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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Boston Scientific Cardiac Resynchronization Therapy (CRT)labeled as: 1. VALITUDE CRT-P EL, Model Number U125; 2. VALITUDE CRT-P EL MRI, Model Number U128; 3. VISIONIST CRT-P EL, Model Number U225; 4. VISIONIST CRT-P EL, Model Number U226; 5. VISIONIST CRT-P EL MRI, Model Number U228.
Updated software, Brady software maintenance release 6 (SMR6), is now available for the ACCOLADE" family of pacemakers and cardiac resynchronization therapy pacemakers (CRT-Ps)1 and the advisory population is expanding to include all CRT-P and dual-chamber extended life (DR-EL) devices. Dual chamber modes are specifically indicated for treatment of the following: " Conduction disorders that require restoration of AV synchrony, including varying degrees of AV block " VVI intolerance (i.e., pacemaker syndrome) in the presence of persistent sinus rhythm " Low cardiac output or congestive heart failure secondary to bradycardia
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FDA
Z-1771-2026
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Medical Device | High |
May 6, 2026
Recall: Mar 19, 2026
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Details |
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Philips SmartPath to dStream for 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782145.
The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.
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FDA
Z-1966-2026
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Medical Device | High |
May 6, 2026
Recall: Apr 14, 2026
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Details |
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Brand Name: Genius" Review Station Product Name: Genius" Review Station Display (Barco Monitor) Model/Catalog Number: CMP-01669 Software Version: N/A - not software version specific Component: Yes, the Genius" Review Station is a component of the Genius" Digital Diagnostics System with the Genius" Cervical AI Algorithm cleared under DEN210035.
It was identified that certain devices were being operated outside the validated and FDA-cleared display configuration due to user modification of the manufacturer-installed settings. Modifications included disabling Barco Application Appearance Manager (AAM), altering calibration and compliance parameters, and adjusting additional display-related settings. This field correction is being conducted to restore affected system to the validated configuration and reinforce proper use in accordance with the Operator's Manual.
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FDA
Z-1949-2026
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Medical Device | High |
May 6, 2026
Recall: Mar 23, 2026
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Details |
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Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows: 1. CATARACT PACK, Medline Kit Number/SKU DYNJ48725A; 2. OCULAR PACK, Medline Kit Number/SKU DYNJ64138B; 3. OCULOPLASTY PACK, Medline Kit Number/SKU DYNJ64572A; 4. OCULOPLASTY PACK, Medline Kit Number/SKU DYNJ64572B; 5. MICROSURGERY PACK, Medline Kit Number/SKU DYNJ67284A; 6. BASIC EYE PACK, Medline Kit Number/SKU DYNJ81411A; 7. SMR SINUS PACK, Medline Kit Number/SKU DYNJ84478; 8. FESS/SEPTO PACK, Medline Kit Number/SKU DYNJ85025; 9. PLASTIC EYE PACK, Medline Kit Number/SKU DYNJ89030; 10. NEURO, Medline Kit Nu
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.
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FDA
Z-2037-2026
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Medical Device | High |
May 6, 2026
Recall: Mar 19, 2026
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Details |
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Medline Neuro Sponges, various dimensions, labeled as: 1. Neuro Sponges, Eponges neuro, Neuroesponjas, size 0.25" X 0.25", XR, 10/PK, Medline SKU NEUROSPNG02; 2. Neuro Sponges, Eponges neuro, Neuroesponjas, size 0.5" X 0.5", XR, 10/PK, Medline SKU NEUROSPNG05; 3. Neuro Sponges, Eponges neuro, Neuroesponjas, size 0.5" X 1", XR, LF, 10/PK, Medline SKU NEUROSPNG06; 4. Neuro Sponges, Eponges neuro, Neuroesponjas, size 0.5" X 1.5", XR, LF, 10/PK, Medline SKU NEUROSPNG07; 5. Neuro Sponges, Eponges neuro, Neuroesponjas, size 0.5" X 3", XR, LF, 10/PK, Medline SKU NEUROSPNG09; 6. Neuro Sponges, Eponges
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.
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FDA
Z-2008-2026
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Medical Device | High |
May 6, 2026
Recall: Mar 19, 2026
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Details |
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BD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for microbiologic use
BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems, where gas generating sachets may produce carbon dioxide levels below specification.
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FDA
Z-1982-2026
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Medical Device | High |
May 6, 2026
Recall: Apr 7, 2026
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Details |
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Contact with Drive Belt Pully May Damage and Cause Oil Lines to Leak
Corp. Micro Bird, Inc. (Micro Bird) is recalling certain 2023-2025 G5 transit buses built on a GM chassis and equipped with a second air conditioning compressor kit. The drive belt pulley may contact and damage the the oil lines. A damaged oil like may leak, increasing the risk of a fire in the presence of an ignition source.
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NHTSA
26V286000
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Vehicle | Unknown |
May 6, 2026
Recall: May 6, 2026
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Details |
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Contact with Drive Belt Pully May Damage and Cause Oil Lines to Leak
Corp. Micro Bird, Inc. (Micro Bird) is recalling certain 2023-2026 G5 and 2024 MB II school buses built on a GM chassis and equipped with a second air conditioning compressor kit. The drive belt pulley may contact and damage the the oil lines. A damaged oil like may leak, increasing the risk of a fire in the presence of an ignition source.
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NHTSA
26V287000
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Vehicle | Unknown |
May 6, 2026
Recall: May 6, 2026
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Details |
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Rearview Camera Image May Not Display/FMVSS 111
Tesla, Inc. (Tesla) is recalling certain 2017, 2021-2023 Model 3, 2020-2023 Model Y, 2021-2023 Model S, and Model X vehicles operating software version 2026.8.6. The rearview camera image may be delayed when the vehicle is placed in reverse. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 111, "Rear Visibility." A delayed rearview image reduces the driver's view behind the vehicle, increasing the risk of a crash.
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NHTSA
26V283000
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Vehicle | High |
May 5, 2026
Recall: May 5, 2026
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Details |
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Incorrect Cargo Carrying Capacity on Label
Shyft Group (Shyft) is recalling certain 2025 Utilimaster Velocity vehicles. The incorrect vehicle load value may be listed on the vehicle cargo carrying capacity label. Incorrect weight information may lead to unintentionally overloading the vehicle, increasing the risk of a crash.
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NHTSA
26V284000
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Vehicle | High |
May 5, 2026
Recall: May 5, 2026
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Details |
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Incorrectly Routed LP Hose May Cause Fire
Winnebago Industries, Inc. (Winnebago) is recalling certain 2026-2027 Solis recreational vehicles. The liquid propane (LP) hose may be incorrectly routed over the exhaust heat shield. Heat exposure may damage the hose. A damaged hose may leak fuel, increasing the risk of a fire.
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NHTSA
26V285000
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Vehicle | Unknown |
May 5, 2026
Recall: May 5, 2026
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Details |
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FSIS Issues Public Health Alert for Ravioli Pasta With Beef Sauce Due to Misbranding and Undeclared Allergens
WASHINGTON, May 4, 2026 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for ravioli pasta products due to misbranding and undeclared allergens. The ravioli labeled as beef and burrata may actually contain shrimp filling in lobster sauce. The shrimp and lobster, known allergens (shellfish), are not declared on the product label. FSIS is issuing this public health alert to ensure that consumers with shellfish allergies are aware that this product should not be consumed. A recall was not requested because the product is no longer available for purchase. The ravioli pasta items were produced between March 10, 2026, and April 21, 2026. The following product is subject to the public health alert [ view labels ]: 32-oz. plastic bag packages containing “Giovanni Rana RANA Rustic Beef Sauce & Creamy Burrata Cheese Ravioli” with “use by” dates ranging 05/14/2026 – 06/25/2026. The product bears establishment number “Est. 44870” inside the USDA mark of inspection. These items were shipped to Costco retail stores in Maryland and New Jersey. The problem was discovered when the establishment notified FSIS that they received two consumer complaints reporting the beef sauce and burrata ravioli actually contained shrimp ravioli. There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a health care provider. FSIS is concerned that some product may be in consumers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. Media and consumers with questions regarding the public health alert can contact April Klein, Customer Service Manager, Rana Meal Solutions, at [email protected] . Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to [email protected] . For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/ .
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FSIS
PHA-05042026-01
|
Food | Unknown |
May 4, 2026
Recall: May 4, 2026
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Details |
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Incorrect Load Carrying Capacity on Label/FMVSS 110
Gulf States Toyota, Inc. (GST) is recalling certain 2026 4Runner vehicles. The load carrying capacity modification label states the incorrect load carrying capacity. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 110, "Tire Selection and Rims." An incorrect load carrying capacity label may lead to improper loading of the vehicle, increasing the risk of a crash.
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NHTSA
26V282000
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Vehicle | High |
May 4, 2026
Recall: May 4, 2026
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Details |
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ADS Software May Allow Vehicle to Drive onto a Flooded Roadway
Waymo LLC (Waymo) is recalling certain 5th and 6th Generation Automated Driving Systems (ADS). The software may allow the vehicle to slow and then drive into standing water on higher speed roadways. Entering a flooded roadway can cause a loss of vehicle control, increasing the risk of a crash or injury.
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NHTSA
26E026000
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Vehicle | High |
May 1, 2026
Recall: May 1, 2026
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Details |
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Front Passenger Seat Belt May Not Fasten
Mercedes-Benz USA, LLC (MBUSA) is recalling certain 2026 CLA 350 4MATIC (EV) and CLA 250+ (EV) vehicles. The front passenger seat belt retractor may have been manufactured with a defect that prevents the deactivation of the child seat safety function (Automatic Locking Retractor). As a result, the seat belt may remain in a locked position and cannot be extended. A passenger who is unable to fasten their seat belt is not properly restrained, increasing their risk of injury in a crash.
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NHTSA
26V278000
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Vehicle | High |
May 1, 2026
Recall: May 1, 2026
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Details |
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Speedometer May Fail to Illuminate/FVMSS 101
New Flyer of America, Inc. (New Flyer) is recalling certain 2022 XE40 transit buses. The speedometer may not illuminate when the headlights are turned on. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 101, "Controls and Displays." An unlit speedometer cannot show the vehicle's speed, increasing the risk of a crash.
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NHTSA
26V279000
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Vehicle | High |
May 1, 2026
Recall: May 1, 2026
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Details |
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Rear Bench May Be Missing Seat Legs
Braun Corporation (Braun) is recalling certain 2026 Ram ProMaster vehicles. The rear bench may have only two of four seat legs installed. As such, these vehicles fail to comply with Federal Motor Vehicle Safety Standard number 207, "Seating Systems." An incomplete seat may not properly restrain an occupant, increasing risk of injury during a crash.
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NHTSA
26V280000
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Vehicle | High |
May 1, 2026
Recall: May 1, 2026
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Details |
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Blank Instrument Panel Display
Mercedes-Benz USA, LLC (MBUSA) is recalling certain 2024-2026 AMG GT, C-Class, E-Class, SL, CLE, and GLC vehicles. The infotainment control unit may reset while the vehicle is in motion and cause the instrument panel display to go blank. An instrument panel display that fails to show critical safety information, such as the speedometer and warning lights, increases the risk of a crash.
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NHTSA
26V281000
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Vehicle | High |
May 1, 2026
Recall: May 1, 2026
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Details |
Thermos Recalls 8.2 Million Stainless King Food Jars and Bottles Due to Serious Impact Injury and Laceration Hazards
This recall involves Thermos Stainless King Food Jars with model numbers SK3000 and SK3020, manufactured before July 2023 and all Thermos Sportsman Food & Beverage Bottles with model number SK3010. The stopper of the recalled Food Jars and Food & Beverage Bottles does not have a pressure relief in the center. The containers were sold in a variety of colors in sizes of 16-oz, model number SK3000, 24-oz, model number SK3020, and 40-oz, model number SK3010. The Thermos trademark is located on the side of the product. The model numbers are printed on the bottom of the recalled containers.
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CPSC
10741
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Consumer Product | Medium |
May 1, 2026
Recall: Apr 30, 2026
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Details |
Segmart 4-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violate Mandatory Standard for Clothing Storage Units; Sold on Walmart.com by SOFT
This recall involves Segmart 4-Drawer Dressers. The recalled dressers are made of particle board and were sold in black and white. The dressers have four drawers, are 15.7 inches long by 26 inches wide by 28.5 inches tall and weigh 70 pounds. Model numbers "FFLWM002BK" or "FFLWM002WE" are printed on labels located the product packaging.
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CPSC
10743
|
Child/Baby | High |
May 1, 2026
Recall: Apr 30, 2026
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Details |
Residential Elevators Recalls Elevator StrikeLock Hoistway Door Locking Device Due to Risk of Serious Injury or Death from Fall and Injury Hazards
This recall involves the StrikeLock hoistway door locking device, used to secure a residential elevator hoistway landing door. The product is silver in color. The door locking device is installed into the landing door jamb and looks similar to a standard door latch plate.
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CPSC
10747
|
Consumer Product | High |
May 1, 2026
Recall: Apr 30, 2026
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Details |
Qumeney Bicycle Light Sets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries; Sold on Amazon by Smfanlus
This recall involves Qumeney Bicycle Light Sets, models: BL-01 and BL-02. The bicycle lights are encased in silicone material and available in six colors including: black, white, red, green, yellow and blue. They are sold in packs of six (one of each color) and 24 (four of each color), each light contains two button cell batteries. The bicycle lights have "QUMENEY" printed on the labels located at the top of the package.
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CPSC
10751
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Child/Baby | High |
May 1, 2026
Recall: Apr 30, 2026
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Details |
Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Imported by DGIVOVO US
This recall involves DGIVOVO US-branded pressure washers. The recalled, electric pressure washers are red, green or blue with black, and measure about seven inches high, nine inches wide and eight inches deep. They came with a 500 ml spray can attachment, foam cannon, four connect nozzles, a 20-foot hose and two rollers. "Model: C4012PLUS-1500C" is printed on a label located on the back of the pressure washers.
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CPSC
10749
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Consumer Product | High |
May 1, 2026
Recall: Apr 30, 2026
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Details |
Malker Bicycle Light Sets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Consumer Products with Button Cell Batteries; Sold on Amazon by MalkerDirect
This recall involves Malker Bicycle Light Sets. The bicycle lights were sold in 4- or 8-pack sizes. The products made with red silicone emit red light, products with black silicone emit white light, and products with white silicone emit white light. Each light contains two preinstalled CR2032 button cell batteries. The bicycle lights have "Malker Bicycle Light" printed on labels located on the front packaging. Recalled Bicycle Light Sets: Pack Description Price 8 Piece 4 pcs red & 4 pcs black 9.99 4 Piece 2 pcs red & 2 pcs black $6.99 4 Piece 2 pcs red & 2 pcs white 6.99 4 Piece 4 pcs black $6.99
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CPSC
10744
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Child/Baby | High |
May 1, 2026
Recall: Apr 30, 2026
|
Details |
Earthtec Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Manufactured by Tonyidea
This recall involves Earthtec pool drain covers that are sold for use in swimming pools. The pool drain covers are 7 3/8-inches in diameter and come with two screws. They are white and made of ABS plastic.
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CPSC
10748
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Consumer Product | High |
May 1, 2026
Recall: Apr 30, 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.
High-risk notices often involve serious injury, contamination, undeclared allergens, vehicle crash hazards, fire risks or products that should not be used or consumed.
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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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FSIS alerts cover meat, poultry and egg products, including public health alerts, undeclared allergens, pathogen risks and misbranding issues.
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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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