Medicine, medical device and cosmetics recalls in United States
Recalls of medicines, medical devices, supplements, cosmetics and personal care products published in United States, newest first.
1,518 recalls, newest first · Checked 12 minutes ago
United StatesMerck Sharp & Dohme LLC recalls Merck Emend and 1 more products
Presence of particulate matter: potential presence of metal particulates in the product.DICOM Grid, Inc. recalls Intelerad InteleShare software
Software intended to aid in diagnosing conditions, planning treatments, visualizing anatomical structures has a bug that, if all of following are met: Viewing images in…Medline Industries, LP recalls SCISSORS and 1 more products
The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.Medtronic MiniMed, Inc. recalls InPen App
When app is uninstalled and reinstalled, insulin pen software issue causes Choose Notification Style Screen to not show during setup so users can't choose to allow…Seaspine Orthopedics Corporation recalls Orthofix NorthStar OCT Navigation Surgical Technique Guide
The NorthStar OCT Navigation Surgical Technique Guide (STG) incorrectly identified both Medtronic s Solera and Medtronic s Infinity system toolcards as compatible with…Copan Italia recalls 1ml of DTT in liquid phase and 1 more products
Treatment reagent functionality in respiratory specimens liquification cannot be guaranteed.Fresenius Medical Care Holdings, Inc. recalls 5008X CAREsystem +CLiC +CDX
Several software anomalies with the potential to impact patient treatment, of which one includes the possibility to result in treatment stop if certain conditions are…Fresenius Kabi USA, LLC recalls Ivenix Infusion System
Software version 5.10.1 and earlier contain anomalies that have the potential to cause serious patient harm or death.Dsaart LLC recalls Brand Name: AART Silicone Carving Implant Product Name: Silicone Carving Implant… and 5 more products
Due to manufactured products that deviated from established specifications and being distributed without obtaining the required FDA premarket approvals or clearances.GE Medical Systems China Co., Ltd. recalls GE Healthcare Carestation anesthesia system and 2 more products
Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is unplugged or in…Datascope Corp. recalls Cardiosave Hybrid and 1 more products
The IFU addendum updates the Vibration and Shock Table to reference the correct standards.GE Healthcare GmbH recalls GE HealthCare ViewPoint 6
GE HealthCare has become aware that the Patient History tab in ViewPoint 6 versions 6.15.3 and 6.15.4 ultrasound software may not include complete patient medical…Rocket Medical Plc recalls Brand Name: Rocket Product Name: Rocket 12Fg Seldinger Catheter Procedure Tray… and 5 more products
IFU and device kit labeling contains misleading statements leading to improper securing of the device resulting in the potential to fall out during use.AVID Medical, Inc. recalls Halyard and 4 more products
Potential for incomplete seal on header bag.Abbott Laboratories recalls Alinity ci-series System Control Module
Abbott Laboratories is recalling their Alinity ci-series System Control Module, a chemistry/immunoassay anayzer, by correction.Myofunctional Research Company USA recalls Myosa for Kids KS1 REF MyOSAKS1_Sb/Sp/Mb/Mp/Lb/Lc KS2 REF MyOSAKS2_Sb/Sc/Mb/Mc/Mp/Lb/Lc…
Due to firm mistakenly distributing product within the U.S.Path recalls MADSEN ACCUSCREEN TEOAE/DPOAE/ABR Probe
Following a component change in the DPOAE probe (speaker replacement), technical distortions may occur at high stimulus levels combined with unusually low OAE amplitude…Mindray DS USA, Inc. dba Mindray North America recalls Hardware configuration of the BeneVision Central Monitoring System
When the Worstation of the BeneVision DMS has a specific hardware configuration, the computer may experience audio playback failure or screen freezing.Zimmer Surgical Inc recalls Zimmer Air Dermatome and 1 more products
The devices may have a misaligned thickness control bar.Instrumentation Laboratory recalls HemosIL SynthAFax. Partial Thromboplastin Time Tests.
Recalled lots were manufactured with double the amount of preservative concentration.Smith & Nephew, Inc. recalls BIOSURE HA SCREW
Removal of affected lot of screws due to labeling error.Cepheid recalls Brand Name: Xpert¿ BCR-ABL Ultra Model/Catalog Number: GXBCRABL-US-10 and 1 more products
Invitro diagnostic test kits with specimens that have elevated white blood cell count (>30,000 cell) may cause inaccurate results.Preferred Pharmaceuticals, Inc. recalls Ondansetron ODT Tablets
Defective container: Preferred Pharmaceuticals received a letter from the manufacturer Glenmark, that the blister packs are not fully sealed and tablets falling out.A little guidance
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