Medicine, medical device and cosmetics recalls
Recalls of medicines, medical devices, supplements, cosmetics and personal care products.
2,312 recalls, newest first · Checked 4 minutes ago
CanadaNeurological Sponges
During an internal review, Medicom has identified the potential for unexpected variability of endotoxin levels on the products.HarmonyAIR A-Series Surgical Lighting System AND ALYON Surgical Lighting System
Steris identified through customer complaints that on Harmonyair A-Series Lighting System and Alyon Surgical Lighting System the plus/minus (+/-) buttons that control…Honibe Honey Gummies - Melatonin: Daily recommended intake may cause the active ingredient to exceed the allowable limit.
The maximum daily intake may cause the active ingredient to exceed the allowable limit.ERYTHROMYCIN OPHTHALMIC OINTMENT USP: The sterility of the product could be compromised.
The sterility of the product could be compromised in the affected lot.Personnelle Supravite Energizing Formula: The breakage of vials can generate glass fragments
The breakage of vials can generate glass fragments.Exoplan
During internal testing of libraries an error was identified within specific Straumann surgical protocol libraries used with Exoplan version 3.1.
CannaPiece Corp. recalls JAYs - Pink Pennifer 0.4g all-in-one vape due to labelling issue
The label for the affected product has incorrect cannabinoid values.
United StatesJolife AB recalls LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code…
Due to a subset of chest compression systems/devices where the service performed on the systems were not appropriately documented (The documents for the service…Integra LifeSciences Corp. (NeuroSciences) recalls Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID…
Out-of-specification endotoxin result that did not meet the acceptance criteria.Edwards Lifesciences, LLC recalls Edwards EVOQUE tricuspid delivery system REF:9850TDS Sterile EO
Labeling update to provide warning if functionality of the valve replacement delivery system is compromised.Philips Medical Systems Nederland B.V. recalls Philips Azurion. System Code Description
Potential for the bolts and plastic parts of the Cable Hose Carriers that hold the cable hose to the monitor ceiling suspension may loosen and/or break over time due to…Technological Medical Advancements LLC recalls Diowave Laser System
Software update is needed for laser systems, for topical infrared heating to provide temporary relief of minor muscle and joint pain, spasms, stiffness associated with…Aniara Diagnostica LLC recalls ZYMUTEST HIA IgG
Kits from lot FD1265 had been packaged on 17 October 2024 and put on the market with an outdated flyer (8 October 2024), containing incorrect values for the positive…Dexcom, Inc. recalls Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM… and 2 more products
A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs) and trend arrows.Quidel Corporation recalls QuickVue Dipstick Strep A Test
Product has the potential for false positive resultsStryker Corporation recalls Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The…
Due to nonconforming products being inadvertently distributed.Arrow International, LLC recalls Arrow Edge Hemodialysis Catheterization Product and 3 more products
16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets.On-X Life Technologies, Inc. recalls On-X Mitral Heart Valve with Conform-X Sewing Ring
Heart valves were released and distributed before all required testing was complete, so it cannot be confirmed that they meet all release specifications.Windstone Medical Packaging, Inc. recalls Custom Convenience Kit containing recalled Medline Namic Angiographic Control Syringes…
Affected kits contain Medline Namic RA Syringes, which are recalled by their manufacturer due to risk of syringe rotating adapter unwinding during use, which may result…Medtronic Neuromodulation recalls Medtronic SynchroMed Flex Infusion Mode
Software issue: When programming the SynchroMed Pump with the A810 CP App in Flex Infusion Mode, the infusion steps should automatically be arranged in consecutive…Omnicell, Inc. recalls Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028
Potential for mislabeled syringe produced by the i.v.STATION device.Hologic, Inc recalls SELENIA DIMENSIONS MAMMOGRAPHY SYSTEMS. Model Numbers: SDA-SYS-3000-2D-HTC and 1 more products
Complaints have been received of systems developing loose, missing, or broken internal bolts over time.Djo, LLC recalls Brand Name: DONJOY Product Name: ICEMAN CLASSIC CUBE Model/Catalog Number: 11-0494… and 3 more products
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.A little guidance
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