Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,315 recalls, newest first · Checked 4 minutes ago
CanadaMedtronic DLP Retrograde Cardioplegia Cannulae
On 8-January-2026, Medtronic received a complaint from the U.S.Visian® ICL™/TICL™ Online Calculation Software
Between April 13 and 16, 2026, the Visian® ICL™/TICL™ online calculation software may have generated incorrect Implant Orientation Diagram (IOD) printouts used for…HydroMARK™ Breast Biopsy Site Marker
Devicor Medical Products, Inc.Vivo 45 LS
In devices with the affected firmware versions, treatment in volume-controlled ventilation modes (VCV, VCV-SIMV and VCV-MPV) can, under specific trigger conditions…Medline Convenience Kits Containing Select Polycarbonate Colored Syringes
Specific item(s) and lot(s) of Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes are recalled, after identifying unapproved design…Abbott's Proclaim™ SCS/Proclaim™ DRG/Infinity™ DBS Implantable Pulse Generators
Abbott is sharing important information regarding the Infinity™ Deep Brain Stimulation (DBS) Neurostimulation System, Proclaim™ Spinal Cord Stimulation (SCS) and…Monnal™ T60 Advanced
Air Liquide Medical Systems has identified a manufacturing non-conformity that affects a limited and specific number of Monnal T60 and Monnal T60 advanced devices.PMS-BUSULFAN 6mg/mL: impurity could be out of specification
The content of an impurity could be out of specification before the expiry date in the affected lots.Medline Disposible Manifolds
Specific items and lots of Medline Manifolds are recalled due to presence of particulate within the fluid path of the Manifolds, with the potential to be introduced…EXENT® Analyser
FSCA initiated due to a software issue affecting the EXENT® Analyser (IE800), whereby QC may not be performed but is indicated as complete under specific conditions…Edwards Lifesciences Swan-Ganz Catheters
There have been a growing number of complaints (outside of Canada) of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on Swan-Ganz catheters.
United StatesXTANT Medical Holdings, Inc recalls nanOss 3D Advanced Bone Graft Substitute nanOss 3D Plus Advanced Bone Graft Substitute…
Products were incorrectly labeled with a 5-year shelf life.Remel Europe Ltd. recalls Oxoid Agglutinating Sera
Affected lots are not performing to IFU criteria showing cross reactions with 2-0 within 60 seconds.Foundation Medicine, Inc. recalls Sequencing Agent SEQ0067
Possible increase in phasing, potentially resulting in false-positive BARD1 splice site indel artifact variantsUvlizer c/o RAIS INTERNATIONAL LLC recalls The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure…
In some foreseeable use conditions, the Products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety…Uvlizer c/o RAIS INTERNATIONAL LLC recalls The product is a handheld ultraviolet-C germicidal wand and contains a combination of…
In some foreseeable use conditions, the products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety…Diversatek Healthcare recalls Diversatek Healthcare Viper¿ 3-Stage Fixed Wire Balloon Dilator and 3 more products
The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.Davol, Inc. recalls Avitene Ultrafoam Microfibrillar Collagen Hemostat
Potential for product to contain foreign matter, confirmed to be inspect fragments.Integra LifeSciences Corp. (NeuroSciences) recalls CUSA Clarity C7000 Console
Software issue that renders the touch screen unresponsive.Foundation Medicine, Inc. recalls Protocol Configuration Tool
Potential for spontaneous closures of Hamilton HxRunControl software during execution of Autolys protocols after deployment of the PCT software for AutoLys Hamilton STAR.Beckman Coulter, Inc. recalls Access Total T4 Calibrator
Beckman Coulter has identified that Access Total T4 Calibrator lots (PN 33805) exhibit a negative bias on DxI 600/800 instruments, with slopes outside product…Micro-X Ltd. recalls Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71
X-Ray generator may malfunction resulting in the X-Ray being inoperable.Windstone Medical Packaging, Inc. recalls Custom Convenience Kits Pre Op Kit and 2 more products
The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump…A little guidance
Get more from your tools
Practical guide 3 min read
Recall classes explained: Class I, II and III
What the FDA's recall classes, Canada's classes and types, and UK and EU alert levels mean, with how often each one comes up.
Practical guide 3 min read
How to check if your car has a recall
Find the recalls for your make and model, confirm with your VIN whether your car is affected, and know what do-not-drive and park-outside warnings mean.
Practical guide 3 min read
What to do if something you own is recalled
Refunds, repairs, replacements and proof of destruction: what to expect, and how to handle recalled food, medicines, batteries and children's products safely.