Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,304 recalls, newest first · Checked 7 minutes ago
Canada
Traditional Kohl Products recalled due to chemical hazard
The recalled products contain lead above the impurity limits outlined in the Guidance on Heavy Metal Impurities in Cosmetics.Imager™ II Angiographic Catheter
Boston Scientific is initiating removal of Imager II Angiographic Catheters (“Catheters”) due to a manufacturing issue affecting the catheter tip.LEO+ Intracranial Self Expandable Stent And Delivery System
As a precautionary measure, Balt Extrusion is voluntarily recalling specific ANRYV connector lots after routine quality control identified non-conforming bacterial…LIFEPAK ® 35 Monitor/Defibrillator
Stryker has identified an issue with the LP35 where the device does not display the message "CHECK RHYTHM / ECG Analysis Inconclusive" as intended when specific…BiCOAG Hemostasis Probe
Olympus determined that the affected products may have been manufactured without the designated amount of adhesive to the rear of the device’s ceramic tip, which may…Quantum PureFlow Standard Heat Exchanger High Flow
Blood-to-glycol leakage was identified in the heat exchanger during the procedure.
United StatesPhilips Healthcare (Suzhou) Co., Ltd. recalls Philips Incisive CT with software V4.5&V5.0
Potential of failing to trigger clinical scan during Bolus Tracking.FUJIFILM Healthcare Americas Corporation recalls FUJIFILM Synapse PACS software v7.4.310
Software issue may cause the ruler measurement to be inaccurate.Healthmark Industries Co., Inc. recalls healthmark ProChek-II and 1 more products
Test manufactured with an expired ingredient which may present as either a false negative or positive.ConMed Corporation recalls CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B…
Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.Henry Schein Inc. recalls Structur 2 SC Temporary Resin Cartridge Refill 75Gm and 1 more products
Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S.Midmark Corporation recalls Midmark IQecg Digital ECG and 1 more products
A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation.Hollister Ulc recalls Onli 17cm Hydrophilic Urethral Intermittent Catheter
Hollister has identified that select lots of the catheters identified in the above table may exhibit a protrusion caused by a manufacturing defect which might lead to…Medline Industries, LP recalls Medline medical convenience kit labeled as: TRACH TUBE KIT
Component labeling discrepancyGE Medical Systems Information Technologies Inc recalls PORTRAIT CORE SERVICES SOFTWARE V1.1 and 3 more products
Software issue may result in a loss of patient monitoring at the Hub and Central Viewer.American Contract Systems Inc recalls American Contract System Convenience Kit and 3 more products
The Convenience Kits contain Medline s Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays.AVID Medical, Inc. recalls Brand Name: Halyard Product Name: DAVINCI TRUCUSTOM BUNDLE containing TRAY FOLEY 16FR… and 1 more products
Labeling Deficiency: The medical kit labeling fails to identify that the statlock component contains natural rubber latex.Medline Industries, LP recalls Medline medical convenience kits and 3 more products
Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential…Canon Medical System, USA, INC. recalls Alphenix Models INFX-8000C INFX-8000F INFX-8000V This device is a digital…
Due to the fixing screws of ceiling movement gear in ceiling suspended arm that are part of the X-ray interventional systems may become loose.Merge Healthcare, Inc. recalls Merge PACS and Merge OrthoPACS
Software issue may cause measurements to be displayed inaccurately.Fresenius Medical Care Renal Therapies Group, LLC recalls Fresenius Medical Care
Fresenius Medical Care Renal Therapies Group, LLC (FMCRTG) has received complaints regarding flow-, no water-, or temperature-related alarms with the 2008T¿ BlueStar…Olympus Corporation of the Americas recalls POWERSEAL 5 MM
Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device.Medline Industries, LP recalls Medline Hudson RCI and 2 more products
Neonatal and infant heated wire breathing circuits may experience sporadic failure.A little guidance
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