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 4 minutes ago
United StatesMedicalCommunications GmbH recalls Ashvins variant HEYEX 2 / HEYEX PACS. Software Version: Version 2.6.0
Potential that the measured value may be smaller than the actual area.Northeast Scientific Inc. recalls NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number… and 7 more products
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.North American Rescue LLC. recalls JUNCTIONAL EMERGENCY TREATMENT TOOL
Device used for unilateral or bilateral occlusion of blood flow to the lower limbs has a potential manufacturing defect that may compromise the structural integrity of…Siemens Medical Solutions USA, Inc recalls Biograph mMR. Model Number: 10433372. and 14 more products
There is a potential for an ice blockage to form or currently exist within the magnet venting system.Medtronic MiniMed, Inc. recalls Medtronic
The device cap label may not adhere to the sensor, compromising the sterility of the sensor, and increasing the risk of infection.Amerisource Health Services LLC recalls Carbamazepine Extended-Release Tablets
Failed Dissolution Specifications.Apotex Corp. recalls Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution and 1 more products
Lack of Assurance of Sterility; atypical weight loss due to improper bottle sealing leading to potential sterility concernsZydus Pharmaceuticals (USA) Inc recalls Entecavir Tablets and 1 more products
Failed impurity/degradation specifications:Out of Specification result for an individual organic impurityEthicon, LLC recalls STRATAFIX Spiral PDS Plus Bidirectional Knotless Tissue Control Device
Potential for barb non-engagement.Boston Scientific Corporation recalls Extractor Pro RX Retrieval Balloon Catheter
The product in incorrectly labeled.Mindray DS USA, Inc. dba Mindray North America recalls BeneVision N1 Patient Monitor
Potential for activation of an abnormal alarm pause.Biofire Defense recalls FilmArray NGDS Warrior Panel NGDS-ASY-0007 is a qualitative
FilmArray NGDS Warrior Panel (NGDS-ASY-0007) has an increased risk of internal control failures when testing positive blood culture, which may lead to delayed results…Biomet, Inc. recalls Juggerknot Mini Soft Anchors
The outer carton box label is for the JuggerKnot 1.0mm Mini products.CooperVision, Inc. recalls MyDay Toric and 2 more products
One lot manufactured with an invalid sterilization cycle.Ortoma Ab recalls Ortoma Inserter Adapter OTD: Inserter Adapter OTD Straight REF 30-201 Model Number: 2001…
Due to a weld breakage between the pin and inserter holder of the Inserter Adapter.Philips North America Llc recalls Philips CT systems labeled as the following: 1. Brilliance CT 40 Channel and 9 more products
The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.Stryker Communications recalls Chromophare Surgical Light System
Surgical lights have stress lines forming on the powder coating, which indicates that powder coating chipping can occur.Abiomed, Inc. recalls Automated Impella Controller
Specific Automated Impella Controllers (AICs) that have a Pump Driver Circuit Assembly do not meet current specifications.Maquet Cardiovascular, LLC recalls Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000. The VASOVIEW…
Reports of out-of-box failures discovered during the limited launch phase.MEDLINE INDUSTRIES, LP - Northfield recalls Medline medical convenience kits labeled as: 1. ADULT INTUBATION TRAY and 1 more products
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles due to…Philips Medical Systems Nederland B.V. recalls Allura Xper FD10 Product Codes: and 12 more products
Systems may not perform as intended due to the deterioration of certain internal components (the CMOS battery, hard disk drive, and/or power supply unit).Tandem Diabetes Care, Inc. recalls t:slim X2 Insulin Pump with Interoperable Technology
an app defect that occurs when the phone is set to a right-to-left language, which causes app-pump pairing issues and graphical defects, which can potentially lead to…Baxter Healthcare Corporation recalls Baster Continu-Flo Solution Set
Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for one lot of Continu-Flo solution sets listed below due to customer reports of tubing…A little guidance
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