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 1 minute ago
United StatesArrow International, LLC recalls Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: and 7 more products
Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured Due to receiving a notice from a supplier that the liquid adhesive was…LSL Healthcare Inc. recalls LSL Healthcare and 5 more products
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2110. May be… and 11 more products
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.Olympus Corporation of the Americas recalls Olympus Thunderbeat II Shears w/Ultrasonic Mode and 3 more products
Potential for detachment of a distal tip component of the device during use.Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes… and 16 more products
Unapproved design changes to the products outside of the 510(k) clearance.Medline Industries, LP recalls Medline Namic Guidewires: 1) GUIDEWIRE 3MMJ 0.035X260CM LT and 21 more products
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.Angiodynamics, Inc. recalls Soft-Vu Angiographic Catheter and 19 more products
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.Hetero Labs Limited (Unit V) recalls Pantoprazole Sodium
Discoloration: Firm received five (5) complaints stating that, "Tablets discolored darker than normal and have lighter-colored spots."Teva Pharmaceuticals USA, Inc recalls Claravis
Failed Impurities/Degradation Specifications: Out of specification for specific impurity TretinoinPremier Dental Products Co recalls Premier
Labeling: Incorrect or Missing Lot and/or Exp Date:The expiration date has an extra digit and is printed as 2709114 instead of the correct 270914 (2027-09-14).Leading Pharma, LLC recalls Furosemide Tablets
CGMP Deviations; presence of N-nitroso-Furosemide (NNF) above the recommended intake limit.B Braun Medical Inc recalls Sterile Water for Injection USP and 3 more products
Lack of Assurance of Sterility; potential for leakage from the diaphragm port once the foil is removed.Harrow Eye LLC recalls FRESHKOTE LUBRICANT EYEDROPS
Lack of Assurance of SterilityThe Harvard Drug Group LLC recalls Omega-3-Acid
Failed Capsule Specifications: Out of specification results obtained during routine stability testing for Loss on Drying of Capsule Shells.Linkbio Corp. recalls LinkBio CORE Workstation
The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.Medline Industries, LP recalls CENTURION Circumcision Kit
On lot of Sterile Circumcision Kits was distributed without the required sterilization process and is therefore not sterile.Siemens Medical Solutions USA, Inc recalls ARTIS Pheno VE30A and VE40A
During 3D acquisitions, lighter and darker patient images may be captured, which may result in less accurate 3D reconstruction.Philips Medical Systems recalls Philips Spectral CT on Rails. Model Number: 728334.
Philips has identified three software issues: 1.B Braun Medical Inc recalls B. Braun Hemodialysis Bloodlines and 5 more products
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.Clariance-SAS recalls Brand Name: Elegance¿ Anterior Cervical Plate Product Name: ELEGANCE 1 LEVEL CERVICAL…
Due to a quality issue regarding the presence of burr on the finished cervical plate product.Beta Bionics, Inc. recalls iLet Ace Pump Kit REF: BB1001 iLet Dosing Decision Software
it was found that in versions 1.3.7, 1.4.2, and 1.4.3, the Lock Screen and Limited Access Passcode Screen on the iLet graphical user interface (GUI) include certain…Philips Medical Systems Nederland B.V. recalls Philips AneurysmFlow. Model Number: 001015. AneurysmFlow is a software medical device
Potential safety issue involving the Mean Aneurysm Flow Amplitude (MAFA) ratio of AneurysmFlow (Interventional Tool).Therakos Development Limited recalls Brand Name: Cellex Photopheresis System Product Name: CELLEX Photopheresis Kit…
Increased difficulty in installing the centrifuge bowl onto the centrifuge bowl holder.A little guidance
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