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

551–575 of 29593

HighFDA (Devices)·Z-2164-2026·2026-05-20
[pending] Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM watchOS App
Pending LLM rewrite. Source: FDA_DEVICE Z-2164-2026.
Product
Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM watchOS App Model/Catalog Number: SW13355 Software Version: Versions 2.9.0 through 2.11.2 Product Description: Dexcom G7 CGM watchOS App - The watchOS app is installed along with the iOS ph
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2180-2026·2026-05-20
Reprocessed Electrophysiology Catheter Recalled for Incomplete Seals
Stryker Sustainability Solutions is recalling BARD Dynamic XT Steerable reprocessed electrophysiology catheters due to incomplete seals on the sterile product, which could compromise sterility.
Product
BARD Dynamic XT Steerable, Product Number 201104; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2185-2026·2026-05-20
Reprocessed Electrophysiology Catheter Recall Due to Incomplete Seals
Stryker Sustainability Solutions is recalling 816 units of CS Uni-Directional w Auto ID reprocessed electrophysiology catheters due to incomplete seals on the sterile product packaging.
Product
CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2165-2026·2026-05-20
Dexcom ONE+ iOS CGM App Software Defect Delayed Glucose Alerts
Dexcom, Inc. is recalling Dexcom ONE+ iOS CGM App versions 1.5.0 and 1.6.0 due to a software defect that can delay glucose alerts and notifications, risking delayed detection of low or high blood sugar events.
Product
Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name: Dexcom ONE+ iOS CGM App Model/Catalog Number: SW14244 Software Version: versions 1.5.0 and 1.6.0 Product Description: Dexcom ONE+ iOS CGM App Component: Dexcom ONE+ Continuous Glucose Monitoring Syste
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2197-2026·2026-05-20
Daig Livewire Steerable Reprocessed Electrophysiology Catheter Recall
Stryker Sustainability Solutions is recalling 458 units of Daig Livewire Steerable reprocessed electrophysiology catheters due to incomplete seals on the sterile product packaging.
Product
Daig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2189-2026·2026-05-20
Daig Livewire Steerable Electrophysiology Catheters Recalled for Incomplete Seals
Stryker Sustainability Solutions is recalling Daig Livewire Steerable electrophysiology catheters with incomplete seals on sterile packaging. The defect may allow contamination of the sterile product.
Product
Daig Livewire Steerable, Product Number 401603, REPROCESSED ELECTROPHYSIOLOGY CATHETER
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2184-2026·2026-05-20
[pending] CS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Pending LLM rewrite. Source: FDA_DEVICE Z-2184-2026.
Product
CS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2193-2026·2026-05-20
Daig Livewire Steerable Electrophysiology Catheter Sterile Seal Defect Recall
Stryker Sustainability Solutions is recalling three lots of Daig Livewire Steerable reprocessed electrophysiology catheters due to incomplete seals on the sterile packaging. The defect affects units distributed in the US, Israel, and Canada.
Product
Daig Livewire Steerable, Product Number 401908; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2183-2026·2026-05-20
Reprocessed Electrophysiology Catheter Recalled for Incomplete Sterile Seals
Stryker Sustainability Solutions is recalling 154 units of BW Webster Duo-Decapolar reprocessed electrophysiology catheters due to incomplete seals on the sterile product packaging, which may compromise sterility.
Product
BW Webster Duo-Decapolar, Product Number D728260RT; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2198-2026·2026-05-20
Daig Livewire Steerable BDB Electrophysiology Catheter Recall
Stryker Sustainability Solutions is recalling Daig Livewire Steerable BDB reprocessed electrophysiology catheters due to incomplete seals on the sterile product.
Product
Daig Livewire Steerable BDB, Product Number 401918, REPROCESSED ELECTROPHYSIOLOGY CATHETER
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2175-2026·2026-05-20
BARD Dynamic Tip Steerable Reprocessed Electrophysiology Catheter Recall
Stryker Sustainability Solutions is recalling BARD Dynamic Tip Steerable reprocessed electrophysiology catheters (Product Number 200131) due to incomplete seals on sterile product packaging. The recall affects 61 units distributed nationwide in the US and in Israel and Canada.
Product
BARD Dynamic Tip Steerable, Product Number 200131; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0768-2026·2026-05-20
[pending] Dakota Honey Company Spreadable Spun Honey, Original. Stir before use. Produced in Winner, SD. Pa
Pending LLM rewrite. Source: FDA_FOOD H-0768-2026.
Product
Dakota Honey Company Spreadable Spun Honey, Original. Stir before use. Produced in Winner, SD. Packaged in the following sized plastic jars: 1. Net Wt 4 oz (113g) UPC 8 60010-57969 5. 2. Net Wt 12 oz (340g) UPC 8 60010-57961 9.
Category
Food
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·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·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·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·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
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·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·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·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
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
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·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

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