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 2 minutes ago
United StatesBecton Dickinson & Co. recalls BD EpiCenter Microbiology Data Management System and 5 more products
Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor.Theken Companies LLC recalls iNSitu Bipolar Hip System
Downstream recall for RES 97605, BioPro femoral components.Wipro GE Healthcare Private Ltd. recalls GE Healthcare Carescape Central Station and 1 more products
Carescape Central Station (CSCS), software version V3.0.5, can cause the system to enter a continuous reboot cycle.Philips Medical Systems Nederland B.V. recalls Zenition 50
Over time some systems may experience loss of imaging functionality and/or poor image quality due to potential corrosion of the Image Intensifier Television (IITV)…Tandem Diabetes Care, Inc. recalls t:slim X2 insulin pump with Interoperable Technology
A software defect in versions 7.9.0.1 and 7.10.1 of the pump software for Tandem t:slim X2 and version 7.9.0.1 of the Tandem Mobi pump with Control-IQ+ technology that…CPM Medical Consultants, LLC. recalls Fuse ULTRA Foot Plating System Instructions for Use. Models: OS200400
Instructions for use for a foot plating system is being updated to remove the second option of requirements for sterilization which was 3 minutes exposure time at…UIH Technologies LLC recalls Shanghai United Imaging Healthcare Co. and 8 more products
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.Cardinal Health 200, LLC recalls Salem Sump PVC Tubes: Product Code/Product Name: 8888264911E ENFit" SALEM SUMP" PVC TUBE… and 5 more products
Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use.Baxter Healthcare Corporation recalls Oral Probe
Affected oral/axillary probes were inadvertently programmed with the rectal probe configuration.Ge Medical Systems Israel, Functional Imaging recalls Elscint Cardial and 13 more products
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without…Sedecal Sa recalls Sedecal Mobile Digital Diagnostic X-Ray Systems and 41 more products
Sedecal sent an email to its consignees to remind the users that the equipment is not water-resistant and must be cleaned strictly according to the instructions in the…Medline Industries, LP recalls Excelsior Medical
Medline has identified a limited quantity of saline IV flush syringes that may not meet the required concentration of sodium chloride.Bristol-Myers Squibb Company recalls Opdualag
Lack of Assurance of Sterility.Aspiro Pharma Limited recalls Ketorolac Tromethamine Injection
Presence of Particulate Matter: Particulate matter identified as glassChurch & Dwight Co., Inc. recalls ZICAM" MEDICATED FRUIT DROPS ELDERBERRY FLAVOR
Labeling: Label Mix-up: The product in the bottle contains elderberry and the label failed to indicate the inclusion of elderberry as an ingredient.Medline Industries, LP recalls Medline
Subpotent DrugUSV Private Limited recalls Olopatadine Hydrochloride Ophthalmic Solution USP 0.1 %
Failed Impurities/Degradation Specifications: The result for 'Any individual unspecified impurity' exceeds the specification limit.ibspot recalls Taoscare Motion Sickness Patches 36-count box
Marketed Without an Approved NDA/ANDAJB Chemicals and Pharmaceuticals Ltd recalls Cetirizine Hydrochloride Tablets USP 10 mg and 1 more products
Tablet/Capsules Imprinted with Wrong IDThe Harvard Drug Group LLC recalls Gabapentin Capsules and 1 more products
Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .Lannett Company Inc. recalls Niacin Extended-release Tablets
Failed Dissolution SpecificationsGraviti Pharmaceuticals Private Limited recalls Bupropion Hydrochloride Extended-Release Tablets USP
Failed Tablet/Capsule SpecificationsMicrovention Inc. recalls Flow Re-Direction Endoluminal Devices: FRED 27
Flow diverter may have a manufacturing issue related to the tantalum length and/or tantalum attachment pattern, which may lead the device to be incompletely open or not…A little guidance
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