Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,302 recalls, newest first · Checked 0 minutes ago
Cipla USA, Inc. recalls Fosfomycin Tromethamine Granules for Oral Solution
Failed Impurities/Degradation SpecificationsCarolina Infusion, LLC recalls TIRZEPATIDE 26 MG/ML INJECTABLE and 15 more products
Lack of Assurance of Sterility: Related to formulation using bacteriostic water; Related to processing equipment used in compounded product.K.C. Pharmaceuticals, Inc. recalls Artificial Tears Sterile Lubricant Eye Drops and 7 more products
Lack of Assurance of SterilityCareLinkâ„¢ SmartSyncâ„¢ Device Manager
An update within the Apple iPad Operating System (OS) may reduce Bluetooth disconnections between the Medtronic CareLink™ SmartSync™ (SmartSync) device manager software…Tracoe Experc Percut Dilation Tracheostomy Set W/Trachatraumatic Inserter
Tracoe is issuing a Field Safety Notice as the application bears a very low risk that the silicone sleeve may detach from the guiding catheter when removing the…Philips Allura Xper Systems
Philips has identified a software issue that may cause the Flexvision software application to become unresponsive during clinical use.Par Health Issues Voluntary Nationwide Recall of Argatroban Injection Due to the Presence of Particulate Matter
Presence of particulate matter, identified as cellulose, polystyrene, polyethylene terephthalate, stopper material, and possibly stainless steelPuella perfume safety alert: chemical risk
This product has an excessive concentration of Isoeugenol (measured value: up to 0.14% by weight).Body spray safety alert: chemical risk
The product contains hydroxyisohexyl 3-cyclohexene carboxaldehyde (HICC), which is prohibited in cosmetic products.Par Health Issues Voluntary Nationwide Recall of Two Lots of Brevital® Sodium 500 mg/vial CIV (Methohexital Sodium for Injection, USP) Due to the Presence of Particulate Matter
Presence of particulate matter identified as celluloseSchwarzkopf hair mousse safety alert: chemical risk
According to the list of ingredients, the product contains butylphenyl methylpropional (BMHCA), which is prohibited in cosmetic products.Helios Herb after sun lotion safety alert: chemical risk
According to the list of ingredients, the product contains butylphenyl methylpropional (BMHCA), which is prohibited in cosmetic products.Lotus Valley PERFUMES eau de toilette safety alert: chemical risk
According to the list of ingredients, the product contains butylphenyl methylpropional (BMHCA), which is prohibited in cosmetic products.FreeO2 Automated Oxygen Therapy Device Adult & Pediatric - Version HW 2.3
Under specific conditions following a deep battery discharge, error 29515 may occur during startup of a FreeO2 HW 2.3 device using software package 1.4.2 and prevent…TruSystem 7000 and TruSystem 7500 Surgical Tables
Baxter Corporation is issuing a voluntary correction for certain TruSystem 7000 and TruSystem 7500 surgical tables due to a reported issue with the main lift mechanism.Cardinal Health Presource Kits
Cardinal Health Presource® has identified various kits that may contain a component impacted by the welmed, extension tubing sets component.Avantage Inserter Handles and Grippers
It was identified while using the Avantage inserter handles and grippers during the implantation of the acetabular shell, that the acetabular shell may not consistently…Levantiner intimate care sponges safety alert: health risk or other risk
Although the product is accompanied by instructions on how to use, clean and store it, these contain no information on the risk of toxic shock syndrome (TSS), which can…Body spray safety alert: chemical risk
The product contains hydroxyisohexyl 3-cyclohexene carboxaldehyde (HICC), which is prohibited in cosmetic products.Karl Storz Endoscopy recalls HOPKINS Telescope 30¿
Due to incorrect inside packaging label for eyepiece.Noxbox LTD recalls NOxBOXi Nitric Oxide Delivery System. Model Number: NOXBOX-I.
Potential for irregular oxygen readings due to a manufacturing issue affecting certain oxygen sensors.Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Revised C-Reactive Protein
The potential for falsely elevated results.HeartSine Technologies Ltd recalls HeartSine samaritan PAD
Products were distributed without the required Maintenance Supplement, which describes an extra check every 3 months in addition to the monthly check.A little guidance
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