Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,315 recalls, newest first · Checked 17 minutes ago
CanadaVariax 2 Locking Screw - Non-Sterile
Stryker has confirmed that one lot of Variax® 2 Locking crews was manufactured without the hexalobular feature required for mating with the associated screwdriver.ALECENSARO (alectinib) and the Risk of Severe Hypertriglyceridemia
Hypertriglyceridemia, including severe and life-threatening events, has been identified as an adverse reaction associated with ALECENSARO.
United StatesLinkbio 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.Wilson-Cook Medical Inc. recalls Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only
Due to increased in complaints their is the potential for endoscopic clipping device to malfunction.Integra LifeSciences Corp. (NeuroSciences) recalls Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505. and 4 more products
Increased rate of out-of-specification endotoxin results.Gentuity, LLC recalls Gentuity HF-OCT Imaging System Model G10-01
The potential for repeated frames during HF-OCT pullback when using the Gentuity HF-OCT Console (software version 21.11 to 23.3.13) with the Vis-Rx and Vis-Rx Prime…Remel, Inc recalls Yeastone Broth
Products may report incorrect AST results during quality control.Insulet Corporation recalls Omnipod 5 Pods. Model/Catalog number: PT-001662 ASM 5PK Pod STRL OPS G6G7
Due to a manufacturing defect, certain Omnipod 5 Pods from 49 lots have an internal soft cannula tear that results in insulin leaking into the Pod instead of being…ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Arjo Tenor mobile passive patient lift
An internal component of the actuators in a certain production batch may not meet the required mechanical strength.3B Medical, Inc. recalls React Health PHOENIX 5L Oxygen Concentrator
Devices which did not meet internal quality specifications were inadvertently distributed.Island Kinetics, Inc. d.b.a. CoValence Laboratories recalls Blemish Spot Treatment
Failed Stability SpecificationsAvantor Performance Materials LLC recalls Magnesium Chloride
Subpotent drugHuons Co., Ltd. recalls Lidocaine HCl injection and 3 more products
Lack of Assurance of SterilityThe Harvard Drug Group LLC recalls Memantine Hydrochloride Extended-Release
Failed Dissolution SpecificationsNephron SC, LLC recalls Albuterol Sulfate Inhalation Solution
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