Safety Recall Directory

Browse and filter the latest official safety alerts globally.

Showing 24 of 72,333 results
Vehicle
NHTSAEQUIPMENT ADAPT...

Blue Bird Body Company - Wheelchair Restraint Retractor May Not Lock

An unsecured wheelchair can move during transit, increasing the risk of injury.

May 20, 2026Blue Bird Body Company
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
ferme la maison rouge - fromage blanc sur lit de fruit
RappelConsovolontaire (san...

ferme la maison rouge - fromage blanc sur lit de fruit

présence de listeria monocytogène

May 20, 2026ferme la maison rouge
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

BW Webster Duo-Decapolar, Product Number D728260RT; REPROCESSED ELECTROPHYSIOLOG...

Incomplete seals on sterile product

May 20, 2026Stryker Sustainability Solutions
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 II

BARD EP XT Decapolar Steerable, Product Number 201007; REPROCESSED ELECTROPHYSIO...

Incomplete seals on sterile product

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

Revolution Apex Plus, X-ray Computed Tomography, Model Number 5590000-25

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
Medical Device
FDA DevicesClass I

1. 3 VALVE MAN KIT, Medline Kit SKU Number: 65101544; 2. 3V MANIFOLD KIT, Med...

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

May 20, 2026Medline Industries, LP
Food & Beverage
FDA FoodClass II

...And Kimchi branded kimchi; packaged in 3 sizes of glass containers (126oz, 63...

Undeclared allergen ingredient (fish)

May 20, 2026Ocinet, Inc.
Medical Device
FDA DevicesClass II

Daig Livewire Steerable, Product Number 401914; REPROCESSED ELECTROPHYSIOLOGY CA...

Incomplete seals on sterile product

May 20, 2026Stryker Sustainability Solutions
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

Brand Name: DONJOY Product Name: ICEMAN W/,UNIV,LOOP,NS,RH Model/Catalog Numbe...

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 401575; REPROCESSED ELECTROPHYSIOLOGY CA...

Incomplete seals on sterile product

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

Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038301; Cardio...

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

May 20, 2026Medline Industries, LP
Vehicle
NHTSAEQUIPMENT

Alliance RV, LLC - Battery Heating Pad May Overheat

The heating pad may overheat in the battery compartment, increasing the risk of a fire.

May 20, 2026Alliance RV, LLC
Medical Device
FDA DevicesClass II

Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom...

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. When the app is running in the background, EGV notifications may queue up and then "replay" sequentially when the user brings the app to the foreground, causing the Glucose Compass to flicker through previous EGVs. In more severe instances, the app may perceive signal loss and deploy signal loss mitigations. This delay in EGV and alert processing creates a risk that users may miss detection of a hypoglycemic or hyperglycemic event, or make treatment decisions based on outdated glucose information.

May 20, 2026Dexcom, Inc.
Medical Device
FDA DevicesClass II

Philips Azurion. System Code Description (Model Number): Azurion 3 M12 (722221, ...

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 the forces applied when the monitor is moved or rotated.

May 20, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical Device
FDA DevicesClass II

On-X Mitral Heart Valve with Conform-X Sewing Ring, Model: ONXMC-25/33

Heart valves were released and distributed before all required testing was complete, so it cannot be confirmed that they meet all release specifications.

May 20, 2026On-X Life Technologies, Inc.
Medical Device
FDA DevicesClass II

Daig Livewire Steerable, Product Number 401603, 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

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
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 II

QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococ...

Product has the potential for false positive results

May 20, 2026Quidel Corporation
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