…Siemens Medical Solutions USA, Inc recalls SOMATOM X.ceed Software applications: syngo.CT Brain Quantification syngo.CT Vessel… and 3 more products
To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance.FUJIFILM Healthcare Americas Corporation recalls FDR Visionary Suite
It was found that the contacts of the electromagnetic contactors used inside the cabinet of the X-ray high-voltage generator were welded, and the current might continue…Focalyx Technologies, LLC. recalls Focalyx Fusion
Software device that is an accessory for image-guided interventional and diagnostic procedures involving prostate has accessories that may not function properly with…Vantive US Healthcare LLC recalls PRISMAFLEX ST100 SET US and 7 more products
There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.Boston Scientific Corporation recalls AXIOS Stent and Electrocautery-Enhanced Delivery System and 5 more products
Increased reports of stent deployment and expansion issues.Biomerieux Inc recalls VITEK 2 Gram-negative Susceptibility Cards Containing o Polymyxin B
Potential risk of Quality Control failures and/or false resistant antibiotic results when testing isolates of Enterobacterales/Enterobacteriaceae species and/or…Changchun Wancheng Bio-Electron Co., Ltd. recalls LotFancy Urinary Tract Infection Urine and 10 more products
Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S.Etac A/S recalls Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number: and 3 more products
A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke.Fujirebio Diagnostics, Inc. recalls Product Name: Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio Model/Catalog Number… and 6 more products
Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when…Olympus Corporation of the Americas recalls Brand Name: CleverCut Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog… and 29 more products
Devices which did not undergo thermoforming could deform and lose performance.Beckman Coulter, Inc. recalls COULTER DxH Diluent
Due to specific lots of diluents contributing to elevated platelet Daily Checks background counts cycle with use with analyzers.Vortex Surgical Inc. recalls Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens and 12 more products
There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots.Handelnine Global LLC recalls Rheumacare capsules
CGMP Deviations: product found to contain lead.A little guidance
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