Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 72,371 results
Medical Device
FDA DevicesClass II

Revolution Ascend, computed tomography, Model Numbers 6969000-100 and 6969000-30...

GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain Revolution Apex, Revolution Ascend, and Revolution CT systems.

May 20, 2026GE Medical Systems, LLC
Food & Beverage
FDA FoodClass II

Dakota Honey Company Spreadable Spun Honey, Jalapeno. Stir before use. Produc...

Foreign object (stainless steel dust/flakes or shreds of plastic)

May 20, 2026Dakota Honey Company
Medical Device
FDA DevicesClass I

Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258...

Potential for mislabeled syringe produced by the i.v.STATION device.

May 20, 2026Omnicell, Inc.
Food & Beverage
FDA FoodClass II

Dakota Honey Company Spreadable Spun Honey, Original. Stir before use. Produce...

Foreign object (stainless steel dust/flakes or shreds of plastic)

May 20, 2026Dakota Honey Company
Medical Device
FDA DevicesClass II

Diowave Laser System, REF: Diowave 250W

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 minor arthritis, and to temporarily increase local blood circulation, operating at a maximum average power output of 70W, which is beyond the FDA cleared 60W.

May 20, 2026Technological Medical Advancements LLC
Medical Device
FDA DevicesClass II

Brand Name: DONJOY Product Name: ICEMAN CLASSIC CUBE Model/Catalog Number: 11-...

Due to broken connector which may result in a temporary interruption of prescribed cold therapy.

May 20, 2026DJO, LLC
Medical Device
FDA DevicesClass II

Daig Livewire Steerable, Product Number 401923; REPROCESSED ELECTROPHYSIOLOGY CA...

Incomplete seals on sterile product

May 20, 2026Stryker Sustainability Solutions
Medical Device
FDA DevicesClass II

Edwards EVOQUE tricuspid delivery system REF:9850TDS Sterile EO

Labeling update to provide warning if functionality of the valve replacement delivery system is compromised.

May 20, 2026Edwards Lifesciences, LLC
Medical Device
FDA DevicesClass I

Medline medical convenience kits, containing Namic Manifold, Labeled as: 1. M...

Medline has identified the presence of particulate within the fluid path of the Manifolds.

May 20, 2026Medline Industries, LP
Medical Device
FDA DevicesClass I

NextStep Antegrade Chronic Hemodialysis Catheter, REF: AC-15192-SFX, AC-15232-SF...

16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and may result in withdrawal resistance, prolonged procedure time, pain, bleeding, hematoma, tissue injury, vessel wall injury.

May 20, 2026ARROW INTERNATIONAL, LLC
Medical Device
FDA DevicesClass I

Arrow Edge Hemodialysis Catheterization Product, REF: CS-15242-I, CS-15282-I, CS...

16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and may result in withdrawal resistance, prolonged procedure time, pain, bleeding, hematoma, tissue injury, vessel wall injury.

May 20, 2026ARROW INTERNATIONAL, LLC
Medical Device
FDA DevicesClass II

Daig Livewire Steerable, Product Number 401603, REPROCESSED ELECTROPHYSIOLOGY CA...

Incomplete seals on sterile product

May 20, 2026Stryker Sustainability Solutions
Food & Beverage
FDA FoodClass II

Dakota Honey Company Spreadable Spun Honey, Cinnamon-Infused. Stir before use. ...

Foreign object (stainless steel dust/flakes or shreds of plastic)

May 20, 2026Dakota Honey Company
Medical Device
FDA DevicesClass II

LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UD...

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 performed to justify the passing results were not include in the service records).

May 20, 2026Jolife AB
Medical Device
FDA DevicesClass II

Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 ...

Due to nonconforming products being inadvertently distributed.

May 20, 2026Stryker Corporation
Medical Device
FDA DevicesClass I

Medline medical convenience kits, containing Namic Manifold, Labeled as: 1. A...

Medline has identified the presence of particulate within the fluid path of the Manifolds.

May 20, 2026Medline Industries, LP
Medical Device
FDA DevicesClass I

Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038200; Cardio...

Medline has identified the presence of particulate within the fluid path of the Manifolds.

May 20, 2026Medline Industries, LP
Medical Device
FDA DevicesClass I

Arrow-Clark VectorFlow Antegrade Chronic Hemodialysis Catheter: REF: ACS-15192-V...

16F dual-valved splittable sheath introducer, the subject of a supplier recall, was included in impacted hemodialysis kits & sets. Sheath introducer may not split as intended, and may result in withdrawal resistance, prolonged procedure time, pain, bleeding, hematoma, tissue injury, vessel wall injury.

May 20, 2026ARROW INTERNATIONAL, LLC
Food & Beverage
Germany BVLGeneral Alert

Mais Waffeln Salted Caramel, 50 Gramm

Rückstände und Kontaminanten

May 19, 2026Inverkehrbringer/ Hergestellt für: Dirk Rossmann GmbH Isernhägener Straße 16 DE-30938 Burgwedel
Safety Alert
Health CanadaClass 2

Blackstone brand Parmesan Ranch Seasoning recalled due to Salmonella

Salmonella

May 19, 2026CFIA
Vehicle
NHTSAFORWARD COLLISI...

Hyundai Motor America - Forward Collision Avoidance System May Activate Brakes U...

Unexpected braking increases the risk of a crash.

May 19, 2026Hyundai Motor America
Safety Alert
Health CanadaGeneral Alert

1-K Kerosene Heater Fluid Portable Fuel Containers recalled due to fire hazard

Fire hazard

May 19, 2026Consumer product safety
Safety Alert
Health CanadaGeneral Alert

Transport Canada Recall - 2026225 - FIAT CHRYSLER AUTOMOBILES

Powertrain

May 19, 2026TC
Safety Alert
Health CanadaType II

Honibe Honey Gummies - Melatonin: Daily recommended intake may cause the active ...

Product quality

May 19, 2026Drugs and health products
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