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 |
|---|---|---|---|---|---|
Autobrush Recalls Sonic Pro Children's Toothbrush Boxes Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries
This recall involves Autobrush's Sonic Pro Kids toothbrush boxes used as packaging for delivering children's toothbrushes. The electric toothbrushes consist of a u-shaped mouthpiece and a plastic base with an animal's face that matches the model's name: Unity the Unicorn, Lenni the Lion, Harley the Hippo and Danny the Dino. The light-up, musical toothbrushes have a built-in timer and three brush settings and were sold with a USB cable, a magnetic plug and decoration stickers inside a cardboard delivery box. The delivery box's white tray has a speaker with a coin cell battery on the underside. Additionally, "autobrush KIDS," the toothbrush's model name and an animal image that corresponds to the model are printed on the box.
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CPSC
10735
|
Child/Baby | High |
Apr 24, 2026
Recall: Apr 23, 2026
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Details |
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Rear Brake Modulators May Short Circuit
Volvo Trucks North America (Volvo Trucks) is recalling certain 2026-2027 VNR (4) and 2025-2027 VNL (4) vehicles. The rear brake modulators may have unprotected electrical connectors that can short circuit and lead to a loss of the anti-lock brake system (ABS) and electronic stability control (ESC). A loss of anti-lock brakes and electronic stability control increases the risk of a crash or injury.
|
NHTSA
26V260000
|
Vehicle | High |
Apr 23, 2026
Recall: Apr 23, 2026
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Details |
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Rear Brake Modulators May Short Circuit
Mack Trucks, Inc. (Mack) is recalling certain 2025-2027 Pioneer (4) and 2026-2027 Anthem (4) vehicles. The rear brake modulators may have unprotected electrical connectors that can short circuit and lead to a loss of the anti-lock brake system (ABS) and electronic stability control (ESC). A loss of anti-lock brakes and electronic stability control increases the risk of a crash or injury.
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NHTSA
26V261000
|
Vehicle | High |
Apr 23, 2026
Recall: Apr 23, 2026
|
Details |
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Instrument Panel Display Failure/FMVSS 108, 208
Chrysler (FCA US, LLC) is recalling certain 2024-2025 Jeep Wagoneer S and Dodge Charger electric vehicles. A software error may cause the instrument panel display to fail. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard numbers 108, "Lamps, Reflective Devices, and Associated Equipment," 126, "Electronic Stability Control Systems for Light Vehicles," 135, "Light Vehicle Brake Systems," 138, "Tire Pressure Monitoring System," and/or 208, "Occupant Crash Protection." An instrument panel display that fails to show critical safety information, such as gear selection and warning lights, increases the risk of a crash.
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NHTSA
26V262000
|
Vehicle | High |
Apr 23, 2026
Recall: Apr 23, 2026
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Details |
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Sediment in Brake Fluid/FMVSS 116
General Motors (GM) is recalling certain containers of ACDelco GMW DOT 3 brake and clutch fluid (lot #01977 091222). The brake fluid may contain visible sediment. As such, this brake fluid fails to conform to Federal Motor Vehicle Safety Standard number 116, "Motor Vehicle Brake Fluids." Sediment in brake fluid may reduce brake performance, increasing the risk of a crash.
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NHTSA
26E025000
|
Vehicle | High |
Apr 23, 2026
Recall: Apr 23, 2026
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Details |
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Fuel Tank May Leak
Jaguar Land Rover North America, LLC (Land Rover) is recalling certain 2026 Land Rover Defender vehicles. The fuel tank was improperly manufactured with walls that are too thin. In the event of a crash, an improperly manufactured fuel tank may leak fuel, increasing the risk of a fire.
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NHTSA
26V263000
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Vehicle | High |
Apr 23, 2026
Recall: Apr 23, 2026
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Details |
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Park Outside: Generator May Turn On Unexpectedly
REV Recreation Group (REV) is recalling certain 2026 Holiday Rambler Vacationer, Admiral, Fleetwood Flair, Fortis, and Bounder motorhomes. The furnace may create electrical signal that turns the generator on unexpectedly. A generator that operates in an enclosed space, such as a garage, increases the risk of injury or death from carbon monoxide poisoning.
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NHTSA
26V264000
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Vehicle | High |
Apr 23, 2026
Recall: Apr 23, 2026
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Details |
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Label is predominantly green with white lettering in a clear plastic clamshell container. Pure Palm dates- Medjool Dates Net Wt. 16OZ UPC: 852160007005
mislabeled Coconut Date Bites. (product is coconut covered, label is for regular date bites)
|
FDA
H-0681-2026
|
Food | High |
Apr 22, 2026
Recall: Apr 1, 2026
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Details |
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Raw & Unfiltered Bee Well Wildflower Honey NET wT. 12 OZ (340g) UPC 8 32587 00003 2, NET WT. 22 OZ (624g) UPC 8 32587 00002 5 & NET WT. 44 OZ (1.25g) UPC 8 32587 00001 8 100% Pure Honey Bee Well Honey 909 W. Main Street Pickens, SC 29671
High sugar content. The firm was notified by the FDA that sample results were positive for a high C4 sugar content.
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FDA
H-0664-2026
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Food | High |
Apr 22, 2026
Recall: Mar 20, 2026
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Details |
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Booey's Dragon's Breath sauce, 15.2oz ringneck glass bottle. UPC on bottle: 7 01936 29222 3. There are 12 bottles per case. Manufactured Exclusively for BOOEYS GOURMET 3924 N. Cannon St. Spokane, WA 99205. Label declares: INGREDIENTS: Contains Soy and Wheat. *** Soy Sauce (Water, Soybeans, Wheat, Salt ***Squid Sauce (Anchovy Extract) ***Sesame Oil***.
Ingredients statement declares Anchovy and Sasame, but Contains statement does not declare Fish (Anchovy) and Sesame.
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FDA
H-0665-2026
|
Food | High |
Apr 22, 2026
Recall: Mar 23, 2026
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Details |
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B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG. Model Number: SL-2010M2096
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
|
FDA
Z-1799-2026
|
Medical Device | High |
Apr 22, 2026
Recall: Mar 19, 2026
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Details |
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B. Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 2.6MM PUMP SEGMENT. Model Number: B3-3632M3705.
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
|
FDA
Z-1802-2026
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Medical Device | High |
Apr 22, 2026
Recall: Mar 19, 2026
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Details |
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Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015.
Increased rate of out-of-specification endotoxin results.
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FDA
Z-1818-2026
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Medical Device | High |
Apr 22, 2026
Recall: Mar 19, 2026
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Details |
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Cytal Wound Matrix 2-Layer 7x10 cm. Product ID: WSM0710.
Increased rate of out-of-specification endotoxin results.
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FDA
Z-1817-2026
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Medical Device | High |
Apr 22, 2026
Recall: Mar 19, 2026
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Details |
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B Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 4.8MM PUMP SEGMENT. Model Number: B3-4630M4705.
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
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FDA
Z-1803-2026
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Medical Device | High |
Apr 22, 2026
Recall: Mar 19, 2026
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Details |
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LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.
The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.
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FDA
Z-1810-2026
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Medical Device | High |
Apr 22, 2026
Recall: Mar 12, 2026
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Details |
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Cytal Burn Matrix 7x10 cm. Product ID: BMM0710.
Increased rate of out-of-specification endotoxin results.
|
FDA
Z-1819-2026
|
Medical Device | High |
Apr 22, 2026
Recall: Mar 19, 2026
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Details |
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B. Braun Hemodialysis Bloodlines, STREAMLINE FRESENIUS FOR DAVITA. Model Number: SL-2000M2095DA.
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
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FDA
Z-1800-2026
|
Medical Device | High |
Apr 22, 2026
Recall: Mar 19, 2026
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Details |
|
B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG DR. Model Number: SL-2010M2096A.
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
|
FDA
Z-1798-2026
|
Medical Device | High |
Apr 22, 2026
Recall: Mar 19, 2026
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Details |
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CENTURION Circumcision Kit, Medline Kit Number/SKU CIT7050F
On lot of Sterile Circumcision Kits was distributed without the required sterilization process and is therefore not sterile.
|
FDA
Z-1824-2026
|
Medical Device | High |
Apr 22, 2026
Recall: Mar 16, 2026
|
Details |
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ARTIS Pheno VE30A and VE40A, Model 10849000
During 3D acquisitions, lighter and darker patient images may be captured, which may result in less accurate 3D reconstruction. The variation of brightness is a result of a constant unregulated medium dose and the angular change of patient diameter caused by rotational acquisition. This may result in unintentional low-dose radiation exposure to a patient.
|
FDA
Z-1814-2026
|
Medical Device | High |
Apr 22, 2026
Recall: Mar 12, 2026
|
Details |
|
Philips Spectral CT on Rails. Model Number: 728334.
Philips has identified three software issues: 1. During a continuous CT (CCT) scan, there is the potential that the Gantry could remain at the current scan position after pressing Go. 2. Potential where the message of Previous Surview Exists Select Previous Surview?
|
FDA
Z-1825-2026
|
Medical Device | High |
Apr 22, 2026
Recall: Mar 7, 2026
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Details |
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B. Barun Hemodialysis Bloodlines, StreamLine Bloodline Long Version, FMC. Model Number: SL-2000M2095L.
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
|
FDA
Z-1801-2026
|
Medical Device | High |
Apr 22, 2026
Recall: Mar 19, 2026
|
Details |
|
Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.
Increased rate of out-of-specification endotoxin results.
|
FDA
Z-1816-2026
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Medical Device | High |
Apr 22, 2026
Recall: Mar 19, 2026
|
Details |
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Brand Name: Elegance¿ Anterior Cervical Plate Product Name: ELEGANCE 1 LEVEL CERVICAL PLATE, ELEGANCE 2 LEVEL CERVICAL PLATE, ELEGANCE 3 LEVEL CERVICAL PLATE, ELEGANCE 4 LEVEL CERVICAL PLATE Model/Catalog Number: See Excel sheet attached named "FDA 5072 Product Information" Software Version: Not applicable Product Description: The Elegance¿Anterior Cervical plate is designed for use as a cervical plate system. It has a shape which restores the intervertebral height and lordosis. The Elegance¿ Anterior Cervical plate consists in a variety of shapes and sizes of cervical plates with rounded corn
Due to a quality issue regarding the presence of burr on the finished cervical plate product.
|
FDA
Z-1821-2026
|
Medical Device | High |
Apr 22, 2026
Recall: Feb 20, 2026
|
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.
This latest recall page combines CPSC, FDA, USDA FSIS and NHTSA data so shoppers do not need to check each agency page separately.
New alerts for toys, furniture, appliances, electronics, baby products, household goods and products with injury, choking, fire or fall hazards.
Recent FDA notices can include Class I, Class II and Class III recalls, market withdrawals, safety alerts, code information and distribution areas.
FSIS alerts cover meat, poultry and egg products, including public health alerts, undeclared allergens, pathogen risks and misbranding issues.
New vehicle, tire, equipment and child-seat campaigns include defect summaries, affected units, remedy notes and NHTSA campaign numbers.
Recent recall pages are date-driven. Use the published date and recall date to understand whether an alert is new, newly classified or recently updated.
Choose food, vehicle, medical device, baby product, electronics, household or consumer product when the latest list is too broad.
Sort by highest risk when checking for urgent problems such as contamination, serious injury hazards, undeclared allergens, fire risks or vehicle safety defects.
Use the detail page and official source link before taking action. Agency notices may include exact lot codes, model ranges, remedy steps and company contacts.
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Some agencies publish or classify a recall after the company began the recall. Use both the published date and recall date when reviewing a notice.
Match the brand, product name, package size, UPC, lot code, best-by date, allergen or contamination issue and distribution area before taking action.
Yes. Use the risk filter or highest-risk sort to surface recalls marked critical or high risk across all official sources.