Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,312 recalls, newest first · Checked 5 minutes ago
CanadaHybrid Hydrophilic Microguidewire
Performance variability affecting the hydrophilic coating of Hybrid007 guidewires in specific lots may increase friction during microcatheter navigation.DLP Select 3D Arterial Cannula and DLP Elongated One Piece Arterial Cannulae
Beginning in April 2026, complaints were received regarding pinhole leaks in the wire-wound body of 22 Fr EOPA™ elongated one piece arterial cannulae and EOPA 3D™…Omni-Tract Surgical Retractor System
Integra Lifesciences is issuing a correction to the Integra® Omni-Tract® Surgical Retractor System - existing Instructions For Use (IFU) related to prevacuum…NephroMax High Pressure Nephrostomy Balloon Catheter
Boston Scientific is notifying you that the renal sheath for certain NephroMax™ high pressure nephrostomy balloon catheters may be packaged in a reversed orientation.Fludeoxyglucose (18F) Injection; Cracked vial
Fludeoxyglucose (18F) vial containing 24.80 mL (30.23 GBq of the product) used to administered the drug to the patients was found to be broken at the bottom.LIFECODES LSA Class II
Werfen has identified that two beads within the LIFECODES LSA class II assay kit(s) may present different DQB1 specificities than previously understood: • Bead 42 /…WASPLab
Copan WASP SRL is performing a medical device product correction related to the WASPLab product.Glidesheath Slender® Introducer Sheath
Through post-market surveillance, we have received complaints for the guidewire not being able to pass through the needle.AirSeal Access Port With Blunt Obturator and AirSeal Access Port With Optical Obturator
Complaint review identified a prior manufacturing process update that may cause erroneous overpressure alerts under certain conditions, potentially leading to loss of…RAPIDLab® 348EX System
Siemens Healthcare is informing affected customers that a software-related behavior identified in the RAPIDLab® 348EX System associated with the calcium ion…
United StatesPhilips North America Llc recalls Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the following…
Potential for device reset to default "NEW_DEVICE" state, which may lead to a to loss of device configuration and the equipment label, resulting in a failure to…Acumed LLC recalls Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe…
Due to manufacturing error, hexalobe screws used with wrist fixation system may break during use.TMJ Solutions Inc recalls TMJ Bilateral Implants
Custom temporomandibular joint implant may have contained incorrect patient-specific components that led to a poor fit of the implant, leading to a right-sided open bite.GE Medical Systems SCS recalls GE Healthcare AW Server 3.2 ext.6.5
GE HealthCare has become aware of a context synchronization issue in AW Server 3.2 ext.PFM Medical Inc. recalls Multi-Snare Set: 5 mm x 125 cm
A snare catheter including luer lock, indicated for removal or manipulation of a foreign body in the vascular system, failed to meet the biocompatibility requirements…Medline Industries, LP recalls Medline Convenience Kits: 1) DYNJ905503F and 3 more products
The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose Injection, USP…Zimmer, Inc. recalls Brand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿ Femoral…
Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package.IPG Medical Corporation recalls Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.
Software anomaly that causes a false display of error code 5018.Boston Scientific Corporation recalls Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump
There is the potential for leakage along the drug pathway from the pump through the end of the catheter.Intuitive Surgical, Inc. recalls Da Vinci ASSY
Operative components of surgical systems potentially distributed with E-brake retainer pin, so in event of a structural column failure, the E-brake pin would prevent…Stryker Neurovascular recalls INZONE DETACHMENT SYSTEM
Embolization coil detachment system devices may experience premature battery drain causing devices to: 1) Not power on; 2) Power on with faint audible and visual…Medtronic Perfusion Systems recalls Octopus Evolution Tissue Stabilizer and 2 more products
During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned.Philips North America Llc recalls Philips Avalon Fetal Monitor and 1 more products
Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent…A little guidance
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