Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,324 recalls, newest first · Checked 19 minutes ago
United StatesGetinge Disinfection Ab recalls Getinge 88-Series Washer- Disinfector. Model Number: 88-5.
Potential for device to overheat during operation if the circulation pressure calibration was not performed or had been performed incorrectly, and the low-pressure…Aesculap AG recalls AESCULAP ELAN 4 FIXED DURAGUARD STANDARD. Model Number: GB942R. and 1 more products
Mislabeling.Philips Medical Systems Nederland B.V. recalls Allura Xper FD10C and 14 more products
The BIOS battery may deplete faster than initially anticipated during the design phase.Medline Industries, LP recalls Reprocessed Livewire Steerable Electrophysiology Catheter Item Numbers 401575RH 401582RH… and 4 more products
Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates.Draeger, Inc. recalls Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software… and 1 more products
The device either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.Zap Surgical Systems recalls ZAP-X Radiosurgery System
If the radiosurgery system triggers a proximity error message during a long gantry move (greater-than180 degrees), and a subsequent proximity error message occurs after…MedicalCommunications GmbH recalls Ashvins variant HEYEX 2 / HEYEX PACS. Software Version: Version 2.6.0
Potential that the measured value may be smaller than the actual area.Northeast Scientific Inc. recalls NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy Catheter. Model Number… and 7 more products
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.North American Rescue LLC. recalls JUNCTIONAL EMERGENCY TREATMENT TOOL
Device used for unilateral or bilateral occlusion of blood flow to the lower limbs has a potential manufacturing defect that may compromise the structural integrity of…Siemens Medical Solutions USA, Inc recalls Biograph mMR. Model Number: 10433372. and 14 more products
There is a potential for an ice blockage to form or currently exist within the magnet venting system.Medtronic MiniMed, Inc. recalls Medtronic
The device cap label may not adhere to the sensor, compromising the sterility of the sensor, and increasing the risk of infection.Amerisource Health Services LLC recalls Carbamazepine Extended-Release Tablets
Failed Dissolution Specifications.Apotex Corp. recalls Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution and 1 more products
Lack of Assurance of Sterility; atypical weight loss due to improper bottle sealing leading to potential sterility concernsZydus Pharmaceuticals (USA) Inc recalls Entecavir Tablets and 1 more products
Failed impurity/degradation specifications:Out of Specification result for an individual organic impurity
CanadaFilter Set For Cook K-Mar 5200 Pumps
For the device in question and, therefore, what was imported as a Class I device, has now been determined to be a Class II device.IMRIS Systems
This recall is being initiated to address a notification received by IMRIS Imaging, Inc.Precision1 One-Day Contact Lenses
Alcon is initiating a medical device recall for lot A8041128 of its Precision1â„¢ Daily Soft Contact Lenses.Ziptight, Acute Ac Joint Implant, Single Ziploop
Zimmer Biomet is conducting a medical device recall for one lot of the Ziptight, Acute AC Joint Implant, Single Ziploop.
Various Magic BM products recalled due to missing mandatory hazard labelling
These products do not meet the Cosmetic Regulations in Canada.
United KingdomMitchum 48-hour 100ml Roll-On Antiperspirant and Deodorant safety warning
Following a manufacturing process change affecting a raw material used in select batches, there have been reports of consumers receiving adverse effects when used…Alinity HQ Analyzer
An issue has been identified in Alinity HQ Analyzer software versions 5.0 to 5.10.1.Carescapeâ„¢ Central Station
GE healthcare has identified an issue affecting Carescape™ Central Station (CSCS) with software version v3.0.5, which can cause the system to enter a continuous reboot…Endoscopy Trocar
Aesculap AG identified through investigations of complaints that the yellow sealing component of the affected reusable trocar systems 10mm and 12mm exhibits uneven…A little guidance
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