Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,315 recalls, newest first · Checked 0 minutes ago
CanadaSAFE-T-FILL®
The SAFE-T-FILL® blood collection devices and accessories are being recalled due to (i) potential of falsely elevated blood lead levels when used in conjunction with…Ventilator Circuit For Non-Invasive Ventilation
Armstrong Medical LTD are submitted this FSCA report in relation to the recall and field safety notice for a device correction to mitigate the risk of tubing separation…
Truly Tallow All-in-1 Mens Face + Body + Hair Whipped Tallow recalled due to a 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…VITEK® 2 Systems
BioMérieux identified increased out-of-range high quality control results for the following antibiotic formulations: ceftazidime/avibactam (CZA02n), imipenem (IPM05n)…
United StatesC-Rad Positioning Ab recalls Brand Name: Catalyst+ Product Name: Catalyst
Due to issues with the system's stereotactic radiosurgery (SRS) treatment cannot be guaranteed for all couch angles and system setups.Boston Scientific Corporation recalls Boston Scientific Coyote OVER-THE-WIRE PTA Balloon Dilation Catheter
Boston Scientific is initiating the removal of certain batches of Coyote" Over-the-Wire (OTW) Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter…Medtronic Inc recalls Abre Venous Self-Expanding Stent System
Stents may be impacted by a Nitinol anomaly which causes a reduced stent diameter when deployed and corresponding reduced radial force.ICU Medical, Inc. recalls Plum Duo Infusion System
ICU Medical received one lot of defective primary speakers from our supplier that may fail to produce an audible sound.Thoratec LLC recalls CentriMag Blood Pump
Acute circulatory support system pump may not fit into the motor and reports received of the pump not being securely locked into the motor using the screw-in locking…Instrumentation Laboratory recalls The product is used for the evaluation of the intrinsic coagulation pathway
Potential for microbial contamination.Fresenius Kabi USA, LLC recalls Ivenix Infusion System
Emphasizing instructions for LVP duration programming located in the IFU.Philips Medical Systems Nederland B.V. recalls Philips Azurion Systems with software versions R2.1.10 and R2.2.10. Includes the…
Six (6) identified software issues which may result in the following: system keeps restarting, AMC triple drive, C-Partition of Suite PC running out of free space…Ge Medical Systems Israel, Functional Imaging recalls SMV DSX New Line and 3 more products
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and listed in…Hologic, Inc recalls ThinPrep¿ CytoLyt¿ Solution. Buffered Cell Wash Solution.
Fungal contamination of affected lot with Parengyodontium album.Abbott Diabetes Care, Inc. recalls FreeStyle Libre 3 Sensor REF 72081-01 UDI-DI code: 00357599818005 The FreeStyle Libre 3… and 3 more products
Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose resultsDiagnostica Stago, Inc. recalls Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is intended for…
Potential for defect for Asserachrom HPIA lot 271288, which can affect every well in the impacted strip and produce negative results.ICU Medical Inc. recalls Pulsator Arterial Blood Sampling Kit and 1 more products
Affected lots of syringes may have a crack on the syringe collar, which may lead to delayed or repeated blood draw/fluid delivery.Repligen Corporation recalls MAVERICK¿ Measurement Module Spectrometer PN 820-01367
Potential Elevated Laser Output A disconnected cable or a poorly crimped cable under mechanical bending stress can cause loss of electrical contact.Mobius Imaging, LLC recalls Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Tomography and 1 more products
AIRO pendant replacement kits and upgrade do not possess the "Safe Hand Position Warning" label.Philips Medical Systems Nederland B.V. recalls Philips Azurion Systems R3.0. Includes the following label descriptions and…
Nine (9) identified software issues which may result in the following: loss of X-ray after Pedal Tap, loss of X-ray after Phase Fault, missing live X-ray on the…Medicrea International recalls Medicrea and 1 more products
Due to complaints, orthopedic rotation tool handle may untread from the shaft resulting in the inability to rotate implant.Medtronic Neuromodulation recalls A71200 Vanta" Clinician Programmer Application
Complaints received that Vanta A71200 CP App does not function as intended during use.Heraeus Medical GmbH (Dental Division) recalls Brand Name: PALACOS Product Name: PALACOS R pro 40 and 3 more products
increase of complaints regarding the breakage of the ampoules within their device systems.A little guidance
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