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Recalls from the FDA, USDA FSIS, CPSC and NHTSA, newest first.
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26 recalls

Medtronic Abre Venous Self-Expanding Stent System

The Abre Venous Self-Expanding Stent System may have a Nitinol anomaly causing reduced stent diameter and radial force, potentially leading to migration.

Moderate risk, FDA, Device defect

Instrumentation Laboratory Coagulation Testing Reagents

The product has potential for microbial contamination.

Moderate risk, FDA, Contamination

ICU Medical Pulsator Arterial Blood Sampling Kit and Portex Spinal Tray

Pulsator Arterial Blood Sampling Kit and Portex Spinal Tray may have cracked syringe collars, leading to delayed or repeated blood draw or fluid leakage.

Moderate risk, FDA, Device defect

Intuitive Surgical da Vinci SP Access Port Kit

The da Vinci SP Access Port Kit may develop cracks, potentially causing a sterility breach.

Moderate risk, FDA, Sterility problem

20 recalls

Encon Safety Products Aquarion Preserved Cartridges

The Aquarion Preserved Cartridges have cGMP deviations.

Moderate risk, FDA, Manufacturing problem

Advanced Pharmaceutical Technology TESTO-100 CIII Testosterone Pellets

Testo-100 Ciii (testosterone 100 mg) pellets may lack assurance of sterility due to potential microbial contamination.

Moderate risk, FDA, Sterility problem

C-RAD Catalyst+ Patient Positioning Devices

The Catalyst and Catalyst+ patient positioning device may show a patient as correctly positioned even when the isocenter is outside tolerance.

Moderate risk, FDA, Device defect

Sun Pharmaceutical Clindamycin Phosphate Topical Solution

Failed Impurities/Degradation: Out of Specification results for Total Impurities and for Assay.

Low risk, FDA, Drug impurity

Philips Azurion Systems

Philips Azurion Systems R3.0 have software issues that may cause loss of X-ray and other problems.

Moderate risk, FDA, Software defect

PALACOS Bone Cement Mixing and Application Systems

Palacos bone cement may have ampoules that do not break, so the product cannot be used on the patient.

Moderate risk, FDA, Device defect

Healthy Truth Moringa Powder

Healthy Truth brand Moringa Powder may be contaminated with Salmonella Richmond.

High risk, FDA, Salmonella

Philips Azurion Systems

Philips Azurion Systems have software issues that may cause system restarts and positional errors.

Moderate risk, FDA, Software defect

Sanders Candy Factory Frosted Almond

Frosted Almond contains elevated levels of aflatoxin.

Moderate risk, FDA, Chemical contamination

Ukrop's Pound Cakes with Buttercream Icing

Ukrop's pound cakes with buttercream icing may contain undeclared soy.

Moderate risk, FDA, Undeclared soy

AZ Gems Jumbo Raw Shrimp

Jumbo raw shrimp have elevated levels of chloramphenicol.

Moderate risk, FDA, Chemical contamination

So Delicious Dairy Free Salted Caramel Cluster Cashewmilk Non-Dairy Frozen Dessert

The frozen dessert contains foreign material.

Moderate risk, FDA, Foreign object

Diagnostica Stago Asserachrom HPIA Kits

Asserachrom HPIA can produce negative results due to a defect affecting every well in the impacted strip.

Moderate risk, FDA, Device defect

Fran's PureBar Almondmilk Chocolate

The chocolate contains undeclared hazelnut.

High risk, FDA, Undeclared tree nut

Medline Medical Procedure Convenience Kits

Medline medical procedure convenience kits can leak and emit vaporized saline that resembles smoke during use.

Moderate risk, FDA, Device defect

Troemner Family Farm Pfeffernusse Cookies

Troemner Family Farm Pfeffernusse Cookies contain undeclared soy, wheat, and milk.

High risk, FDA, Undeclared milk

One Roof Atwater's Holiday Cookie Tin

The Atwater's Holiday Cookie Tin contains undeclared tree nut allergens.

High risk, FDA, Undeclared tree nut

Alvogen Levothyroxine Sodium Tablets Thy-Tabs

Levothyroxine Sodium Tablets, USP, Thyro-Tabs may contain 88 mcg tablets instead of 150 mcg tablets.

Moderate risk, FDA, Labeling error

Gold Star Distribution Advil, Aleve, Tylenol and More Over-the-Counter Medicines

Gold Star Distribution medicines have CGMP deviations.

Moderate risk, FDA, Manufacturing problem

WFM Purchasing Brussel Sprouts & Kale Slaw

Brussel Sprouts & Kale Slaw contains undeclared fish and egg allergen.

High risk, FDA, Undeclared egg

7 recalls

East Trailers Beast and Beast II Trailers

Beast and Beast II trailers have an improper weld that may fail, causing the rear impact guard to detach.

NHTSA, Vehicle structure defect

Lippert 3000 Series Hidden Hinge Ramp Doors

The 3000 Series Hidden Hinge Ramp Door may break away from the frame while loading or unloading vehicles, increasing injury risk.

NHTSA, Vehicle equipment defect

Philips Allura Xper FD10, FD20 and Biplane Systems

Philips Allura Xper systems may have a missing drip tray, allowing coolant to contact electrical components and cause short-circuits.

Moderate risk, FDA, Device defect

Canon Medical Vantage Galan 3T and Vantage Titan 3T MRI Systems

If a quench occurs, helium gas may not escape, and pressure in the helium vessel may rise.

Moderate risk, FDA, Device defect

Elekta MOSAIQ Oncology Information System with Particle Therapy License

The Mosaiq Oncology Information System with Particle Therapy License may deliver partial treatment twice, causing overtreatment.

Moderate risk, FDA, Foreign object

Taro Pharmaceuticals Fluocinolone Acetonide Topical Solution

Fluocinolone Acetonide Solution Topical Solution failed impurity specifications due to an out-of-specification result for known impurity D.

Low risk, FDA, Drug impurity

Repligen Maverick Measurement Module Spectrometer

The Maverick Measurement Module Spectrometer can have elevated laser output or unintended laser firing due to cable issues.

Moderate risk, FDA, Device defect

7 recalls

Outside The Breadbox Bread Crumbs

Undeclared allergens: egg and milk.

High risk, FDA, Undeclared milk

Karison Besan Laddoo, Punjabi Pinni, Alsi Pinni and Panjiri

Karison brand snacks contain undeclared milk, posing a risk of serious allergic reaction.

Moderate risk, FDA, Undeclared milk

Spring & Mulberry Date-Sweetened Chocolate

Spring & Mulberry Date-Sweetened Chocolate bars may be contaminated with Salmonella, which can cause serious infections.

High risk, FDA, Salmonella

Terex: TL-Series, LT-Series, LTM40, and 3 more (2025)

The hydraulic equipment may overheat, and touching it can increase the risk of burn injuries.

NHTSA, Vehicle equipment defect

Fresenius Kabi Ivenix Infusion System LVP Software

The Ivenix Infusion System LVP Software has instructions for LVP duration programming that are emphasized in the IFU.

Moderate risk, FDA, Software defect

HANGZHOU BEVER MEDICAL DEVICES BD Ready-to-Use Hydrophilic Catheter

The BD Ready-to-Use Hydrophilic Catheter has a labeling error with an incorrect expiration date.

Moderate risk, FDA, Labeling error

Medline Kits With B. Braun IV Administration Sets

Medline kits containing B. Braun IV administration sets may have check valves that stick.

Moderate risk, FDA, Device defect

14 recalls

Diva Fam Sea Moss Gel Superfood

Sea Moss Gel Superfood may be contaminated with C. botulinum (botulism), which can cause botulism, a serious illness affecting the nervous system.

Moderate risk, FDA, Botulism

Herbs Forever Ayurvedic Herbal Supplements

HerbsForever Hingwastik Churna and Gastro Care dietary supplements may contain undeclared wheat, posing a risk of serious allergic reactions.

High risk, FDA, Undeclared wheat

Modern Warrior Life Ready Dietary Supplement

Modern Warrior Ready contains undeclared ingredients that can cause life-threatening events and cardiovascular problems.

High risk, FDA, Hidden drug ingredient

Land Rover 2026 Range Rover Sport Vehicles

The 2026 Range Rover Sport has incorrect weight information on its certification label, which could lead to overloading and increase crash risk.

NHTSA, Vehicle equipment defect

Goodyear Cooper Discoverer SRX Tires

Cooper Discoverer SRX tires have an incorrect Tire Identification Number, which can prevent owners from properly registering them.

NHTSA, Tire defect

Eureka Cinnamon

Cinnamon in a clear plastic container has elevated levels of lead.

Moderate risk, FDA, Chemical contamination

Tops Strawberry and Mixed Fruit Jam

Mangalm is recalling its Tops Strawberry Jam and Tops Mixed Fruit Jam because of Unapproved color (carmoisine).

Moderate risk, FDA, Undeclared color or additive

Medicrea IB3D Universal Implant Inserter and PL Instruments Set

Medicrea IB3D Universal Implant Inserter and PL Instruments Set may have a handle that untreads, causing inability to rotate implant.

Moderate risk, FDA, Device defect

Medtronic Vanta Clinician Programmer Application

The A71200 Vanta Clinician Programmer Application may not function as intended, potentially causing a prolonged or postponed surgical procedure.

Moderate risk, FDA, Device defect

Mobius Imaging AIRO Computed Tomography X-Ray System Pendants

AIRO pendant replacement kits and upgrade do not possess the "Safe Hand Position Warning" label.

Moderate risk, FDA, Labeling error

GE Medical Systems Israel Emission Computed Tomography Systems

Certain Nuclear Medicine systems could have been transported or relocated without adequate detector support.

Moderate risk, FDA, Device defect

Boston Scientific Coyote Over-the-Wire PTA Balloon Dilation Catheters

The Coyote balloon catheter may not inflate or deflate properly during use.

Moderate risk, FDA, Device defect