Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

301–325 of 778

ModerateFDA (Devices)·Z-2166-2026·2026-05-20
Thermedx FluidSmart Urology Tube Set recalled for nonconforming products
Stryker Corporation is recalling the Thermedx FluidSmart Urology Tube Set (Catalog No. LL0006) due to nonconforming products that were inadvertently distributed. The affected tube sets were distributed nationwide in Georgia.
Product
Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The FluidSmart Tube Sets are intended to be used with the FluidSmart Fluid Management System, which is intended for irrigation and fluid warming in laparoscopic procedures, and distention, fluid warmi
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2153-2026·2026-05-20
Revolution CT ES X-ray Computed Tomography System Security Vulnerability Recall
GE Medical Systems is recalling Revolution CT ES and related CT systems due to a potential security vulnerability in the AW Server deployed via Edison Health Link based CT Smart Subscription. The vulnerability may affect system security.
Product
Revolution CT ES, X-ray Computed Tomography, Model Number 5590000-15
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2170-2026·2026-05-20
Philips Azurion X-Ray System Cable Hose Carriers May Loosen or Break
Bolts and plastic parts of cable hose carriers on Philips Azurion X-ray systems may loosen or break during monitor movement or rotation, potentially causing the cable hose to become unsecured.
Product
Philips Azurion. System Code Description (Model Number): Azurion 3 M12 (722221, 722229), Azurion 3 M15 (722222, 722230), Azurion 5 (722281), Azurion 5 M12 (722227, 722231), Azurion 5 M20 (722228, 722232, 722281), Azurion 7 (722282), Azurion 7 B12 (722225, 722235), Azurion 7 B20 (
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2173-2026·2026-05-20
Codman CerebroFlo EVD Catheter recalled for out-of-specification endotoxin
Integra LifeSciences is recalling Codman CerebroFlo EVD Catheters (Lot 45322) because endotoxin levels did not meet acceptance criteria. The product was distributed nationwide.
Product
Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.550.501. The CerebroFlo EVD Catheter is a 3.3 mm diameter (10 Fr.), 35 cm long polyurethane catheter for diverting cerebrospinal fluid (CSF) from the ventricles of the brain through a series
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2162-2026·2026-05-20
Diowave Laser System Software Update Required for Power Output Issue
Diowave 250W Laser Systems require a software update because some units operate at up to 70W maximum average power output, exceeding the FDA-cleared limit of 60W.
Product
Diowave Laser System, REF: Diowave 250W
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2150-2026·2026-05-20
Revolution CT X-ray Computed Tomography System Security Vulnerability Recall
GE HealthCare is recalling Revolution CT x-ray computed tomography systems due to a potential security vulnerability in the AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription. The vulnerability affects certain Revolution Apex, Revolution Ascend, and Revolution CT systems worldwide.
Product
Revolution CT, x-ray computed tomography, Model Numbers 5590000 and 5590000-6
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2151-2026·2026-05-20
Revolution Apex Elite X-ray CT System Security Vulnerability Recall
GE HealthCare is recalling certain Revolution Apex Elite X-ray computed tomography systems due to a potential security vulnerability in the AW Server deployed via Edison Health Link. The vulnerability may affect data security in CT Smart Subscription systems.
Product
Revolution Apex Elite, X-ray Computed Tomography, Model Number 5590000-23
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0512-2026·2026-05-15
Sliced Deli Turkey Recalled Nationwide Over Listeria Risk
Northfield Foods is recalling 187,000 lbs of sliced deli turkey after Listeria was found during routine testing.
Product
Northfield Select — Oven-Roasted Sliced Turkey Breast
Category
Food
Distribution
Distributed nationwide
SevereCPSC·26485·2026-05-14
Agio Menlo Woven Patio Swings Recalled Due to Fall Hazard Risk
World Bright International Limited recalls Agio Menlo Woven Patio Swings (Model 1934256) sold at Costco because the swing seat can detach during use, risking serious injury or death. Eight injuries have been reported.
Product
Agio Menlo Woven Patio Swings
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26490·2026-05-14
Guidecraft Kitchen Helper Towers Recalled Due to Fall Hazard Risk
Guidecraft Kitchen Helper Towers are being recalled because the internal platform can loosen, become unstable, or detach, creating a fall hazard for young children. The company has received 11 reports of falls, including three injuries.
Product
Guidecraft Kitchen Helper Towers
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26482·2026-05-14
Can-Am Outlander Pro and Max Pro All-Terrain Vehicles Speed Limiter Malfunction
BRP US Inc. recalls about 2,820 Can-Am Outlander Pro and Max Pro ATVs with defective Speed Limiter Mode that can cause unexpected speed and acceleration, posing a risk of serious injury or death from crashes.
Product
Can-Am Outlander Pro and Max Pro All-Terrain Vehicles
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·26493·2026-05-14
Cosyland Children's Tower Stools Recalled for Entrapment and Fall Hazards
Cosyland Children's Tower Stools can collapse, tip over, or trap a child's torso through front and back openings, posing risks of serious injury and death. The firm is aware of 25 reports of stability issues and falls, with eight injuries including a fractured arm.
Product
Cosyland Children's Tower Stools
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26494·2026-05-14
Electric Start Pressure Washers Recalled for Carbon Monoxide Hazard
Generac and DR Power electric start pressure washers are recalled because the electronic start/stop button can malfunction and self-start the unit, creating a risk of serious injury or death from carbon monoxide poisoning in confined spaces. No injuries have been reported.
Product
Electric Start Pressure Washers
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26479·2026-05-14
Minka Bardon Series Pendant Light Fixtures Recalled Due to Impact Hazard
Minka Lighting Group is recalling about 170 Bardon Series Pendant Light Fixtures because the frame can detach from the downrod during installation, posing a risk of serious injury or death. One detachment has been reported with no injuries yet.
Product
Minka Bardon Series Pendant Light Fixtures
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26481·2026-05-14
Tiyol Pull String Teething Toys Recalled for Choking Hazard Risk
Tiyol Pull String Teething Toys sold on Amazon are recalled due to oversized silicone strings that can lodge in the throat, posing a choking hazard. CPSC is aware of 11 choking incidents.
Product
Tiyol Pull String Teething Toys
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·26483·2026-05-14
Misco Sports Badminton Toy Sets Recalled Due to Battery Ingestion Risk
Missry Associates is recalling Misco Sports Badminton Toy Sets because the shuttlecocks contain button cell batteries that children can easily access and swallow, potentially causing serious internal injuries or death.
Product
Misco Sports Badminton Toy Sets Red/Blue MT2383
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26480·2026-05-14
Superbobi Pool Drain Covers Recalled for Entrapment and Drowning Risk
Superbobi 7 3/8-inch pool drain covers violate federal safety standards and pose entrapment and drowning hazards. Pool owners should stop using affected covers immediately.
Product
Superbobi 7 3/8 Inch Pool Drain Covers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26487·2026-05-14
Petzl Climbing and Adventure-Park Harnesses Recalled for Fall-Hazard Risk
Petzl America is recalling about 1,270 SIMBA and SWAN EASYFIT harnesses because missing rivets in the buckles can cause them to open, creating a risk of serious injury or death from falls.
Product
Petzl SIMBA CLIMBING and SIMBA PARK Children's Harnesses, SWAN EASYFIT STEEL and SWAN EASYFIT STAINLESS Harnesses
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26489·2026-05-14
Electric Water Kettles Recalled Due to Burn Hazard from Loosening Handle
ZWILLING J.A. Henckels has recalled approximately 113,440 ENFINIGY electric kettles in the U.S. because the handle can loosen and separate, causing hot water to spill and posing a burn injury risk.
Product
Electric Kettles (ENFINIGY 1.5 l and ENFINIGY Pro 1.5 l)
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26488·2026-05-14
Petzl America Recalls Three Climbing Harness Models for Fall Hazard
Petzl America is recalling about 29,300 climbing harnesses because the D-ring attachment point can release, creating a risk of serious injury or death from a fall.
Product
Petzl ASTRO BOD FAST, ASTRO SIT FAST and CANYON GUIDE harnesses
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26484·2026-05-14
LiCB CR2032 Lithium Coin Batteries Recalled for Child-Resistant Packaging Violation
Guangzhou Lichengbei Battery Technology Co., Ltd. (LiCB) has recalled about 94,000 CR2032 3V lithium coin batteries sold on Amazon because they lack required child-resistant packaging and warning labels. Ingestion can cause serious internal injuries, chemical burns, and death.
Product
LiCB CR2032 3V Lithium Coin Batteries
Category
Consumer Product
Distribution
Distributed nationwide
ModerateCPSC·26486·2026-05-14
Amazon Basics 55 Lbs. Adjustable Dumbbells Recalled for Impact Hazard
Amazon is recalling Amazon Basics 55 Lbs. Adjustable Dumbbells because weight plates can fail to engage completely and dislodge during use, posing an impact hazard. No injuries have been reported.
Product
Amazon Basics 55 Lbs. Adjustable Dumbbells
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1934-2026·2026-05-13
Cook Centimeter Sizing Catheter recall due to marker band cracking
Cook Incorporated is recalling Centimeter Sizing Catheters because marker bands may crack or break, potentially causing device fragmentation, vessel injury, or life-threatening harm.
Product
Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20 GPN G11916 Catheters for use in angiographic procedures are available in a variety of French sizes, endhole sizes, lengths, materials and designs (e.g., polyethylene or nylon, non-braided or braided with 1:1 torque)
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1935-2026·2026-05-13
Aurous Centimeter Sizing Catheter Recalled for Marker Band Cracking Risk
Cook Incorporated is recalling Aurous Centimeter Sizing Catheters due to risk of marker band cracking or breakage during angiographic procedures. Potential complications include device fragmentation, vessel injury, and in worst-case scenarios, life-threatening harm or death.
Product
Aurous Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20-01 GPN G47308 Sizing catheters are single-use, sterile catheters with gold marker bands. These catheters are for use in angiographic procedures and available in a variety of lengths (70 and 100 cm) and tip co
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1977-2026·2026-05-13
Halyard PERC TRAY Kit Syringe Adaptor Connection Risk Recall
The Halyard PERC TRAY kit (models SLPC34-01 and SLPC34-02) is being recalled due to risk that a Medline syringe rotating adaptor may unwind during use, causing a loose or full disconnection between the syringe and manifold.
Product
Halyard PERC TRAY kit. Model Numbers: SLPC34-01, SLPC34-02.
Category
Medical Device
Distribution
7 states

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