Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,315 recalls, newest first · Checked 3 minutes ago
United StatesWizcure Pharmaa Private Limited recalls Vista Tears Polyethylene Glycol 400 0.4% w/v and 6 more products
Lack of Assurance of Sterility: Products have not been manufactured in conformance with current good manufacturing practices.
United KingdomGlow & Lovely Hydraglow Rose Enrich Serum Cream 50g safety warning
The product presents a serious chemical risk as the ingredients list had incorrect ingredients listed and had not specified fragrance allergens.Glow & Lovely Advanced Multi Vitamin Serum in Cream safety warning
The product presents a serious chemical risk as it contains butylphenyl methylpropional, also known as lilial or BMHCA.
CanadaFoaming shampoo with ghassoul and tea tree recalled due to chemical hazard
Health Canada's sampling and evaluation program has determined that the recalled product contains methyl eugenol above the maximum concentration in the Cosmetic…Kids Stuff Crazy Foaming Soap safety warning
The product contains butane, isobutane and propane, which are flammable gases.Burlington Medical Thyroid Shields, Vests, and Kilts
Burlington Medical is voluntarily recalling certain thyroid shield, vest, and kilt radiation protection garments.Sterile Contro-Vac Whistle Tip Suction Cath W/2 Gloves & Pop-Up Cup Vinyl
Medline has identified that a smaller open Suction Catheter (8Fr), may have been packed within the 14Fr Suction Catheter Kits.Champignons et Adaptogènes: Affected lot contains concentrations for certain ingredients that differ from the concentration on the label.
Affected lot contains concentrations for certain ingredients that differ from the concentration on the label.Paradigm and MiniMed 600 and 700 series pumps
As part of the testing for the Alternate Controller Enabled (ACE) device submission, the R&D team tested the Minimed 780g Insulin Pump at elevated and lowered height…Smartmix Tips Combi
The recall must be done due to misclassification which led to the sale of unlicensed medical devices.
Tubby Tots Fizzy Flash Bath Magic recalled due to injury and impact hazard
When the plastic container is opened, pieces of the bath bomb potions may be ejected and impact the consumer.Automated Impella Controller
Abiomed has identified that Automated Impella Controller (AICS) with software V8.2.3, when used in conjunction with an Impella 5.5 with smart assist set (product code…Vicks Sinus Steam Inhaler (Vih200cv1)
The Vicks Sinus Steam Inhaler was distributed in Canada without the required Medical Device License (MDL) under the Health Canada medical devices regulations.Centinel Spine, Inc. recalls Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number: PDSL6 Software…
Products were mislabeled as the 6mm product but included the 5 mm product.Intuitive Surgical, Inc. recalls Da Vinci 5 ASSY
An error event following the release of a software version for the surgical system that can result in loss of user interface content on an external monitor or tower…Medica Corporation recalls Medica Capillary Tubes
A systematic positive bias of up to 20% was identified across the reportable potassium range, resulting in false elevation results of patient samples when using Medica…Stryker Corporation recalls MOLLI 2 System System includes: MM1000
Due to a need to update the product labeling (Instructions for Use IFU) as a result of the magnetized surgical tools dislodging markers using during target tissue…Baxter Healthcare Corporation recalls Brand Name: Spectrum IQ Product Name: Infusion Pump Model/Catalog Number: 3570009…
Pumps were released without full testing being performed, including occlusion alarm testing.Olympus Corporation of the Americas recalls Olympus High Flow Insufflation Unit. Model Number: UHI. Used for insufflation of the… and 2 more products
Issue with software algorithm which may lead to overpressure events.Auris Health, Inc recalls MONARCH Platform
Device for bronchoscopic visualization, patient airway access has software issue: if application restarts after patient-side selection, prior to bronchoscope loading…Wilson-Cook Medical Inc. recalls Teslatome Bipolar Sphincterotomes REF: TESLA-B2535-260 Model Number: G60784 UDI-DI code…
Due to product that may contain a void in the material that separates the wire guide and cutting wire lumens, which may cause an inappropriate path of current during…Medline Industries, LP recalls Medline Industries IV Administration and Extension Sets: 1) DBD-IV ADMIN SET
Under circumstances involving exposure to particular chemicals and mechanical forces, the male luer connectors for the specified IV Administration and Extension sets…Olympus Corporation of the Americas recalls Olympus Thunderbeat 5 mm and 11 more products
Firm is initiating a removal due to continued reports of adverse events.A little guidance
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