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 18 minutes ago
United StatesCooperVision, Inc. recalls Brand Name: Pearle Vision 1 day Product Name:
A small number of lenses within the affected lot are of the incorrect power.Boston Scientific Corporation recalls Imager II Angiographic Catheters M001314001 IMAGER II/5/ST/65/038 BX5
Tip may fracture or detach, leading to device fragments remaining within the patient or migrating through the vasculature.Cardinal Health 200, LLC recalls Presource Convenience Kits: 1) KIT and 1 more products
The kits contain applicators that may exhibit an open or incomplete seal on the packaging of the applicator.AVID Medical, Inc. recalls Halyard IV START KIT NON-STERILE and 1 more products
Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may exhibit an open or incomplete seal on the packaging of the applicator.Baxter Healthcare Corporation recalls PRO+ MRS SURFACE FOR VERSACARE and 2 more products
There is an error in the product description on the Unique Device Identification (UDI) label.DeRoyal Industries Inc recalls REF: 81-030415 Myocardial Probe Non-Pyrogenic
Myocardial temperature probes contain an incorrect needle.AVID Medical, Inc. recalls Halyard IV START KIT NON-STERILE
Convenience kits containing BD ChloraPrep Clear - 1 mL Applicator, which may be contaminated with Aspergillus penicillioides.New York Embroidery Studio, Inc. recalls New York Embroidery Studio Trinity Non-Surgical Isolation Gown
Gowns do not consistently meet the minimum liquid-barrier performance required.Ventec Life Systems, Inc. recalls HF2P0ST9 HomeFill Oxygen System HomeFill Cylinder M9 with CGA870 Compatible Post Valve and 2 more products
Labeling; Oxygen Cylinders do not contain required medical gas labelingHeidelberg Engineering GmbH recalls Brand Name: Heidelberg Engineering GmbH Product Name: SPECTRALIS with Flex Module…
Wheels may come loose when module is being pushed or pulled during movement or transportation, affecting stability of the stand.Medline Industries, LP recalls Medline Convenience Kits: 1) PEDS SINUS PACK and 4 more products
The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels.Olympus Corporation of the Americas recalls Olympus EZDilate Endoscopic Balloon Dilator Wired-guided 11
Potential for the inflation chart label affixed to the shaft of the device to be incorrect and indicate a balloon diameter of 18, 19, or 20 mm,Intervascular, Sas recalls Cardioroot Woven Collagen Coated Vascular Graft
Product failed to meet the specified acceptance criteria for Integral Water Permeability (IWP).Biomerieux Inc recalls VITEK 2 AST-N461 TEST KIT
The issue is related to card pouch damage associated with a portion of the lot which was produced on a specific card pouching device, in a specific timeframe, causing a…Criticare Technologies, Inc. recalls nGenuity Patient Monitor with Capnography
Complaint trend where "Checkline Error" alarm presents at device setup, rendering the CO2 monitoring function inoperable.Fresenius Medical Care Renal Therapies Group, LLC recalls CombiSet Hemodialysis Blood Tubing Set with Attached Priming Set and Transducer Protectors
Communication to recommend reviewing the IFU and ensuring that all treatment preparation and handling steps are performed as instructed.CooperSurgical, Inc. recalls INCA and 1 more products
Potential to exhibit a loose connection between the flexible tubing and the nasal cannula, during assembly or while in use, which may result in loss of CPAP pressure…Abiomed, Inc. recalls Automated Impella Controller
Retrospective report of issues remedied in 2019 with firmware and software patches: 1.Philips North America Llc recalls Achieva 1.5T and 11 more products
A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that reconstruction…Midmark Corporation recalls Midmark IQvitals Zone and 3 more products
A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.Medline Industries, LP recalls Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK…
Kits contain Healthmark Instrument Channel Brushes, which were recalled by the manufacturer due to the potential for a sharp edge/burr on the end of the brush.Olympus Corporation of the Americas recalls Olympus BiCOAG Hemostasis Probe 10Fr Coaxial Connector. Model/Catalog Number: CD-B610LA. and 3 more products
Potential for detachment of ceramic tip due to manufacturing without the designated amount of adhesive.SHANTOU Qiwei industrial Co., Ltd recalls MENOW SUNSCREEN PRESSED POWDER SPF35 PA+++
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