Product Recalls Today
Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.
Track recent product recall alerts from official U.S. sources. Filter by recall date, source agency, risk level and product category to find newly published food, vehicle, baby product, medical device and consumer product recalls.
Search recent recall notices by product name, brand, UPC, lot code, model number, source agency or official recall number.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
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RelayPro Thoracic Stent-Graft System (various sizes) Reference numbers: 28-N4-32-104-32U 28-N4-32-164-28U 28-N4-32-164-32U 28-N4-32-209-28U 28-N4-32-209-32U 28-N4-32-259-32U 28-N4-34-109-34U 28-N4-34-154-30U 28-N4-34-154-34U 28-N4-34-209-30U 28-N4-34-209-34U 28-N4-34-259-34U 28-N4-36-109-36U 28-N4-36-154-32U 28-N4-36-154-36U 28-N4-36-199-32U 28-N4-36-199-36U 28-N4-36-259-36U 28-N4-38-109-38U 28-N4-38-154-34U 28-N4-38-154-38U 28-N4-38-199-34U 28-N4-38-199-38U 28-N4-38-259-38U 28-N4-40-114-40U 28-N4-40-154-36U 28-N4-40-154-40U 28-N4-40-204-36U 28-N4-40-204-40U 28-N4-40-259-40U 28-N4-42-114-42U 2
Labeling update concerning proximal clasp disconnection from the outer control tube which may prevent stent graft from being released from the delivery system.
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FDA
Z-2160-2026
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Medical Device | High |
Jun 3, 2026
Recall: Apr 22, 2026
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Details |
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Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) ANESTHESIA TRAY, Medline SKU DYNJRA1355A; 2) SPINAL ANESTHESIA TRAY, Medline SKU DYNJRA2151.
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.
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FDA
Z-2231-2026
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Medical Device | High |
Jun 3, 2026
Recall: Apr 10, 2026
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Details |
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Medline medical convenience kit labeled as EYE TRAY-LF, Medline Kit SKU DYNJ21627P
Specific Medline Kits contain Cardinal Health Monoject 1mL Luer Lock Syringes, Tuberculin Print, Sterile. Cardinal Health has recalled these syringes because the outer carton and blister pack are labeled as a 1 mL Luer Lock Tuberculin Syringe (Product Code 1180100777), but the syringes inside are U-100 insulin syringes.
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FDA
Z-2260-2026
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Medical Device | High |
Jun 3, 2026
Recall: Apr 10, 2026
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Details |
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Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL TRAY W/PENCIL POINT NDL, Medline Kit SKU DYNJRA0245; 2) SPINAL TRAY W/PENCIL POINT NDL, Medline Kit SKU DYNJRA0555; 3) SPINAL TRAY, Medline Kit SKU DYNJRA0836A; 4) SPINAL TRAY, Medline Kit SKU DYNJRA0978A; 5) TRAY, SPINAL, WHIT 24GX4, Medline Kit SKU DYNJRA1034; 6) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKU DYNJRA9028; 7) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA9030.
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.
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FDA
Z-2233-2026
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Medical Device | High |
Jun 3, 2026
Recall: Apr 10, 2026
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Details |
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Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL ANESTHESIA TRAY-LF, Medline Kit SKU DYNJRA0102A; 2) SPINAL TRAY-LF, Medline Kit SKU DYNJRA0143B; 3) SPINAL PREP TRAY-LF, Medline Kit SKU DYNJRA0205B; 4) SPINAL TRAY, Medline Kit SKU DYNJRA0255B; 5) SPINAL TRAY, Medline Kit SKU DYNJRA0320; 6) SPINAL TRAY, Medline Kit SKU DYNJRA0320A; 7) SPINAL BLOCK TRAY- LF, Medline Kit SKU DYNJRA0413C; 8) SPINAL TRAY, Medline Kit SKU DYNJRA0461D; 9) 25G SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA0945; 10) SPINAL TRAY, Medline Kit SKU DYNJRA1140B; 11) SPINAL TRAY,
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.
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FDA
Z-2237-2026
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Medical Device | High |
Jun 3, 2026
Recall: Apr 10, 2026
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Details |
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Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: SPINAL BLOCK 22G QUINCKE 5S BU, Medline Kit SKU DYNJRA9026
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.
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FDA
Z-2235-2026
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Medical Device | High |
Jun 3, 2026
Recall: Apr 10, 2026
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Details |
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GE HealthCare ApexPro v6.0 eDelivery Software, REF #5700026, Product Code SUV; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).
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FDA
Z-2247-2026
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Medical Device | High |
Jun 3, 2026
Recall: Apr 24, 2026
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Details |
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Automated Impella Controller (AIC) with the below product descriptions and corresponding Product Codes. 1. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 2. Impella Controller, Packaged, EU; Product Code: 0042-0000-EU. 3. Impella Controller, Packaged, UK; Product Code: 0042-0000-UK. 4. Impella Controller, Packaged, US; Product Code: 0042-0000-US.
Retrospective submission for following issues identified: 1. Alarm failures, power-path faults, electrical-short risks, and inaccurate motor-current sensing were identified in certain AIC consoles. 2. There is improper alignment between the purge cassette and the motor drive in the AIC. This can result in a piston block event and lead to the inability to complete priming of the purge system, requiring the user to switch to backup AIC console.
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FDA
Z-2238-2026
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Medical Device | High |
Jun 3, 2026
Recall: Jan 17, 2011
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Details |
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Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA1097; 2) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA1154; 3) SPINAL TRAY, Medline Kit SKU DYNJRA1192A; 4) BLOCK TRAY, Medline Kit SKU DYNJRA1212; 5) SPINAL NEEDLE TRAY, Medline Kit SKU DYNJRA1285; 6) SPINAL BLOCK TRAY WHITACRE 24G, Medline Kit SKU DYNJRA9031; 7) SPINAL BLOCK TRAY 25G WHITACRE, Medline Kit SKU DYNJRA9032; 8) 25G SPINAL TRAY, Medline Kit SKU PAIN1239.
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.
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FDA
Z-2236-2026
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Medical Device | High |
Jun 3, 2026
Recall: Apr 10, 2026
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Details |
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Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) BLOCK TRAY, Medline Kit SKU DYNJRA1181C; 2) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKu DYNJRA1860.
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing data integrity concerns and reported efficacy complaints.
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FDA
Z-2234-2026
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Medical Device | High |
Jun 3, 2026
Recall: Apr 10, 2026
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Details |
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GE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603-902, Product Code KSA; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).
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FDA
Z-2246-2026
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Medical Device | High |
Jun 3, 2026
Recall: Apr 24, 2026
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Details |
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False Taillight Warning Light on Instrument Panel Display/FMVSS 101
Jayco, Inc. (Jayco) is recalling certain 2026 Entegra Qwest and Jayco Melbourne Prestige recreational vehicles. The taillight warning light may incorrectly illuminate on the instrument panel display when the taillights are functioning correctly. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 101, "Controls and Displays." The incorrect warning light may fail to alert the driver to critical safety information or cause confusion, increasing the risk of a crash.
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NHTSA
26V360000
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Vehicle | High |
Jun 3, 2026
Recall: Jun 3, 2026
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Details |
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False Taillight Warning Light on Instrument Panel Display/FMVSS 101
Jayco, Inc. (Jayco) is recalling certain 2026 Entegra Qwest SE, Condor, Jayco Granite Ridge, and Melbourne recreational vehicles. The taillight warning light may incorrectly illuminate on the instrument panel display when the taillights are functioning correctly. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 101, "Controls and Displays." The incorrect warning light may fail to alert the driver to critical safety information or cause confusion, increasing the risk of a crash.
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NHTSA
26V361000
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Vehicle | High |
Jun 3, 2026
Recall: Jun 3, 2026
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Details |
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Low Brake Air Pressure Warning Light May Not Illuminate/FMVSS 121
Nova Bus (US) Inc. (Nova Bus) is recalling certain 1997-2002, 2005-2024 LFS and 2009-2024 LFS Artic transit buses. The low brake air pressure warning light may fail to illuminate when the engine is off. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 121, "Air Brake Systems." A low brake air pressure warning light that fails to illuminate when the engine is off will not alert the driver to a low brake pressure condition, increasing the risk of a crash if the parking brake is disengaged before starting the engine.
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NHTSA
26V355000
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Vehicle | High |
Jun 2, 2026
Recall: Jun 2, 2026
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Details |
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Driver Seat Belt Strap May Not Extend/FMVSS 209
Kia America, Inc (Kia) is recalling certain 2027 Telluride and Telluride Hybrid vehicles. The driver seat belt emergency locking retractor may lock, causing the seat belt strap not to extend. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 209, "Seat Belt Assemblies." A seat belt strap that does not extend can fail to restrain an occupant in a crash, increasing the risk of injury.
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NHTSA
26V356000
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Vehicle | High |
Jun 2, 2026
Recall: Jun 2, 2026
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Details |
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Wheelchair Seat Belts May Not Properly Restrain Occupants
Braun Corporation (Braun) is recalling certain 2026 Ram ProMaster vehicles equipped with Q'Straint's One-Combo Belt, with part number TX11258-BA. The wheelchair seat belts may have incompatible connectors and fail to properly restrain occupants. Improperly restrained occupants have an increased risk of injury during a crash.
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NHTSA
26V357000
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Vehicle | High |
Jun 2, 2026
Recall: Jun 2, 2026
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Details |
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Air Bags May Not Deploy
Braun Corporation (Braun) is recalling certain 2023-2026 Chrysler Pacifica and Voyager vehicles. The spring inside the front seat harness connector may contact electrical terminals. The unintended connection may prevent the air bags from deploying, increasing the risk of injury during a crash.
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NHTSA
26V358000
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Vehicle | High |
Jun 2, 2026
Recall: Jun 2, 2026
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Details |
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Incorrectly Tightened Shock Bolts
Grand Design RV, LLC (Grand Design) is recalling certain 2025-2026 Reflection fifth wheel recreational trailers, equipped with certain Curt Touring Coil Suspensions. The shock bolts may have been incorrectly tightened. Broken shock retainer bolt heads and washers may detach and become a road hazard, increasing the risk of a crash.
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NHTSA
26V354000
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Vehicle | High |
Jun 1, 2026
Recall: Jun 1, 2026
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Details |
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Rear Seat Belt Bolts Not Tightened Properly
Mercedes-Benz USA, LLC (MBUSA) is recalling certain 2026 AMG GLS 63 4MATIC+, AMG GLE 63 S 4MATIC+ COUPE, AMG GLE 63 S 4MATIC+, AMG GLE 53 4MATIC+ COUPE, AMG GLE 53 4MATIC+, GLE 450 4MATIC COUPE, GLE 350 4MATIC, Maybach GLS 600 4MATIC, GLS 580 4MATIC, GLS 450 4MATIC, GLE 580 4MATIC, GLE 450E 4MATIC, GLE 450 4MATIC, and GLE 350 vehicles. The bolts for the rear seat belts may not be tightened properly. A loose seat belt may not properly restrain an occupant during a crash, increasing the risk of injury.
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NHTSA
26V353000
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Vehicle | High |
May 29, 2026
Recall: May 29, 2026
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Details |
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Moonroof Glass May Detach
Subaru of America, Inc. (Subaru) is recalling certain 2026 Forester and Forester Hybrid vehicles. The sliding glass panel of the power moonroof assembly may have been improperly bonded to the sliding frame, allowing the glass panel to detach from the vehicle. A detached glass panel may become a road hazard, increasing the risk of a crash.
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NHTSA
26V346000
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Vehicle | High |
May 28, 2026
Recall: May 28, 2026
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Details |
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Incorrect Gear May Be Selected
General Motors, LLC (GM) is recalling certain 2026 Chevrolet Express and GMC Savana vehicles. The gear shifter may provide inaccurate gear selection feedback to the driver due to an incorrectly manufactured steering column assembly. Inaccurate gear selection may result in unexpected vehicle movement, increasing the risk of a crash.
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NHTSA
26V345000
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Vehicle | High |
May 28, 2026
Recall: May 28, 2026
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Details |
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Drive Motor May Detach
International Motors, LLC (International) is recalling certain 2026-2027 IC Bus EVSB school buses. The mounting bracket bolts may have been improperly tightened, allowing the drive motor to detach. A detach drive motor can become a road hazard for other vehicles, increasing the risk of a crash or injury.
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NHTSA
26V348000
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Vehicle | High |
May 28, 2026
Recall: May 28, 2026
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Details |
Walmart Recalls Mainstays 9-Drawer Fabric Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units
This recall involves Mainstays-branded dressers. The fabric dressers have a black metal frame and nine brown or black fabric drawers with handles. The dressers measure about 40 inches long, 13.75 inches wide and 45 inches tall and weigh 32 pounds and were manufactured from September 2023 through December 2025. The Tracking/Lot and the manufacture date in MM/YYYY format are printed on a label under the dresser's top panel of the dresser. "Mainstays 9-Drawer Fabric Dresser" is printed on the product order receipt and packaging.
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CPSC
10796
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Child/Baby | High |
May 28, 2026
Recall: May 28, 2026
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Details |
Missry Associates Recalls Misco Sports Light-Up Racket Sets Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys
This recall involves the Misco Sports Light-Up Racket Set, model MT2287. The set includes two black rackets, one ball and one shuttlecock. "MT2287" and "100125" are printed on the racket handle in white letters.
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CPSC
10794
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Child/Baby | High |
May 28, 2026
Recall: May 28, 2026
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Details |
MiniWarGaming and Primal Horizon Disc Magnets Recalled Due to Risk of Serious Injury or Death from Ingestion; Violate Mandatory Standard for Magnets; Imported by MiniWarGaming
This recall involves MiniWarGaming and Primal Horizon Disc Magnets with the product codes listed in the chart below. The disc magnets are silver and measure between 1/16" to ½" wide by 1/32" to 3/32" high. The Primal Horizon disc magnets were sold in clamshells and have the size and quantity printed on the front of the package and the product code printed on the back of the package. Brand SKU# Size Packaging MiniWarGaming MWGMAG_116_132 1/16" x 1/32" Plastic Bag or Clamshell MiniWarGaming MWGMAG_12_116 ½" x 1/16" Plastic Bag or Clamshell MiniWarGaming MWGMAG_14_116 ¼" x 1/16" Plastic Bag or Clamshell MiniWarGaming MWGMAG_18_116 1/8" x 1/16" Plastic Bag or Clamshell MiniWarGaming MWGMAG_316_116 3/16" x 1/16" Plastic Bag or Clamshell MiniWarGaming MWGMAG_332_116 3/32" x 1/16" Plastic Bag or Clamshell MiniWarGaming MWGMAG_38_116 3/8" x 1/16" Plastic Bag or Clamshell MiniWarGaming MWGMAG_316_332 3/16" x 3/32" Plastic Bag or Clamshell MiniWarGaming MWGMAG_14_332 ¼" x 3/32" Plastic Bag or Clamshell MiniWarGaming MWGMAG_38_332 3/8" x 3/32" Plastic Bag or Clamshell MiniWarGaming MWGMAG_MEGA Various Sizes Plastic Bag or Clamshell Primal Horizon PH10001 1/16" x 1/32" Clamshell Primal Horizon PH10002 3/32" x 1/16" Clamshell Primal Horizon PH10003 1/8" x 1/16" Clamshell Primal Horizon PH10004 3/16" x 1/16" Clamshell Primal Horizon PH10005 ¼" x 1/16" Clamshell Primal Horizon PH10006 3/8" x 1/16" Clamshell Primal Horizon PH10007 Various Sizes Clamshell Primal Horizon PH10008 ½" x 1/16" Clamshell Primal Horizon PH10009 3/16" x 3/32" Clamshell Primal Horizon PH10010 ¼" x 3/32" Clamshell Primal Horizon PH10011 3/8" x 3/32" Clamshell Primal Horizon PH10201 1/16" x 1/32" Clamshell Primal Horizon PH10202 3/32" x 1/16" Clamshell Primal Horizon PH10203 1/8" x 1/16" Clamshell Primal Horizon PH10204 3/16" x 1/16" Clamshell Primal Horizon PH10210 Various Sizes Clamshell Primal Horizon PH10301 Various Sizes Clamshell
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CPSC
10788
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Child/Baby | High |
May 28, 2026
Recall: May 28, 2026
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Details |
Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.
Recent recalls can include new notices, updated classifications, expanded lots, changed risk levels and public health alerts. Sort by newest first for the live recall feed view.
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New alerts for toys, furniture, appliances, electronics, baby products, household goods and products with injury, choking, fire or fall hazards.
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Choose food, vehicle, medical device, baby product, electronics, household or consumer product when the latest list is too broad.
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