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Search or scan any product against every CPSC, FDA, USDA, and NHTSA recall on record — or read the last 90 days below.
- 2026-07-16CPSCWuxi Leclaire Home Products Co., Ltd., of ChinaWade Logan Annyka dressers recalled for tip-over risk
Wade Logan Annyka 9-Drawer Fabric Dressers can tip over and trap children if not anchored to the wall. These dressers do not meet federal safety standards for furniture stability. About 180 units were sold online at Wayfair.com between September 2023 and May 2026.
- 2026-07-16CPSCCurrey & Company, of Atlanta, GeorgiaCurrey & Company Nottaway chandeliers recalled for electrocution risk
Currey & Company's Nottaway chandeliers lack proper electrical grounding, which can cause electrocution. The affected two-tier and three-tier models were sold in gold, bronze, and champagne finishes between November 2025 and May 2026. Only chandeliers with no visible screw on the outside of the top distributor cap are affected.
- 2026-07-16CPSCTOMY International, Inc., of Oak Brook, IllinoisTOMY Boon PIVOT step stool recalled for tip-over risk
The Boon PIVOT toddler tower kitchen step stool can tip over or shift during use, creating a risk of serious injury. TOMY has received 11 reports of the stools becoming unstable or leaning, though no injuries have been reported yet.
- 2026-07-16CPSCShenzhen Gudebo Technology Co. Ltd., of ChinaLiizousuda paint thinner recalled for child poisoning risk
Liizousuda paint thinner bottles sold on Amazon have regular caps that children can open easily. The product contains petroleum distillates that can cause serious injury or death if swallowed, and can damage the lungs if inhaled. Federal law requires this type of product to have child-resistant packaging.
- 2026-07-16CPSCPanasonic Manufacturing (Xiamen) Co., Ltd, of Xiamen, Fujian, ChinaPanasonic toaster oven recalled for shock and fire risk
The power cord on Panasonic Model NB-G200 electric toaster ovens may not be adequately insulated due to a protective fiberglass sleeve that doesn't cover it properly. This can create a risk of electric shock or fire. Four consumers have reported tripped circuit breakers or outlets, but no fires or injuries have occurred so far.
- 2026-07-16CPSCShenzhen Dami Trading Co., Ltd., dba Delightmi, of ChinaOitnlaughter finger lights recalled for battery ingestion risk
These LED finger lights contain button cell batteries that children can easily access and swallow. Swallowing these batteries can cause serious internal injuries, including chemical burns, and can be fatal.
- 2026-07-15FDA-PRKhong GuanKhong Guan rice balls recalled for undeclared peanuts
Khong Guan Corporation is recalling Glutinous Rice Balls with Black Sesame Filling and Black & White Glutinous Rice Balls with Black Sesame Filling because they may contain peanuts that are not listed on the packaging. People with peanut allergies could have a serious allergic reaction. No illnesses have been reported so far.
- 2026-07-14NHTSA-EquipmentFord Motor CompanyFord Motor Company - Trailer Brakes and Lighting May Be Lost/FMVSS 108
A loss of trailer brakes or lights can reduce the driver’s ability to control the trailer and decrease the trailers visibility to other road users, increasing the risk of a crash.
- 2026-07-13FDA-PRKhong Guan CorporationKhong Guan rice balls recalled for undeclared peanuts
Khong Guan Corporation is recalling Glutinous Rice Balls with Black Sesame Filling (14.1 oz bags) because they may contain undeclared peanuts. People with peanut allergies or sensitivities could have serious or life-threatening reactions. No illnesses have been reported.
- 2026-07-10NHTSA-EquipmentTenneco AutomotiveTenneco Automotive - Loss of Steering
A loss of steering increases the risk of a crash.
- 2026-07-10NHTSA-EquipmentZoox, Inc.Zoox, Inc. - ADS Software May Fail to Detect and Respond to Heavy Smoke
Failing to respond to low visibility conditions can increase the risk of a crash or impede first responders.
- 2026-07-09CPSCGreenworks North America, LLC, dba Greenworks Tools, of Mooresville, North CarolinaGreenworks Tools Recalls 24V and 48V Kobalt Yard Power Tools with USB-C Batteries Due to Risk of Serious Injury from Fire Hazard
Charging the lithium-ion batteries through the USB-C port, while the batteries are inserted in the yard power tools can cause the batteries to short-circuit, posing a risk of serious injury from fire hazard.
- 2026-07-09CPSCiDecoz Inc. dba Flaunt, of Brooklyn, New YorkFlaunt MagSafe Battery Charger recalled for fire risk
The lithium-ion battery in Flaunt MagSafe Battery Chargers (Model E33A) can overheat and catch fire. The company has received five reports of fires, including two burn injuries. About 1,400 units were sold online from May 2024 through April 2025.
- 2026-07-09CPSCZhangzhoushi Jingqu Trading Co., Ltd., dba Wonder Stone Toys, of ChinaWonderStone infant walkers recalled for fall hazard
WonderStone infant walkers can fit through standard doorways and fail to stop at the edge of a step, violating the mandatory safety standard for infant walkers. This poses a risk of serious injury or death from falls.
- 2026-07-09CPSCshenzhenshiyuezhangwangluokejiyouxiangongsi (Shenzhen Yuezhang Network Technology Co., Ltd.), doing business as YUEZHANG, of ChinaMoodooy bed rails recalled for entrapment risk
Moodooy adult portable bed rails can trap users between the rail and mattress, creating a serious risk of asphyxiation. The rails also lack required warning labels and don't meet federal safety standards for adult bed rails.
- 2026-07-09CPSCJomani International Inc., of Monterey Park, CaliforniaBBRKIN and MouTec gun safes recalled for unlock risk
The biometric locks on these gun safes can be opened by people who aren't authorized to access them, creating a serious safety risk. The safes were sold on Amazon from 2020 to 2024 and are used to store firearms and valuables.
- 2026-07-09CPSCBest Buy Purchasing LLC, of Richfield, MinnesotaInsignia gas ranges recalled for fire hazard risk
The front knobs on certain Insignia gas ranges can be accidentally turned on by people or pets, creating a risk of fire. Best Buy is offering free knob covers to prevent accidental activation. No injuries have been reported so far.
- 2026-07-09CPSCConair LLC, of Stamford, Connecticut, dba CuisinartCuisinart Propel+ gas grill recalled for glass shatter risk
The tempered glass window on the pizza oven of this grill can shatter during use, creating a laceration hazard. Conair has received 37 reports of the glass shattering and one report of fire; no injuries have been reported so far.
- 2026-07-08FDA-DeviceZimmer Surgical IncClass IIZimmer Surgical tourniquet hoses recalled for sterility breach
Certain sterile tourniquet extension hoses may have a breach in the sealing area of the sterile pouch, which could allow contamination. If used without detection, the hose could potentially cause a moderate localized infection at the surgical site.
- 2026-07-08FDA-DeviceZimmer Surgical IncClass IIBrand Name: Sterile Tourniquet Hoses Product Name: A.T.S¿ 4000 TS Tourniquet Systems Dual Hose with CPC Connectors Model/Catalog Number: 60-1812-101-00 Software Version: N/A Product Description: Dual Sterile Extension Hose with PLC Connector Component: N/A
Potential sterility breach in sealing area of sterile pouch. If used, issue may result in moderate localized infection. If discovered prior to use, may result in clinically insignificant extension of surgery to find another readily available device.
- 2026-07-08FDA-DeviceW L Gore & Associates, Inc.Class IIGORE TAG thoracic endoprosthesis recalled for catheter separation
W L Gore & Associates has recalled specific batches of the GORE TAG Thoracic Branch Endoprosthesis Side Branch Component due to a risk of catheter separation during use. This is a surgical implant used to repair certain aortic conditions. The separation could potentially affect the device's ability to function as intended.
- 2026-07-08FDA-DeviceMasimo CorporationClass IIMasimo Radius VSM cuff recalled for false alarms and rough edges
Masimo Corporation is recalling certain Radius VSM Disposable NIBP Cuff devices due to two issues: the ECG electrode may incorrectly detect abnormal heart rhythms in patients with normal heart rates, triggering false alarms that can distract clinicians; and small and medium-sized blood pressure cuffs may have rough edges that can irritate skin. These issues could delay proper treatment or patient discomfort in healthcare settings.
- 2026-07-08FDA-DeviceMasimo CorporationClass IIMasimo Radius VSM ECG set recalled for false alarms and cuff irritation
Masimo Corporation recalled its Radius VSM ECG pre-connected Set due to two issues: the ECG electrode assembly may incorrectly detect abnormal heart rhythms in patients with normal heart rates, triggering false alarms that can distract clinicians from real patient concerns; and small and medium blood pressure cuffs may have rough edges that can irritate skin.
- 2026-07-08FDA-DeviceLaborie Medical Technologies CorpClass IILaborie Solar GI System recalled for moisture accumulation risk
Laborie Medical Technologies' Solar GI System water perfusion devices may accumulate moisture inside tubing, filters, and pressure sensors during extended clinical use. This moisture buildup can affect how the system measures airflow and pressure, potentially impacting test results.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IIBard Access Systems biopsy trays recalled for defective lidocaine
Bard Access Systems is recalling soft tissue biopsy trays (Models 4380 and 4382A) because the lidocaine ampoules included in the kits were manufactured under deficient manufacturing practices. The affected trays are used by healthcare providers to collect tissue samples from patients.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IIBard Provena Midline Catheters recalled for lidocaine manufacturing defect
Bard Access Systems is recalling certain Provena Midline Catheters because the lidocaine ampoules included with them were manufactured under deficient manufacturing practices. The catheters are used for short-term intravenous therapy, blood sampling, and contrast media injection. The defect affects multiple sizes and configurations across worldwide distribution.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IIBard PowerPICC catheters recalled for lidocaine quality issue
Several models of Bard PowerPICC catheters included lidocaine ampoules (small vials) that were manufactured under deficient manufacturing practices. The lidocaine supplier has issued a recall of these ampoules due to quality concerns.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IIBard Groshong NXT catheter recalled for lidocaine manufacturing defect
Lidocaine ampoules supplied with Bard's Groshong NXT ClearVue Catheter were manufactured under deficient practices. The supplier has initiated a recall of the affected ampoules due to these manufacturing concerns.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IIBard PowerPICC Provena catheters recalled for defective lidocaine
PowerPICC Provena peripheral catheters supplied with lidocaine ampoules manufactured under deficient manufacturing practices. The lidocaine ampoules are being recalled by the supplier due to quality concerns. These catheters are used for intravenous therapy, blood sampling, and central venous pressure monitoring in healthcare settings.
- 2026-07-08FDA-DeviceBard Access Systems, Inc.Class IIBard PowerMidline Catheter recalled for lidocaine manufacturing defect
Bard Access Systems is recalling PowerMidline Catheters (4 Fr Dual-Lumen) because the lidocaine ampoules included with these devices were manufactured under deficient manufacturing practices. The affected catheters were distributed nationwide and internationally.