Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,324 recalls, newest first · Checked 1 minute ago
Canada
United StatesMicrovention 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…Contego Medical LLC recalls Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon System with Integrated…
Carotid stent and post-dilation balloon system with integrated embolic protection system has an integrated filter that may not open or may not fully open during sheath…Medline Industries, LP recalls Medline Adult Anesthesia Set
Specific items and lots of Medline Kits may contain Clearlink IV Sets which Baxter recalled due to customer reports of leaking.ConvaTec, Inc recalls DuoDERM" Extra Thin dressings are highly flexible
Wound dressing may have foreign matter on the product.Lutronic Corporation recalls XERF EFFECTOR 60. Electrosurgical unit.
Manufacturing defects in devices manufactured from 4/1/25 to 8/20/25 can on rare occasions result in adverse events for patients.Insulet Corporation recalls The failure occurs if a user on the Omnipod 5 iOS application selects and holds down on…
The failure occurs if a user on the Omnipod 5 iOS application selects and holds down on a manual entry field, to magnify the visual field using the magnifying feature…Fisher & Paykel Healthcare, Ltd. recalls Airvo 2
When unintentionally disconnected from power source, humidifier device (used to deliver high flow warmed and humidified respiratory gases) may sound audible alert for…Cook Medical Incorporated recalls Zenith Alpha 2 Thoracic Endovascular Graft
Affected devices may contain PTFE coating scrapings.Iantrek Inc. recalls Cyclopen Microinterventional Cyclodialysis System. Model Number: CP-300. Product… and 1 more products
Potential for compromised integrity of the sterile packaging.Kico Knee Innovation Company recalls Brand Name: ARVIS Product Name: ARVIS" Shoulder Model/Catalog Number: IN-27300
Complaint identified issue with AI surgical planning software that may result in implant malalignment and/or decrease range of motion.Spacelabs Healthcare, Inc. recalls Brand Name: Branding is not applied to this product. Product Name: DVI display cables… and 2 more products
Due to display cables used for monitors were not in compliance with electromagnetic interference from inadequately shielded cables which may pose serious risk to…Diagnostica Stago, Inc. recalls Product: STA Liatest D-Di
A potential risk of underestimation of D-Dimer (D-Di) levels with the two listed lots.Percussionaire Corporation recalls Phasitron 5
IFU update; in-line valve, with pressure relief seal may leak when used with ventilator; don't use in neonates/infants, with target tidal volumes less-than50mL or…Philips North America recalls Cardiac Workstation 5000 and 1 more products
Failure of Environmental Stress Testing from a pinched power module wire within the housing of the Cardiac Workstation device which resulted in a short.Ethicon Endo-Surgery Inc recalls ECHELON LINEAR Cutters Reload 80 mm Blue
The devices were shipped unsterilized.BioPro, Inc. recalls BioPro Femoral Head and 5 more products
Potential packaging issue that could compromise the sterile barrier.Boston Scientific Corporation recalls TENACIO Pump with InhibiZone and 6 more products
The potential for devices to experience inflation and/or deflation performance issues or difficulties.Ferno-Washington Inc recalls FERNO POWER X2 POWERED AMBULANCE COT
The fastening post hardware could loosen allowing the fastening post to detach from the cotAbbott recalls TactiFlex Sensor Enabled Ablation Catheter and 4 more products
Abbott has become aware of a limited number of tip detachment events during catheter removal from the packaging.GE Medical Systems, LLC recalls LOGIQ P10 series with software version R4.5.7 Model Number 5877534 and 2 more products
The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis.American Contract Systems Inc. recalls Basic Biopsy Tray and 17 more products
Identified products were re-gassed (sterilized more than once) after a nonconformance occurred during the initial Ethylene Oxide (EO) gas injection process.Olympus Corporation of the Americas recalls BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T150 and 22 more products
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and…Boston Scientific Corporation recalls ACCOLADE SR SL and 26 more products
Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state…A little guidance
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