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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Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94965; Cardiopulmonary bypass vascular catheter
Certain lots of product have the potential for a sterile barrier breach.
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FDA
Z-2222-2026
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Medical Device | High |
May 27, 2026
Recall: Apr 21, 2026
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Details |
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Tangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers: (1) TNG4002-IND. (2) TNG-4007-6pk.
Affected devices exhibited fractures at the distal shaft tip without complete detachment.
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FDA
Z-2209-2026
|
Medical Device | High |
May 27, 2026
Recall: Mar 23, 2026
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Details |
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Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 33424 Silastic Brand Foley Catheter 5cc REF: 33614 33616 33618 33620 33622 33624
Due to stain present on the surface of affected foley catheters.
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FDA
Z-2226-2026
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Medical Device | High |
May 27, 2026
Recall: Apr 23, 2026
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Details |
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OneLIF Interbody Cage (REF/Description): 010-107-1007/Small 7 Degree 10mm X 7mm, 010-107-1007-2/Small 7 Degree 10mm X 7mm - Oblique, 010-107-1209/Small 7 Degree 12mm X 9mm, 010-107-1411/Small 7 Degree 14mm X 11mm, 010-107-1613/Small 7 Degree 16mm X 13mm, 010-113-1006/Small, 13 Degree 10mm X 6mm, 010-113-1006-2/Small, 13 Degree, 10mm X 6mm - Oblique, 010-113-1208/Small 13 Degree 12mm X 8mm, 010-113-1410/Small 13 Degree 14mm X 10mm, 010-113-1612/Small 13 Degree 16mm X 12mm, 010-119-1407/19 Degree 14mm X 7mm, 010-119-1609/Small 19 Degree 16mm X 9mm, 010-119-1811/Small 19 Degree 18mm X 11mm, 010-1
Intervertebral body fusion system straight inserter failed to properly attach to affected cages, which may result in an inability to securely engage the implant with the inserter, which could lead to procedural delay and/or the need to select an alternative implant.
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FDA
Z-2213-2026
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Medical Device | High |
May 27, 2026
Recall: Apr 23, 2026
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Details |
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Philips Azurion systems not configured with an optional auxiliary pan handle. Includes the below product descriptions and corresponding model numbers. 1. Azurion 3 M12; Model Numbers: 722063, 722229. 2. Azurion 3 M15; Model Numbers: 722222, 722064, 722280, 722230. 3. Azurion 5 M12; Model Numbers: 722227, 722231. 4. Azurion 5 M20; Model Numbers: 722228, 722232, 722281. 5. Azurion 7 B12; Model Numbers: 722067, 722225, 722235. 6. Azurion 7 B20; Model Numbers: 722068, 722226, 722236. 7. Azurion 7 M12; Model Numbers: 722078, 722223, 722233. 8. Azurion 7 M20; Model Numbers: 722079, 722224, 722234, 7
Potential safety issue with Philips Azurion systems, where longitudinal and transverse table movements may be impacted due to mechanical wear of the Float Tabletop control on the control module.
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FDA
Z-2225-2026
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Medical Device | High |
May 27, 2026
Recall: Apr 28, 2026
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Details |
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Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94915; Cardiopulmonary bypass vascular catheter
Certain lots of product have the potential for a sterile barrier breach.
|
FDA
Z-2221-2026
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Medical Device | High |
May 27, 2026
Recall: Apr 21, 2026
|
Details |
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Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94665; Cardiopulmonary bypass vascular catheter
Certain lots of product have the potential for a sterile barrier breach.
|
FDA
Z-2217-2026
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Medical Device | High |
May 27, 2026
Recall: Apr 21, 2026
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Details |
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Swan-Ganz Pacing Catheter, Models: D200F7;
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.
|
FDA
Z-2204-2026
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Medical Device | High |
May 27, 2026
Recall: Apr 8, 2026
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Details |
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Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T; Cardiopulmonary bypass vascular catheter
Certain lots of product have the potential for a sterile barrier breach.
|
FDA
Z-2214-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 21, 2026
|
Details |
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Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94215T; Cardiopulmonary bypass vascular catheter
Certain lots of product have the potential for a sterile barrier breach.
|
FDA
Z-2216-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 21, 2026
|
Details |
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Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913; Cardiopulmonary bypass vascular catheter
Certain lots of product have the potential for a sterile barrier breach.
|
FDA
Z-2219-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 21, 2026
|
Details |
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Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94725; Cardiopulmonary bypass vascular catheter
Certain lots of product have the potential for a sterile barrier breach.
|
FDA
Z-2218-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 21, 2026
|
Details |
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Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063), Azurion 3 M15 (722064), Azurion 7 B12 (722067), Azurion 7 B20 (722068), Azurion 7 M12 (722078), Azurion 7 M20 (722079, 722224).
The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leakage may affect the cooling performance of the X-ray tube. When the oil flow drops below a certain threshold, the system automatically switches to low-dose fluoroscopy and displays the message Low load fluoroscopy flavor selected: Tube cooler problem . This condition cannot be resolved by restarting the system.
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FDA
Z-2227-2026
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Medical Device | High |
May 27, 2026
Recall: Apr 28, 2026
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Details |
|
Swan-Ganz Jr Catheter, Models: SGPT54, SGPT64P, SGPT755P
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.
|
FDA
Z-2203-2026
|
Medical Device | High |
May 27, 2026
Recall: Apr 8, 2026
|
Details |
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Improperly Tightened Shock Bolts
Ember Recreational Vehicles, INC. (Ember) is recalling certain 2026-2027 Touring Edition 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
26V339000
|
Vehicle | High |
May 27, 2026
Recall: May 27, 2026
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Details |
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Instrument Panel Display Failure/FMVSS 101, 305
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2025 Lexus UX Hybrid, 2024 Lexus GX, Toyota Mirai, and 2024-2025 Toyota Land Cruiser Hybrid vehicles. The instrument panel cluster combination meter may fail to display certain warnings or indicators. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 101, "Control and Displays" and in addition, for the subject Mirai vehicles, FMVSS 305, "Electric-powered vehicles: Electrolyte Spillage and Electrical Shock Protection." An instrument panel display that fails to show critical safety information, such as engine coolant temperature or electrical charge increases the risk of a crash or injury.
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NHTSA
26V341000
|
Vehicle | High |
May 27, 2026
Recall: May 27, 2026
|
Details |
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Incorrectly Colored Cargo Carrying Capacity Label/FMVSS 120
Tiffin Motorhomes, Inc. (Tiffin) is recalling certain 2026-2027 Open Trail, Wayfarer, and 2026 Midas recreational vehicles. The Cargo Carrying Capacity (CCC) label may have been incorrectly printed on a white label. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 120, "Wheels and Rims-Other Than Passenger Cars." The incorrect label color may make it difficult for the operator to locate the loading or tire pressure information, increasing the risk of a crash.
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NHTSA
26V342000
|
Vehicle | High |
May 27, 2026
Recall: May 27, 2026
|
Details |
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Loss of Drive Power from Engine Failure
Ford Motor Company (Ford) is recalling certain 2025-2026 Explorer, Ranger, and Bronco vehicles. The engine may fail, which can result in a loss of drive power. A sudden loss of drive power can increase the risk of a crash.
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NHTSA
26V343000
|
Vehicle | High |
May 27, 2026
Recall: May 27, 2026
|
Details |
|
Seat Belt May Fail to Retract or Extend
Ford Motor Company (Ford) is recalling certain 2018-2022 Expedition and Lincoln Navigator vehicles. The seat belt pretensioner in the driver and/or front passenger seat may inadvertently lock the seat belt, which will not allow the belt to retract or extend. Seat belts that do not retract or extend can fail to restrain an occupant as intended, increasing the risk of injury in a crash.
|
NHTSA
26V344000
|
Vehicle | High |
May 27, 2026
Recall: May 27, 2026
|
Details |
|
Incorrect Tire and Weight Capacity Information/FMVSS 110
Ford Motor Company (Ford) is recalling certain 2026 Ranger and Bronco vehicles. The vehicle specifications listed on the tire placard and safety certification labels may be incorrect, including the VIN, capacity weight, seating capacity, front and rear gross axle weight rating (GAWR), tire and rim dimensions, and recommended cold tire pressure. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 110, "Tire Selection and Rims" and 49 CFR Part 567, "Certification." The incorrect tire size, tire pressures, and GAWR listed on the labels can allow the vehicle to be overloaded or have improperly inflated tires, increasing the risk of a crash.
|
NHTSA
26V335000
|
Vehicle | High |
May 26, 2026
Recall: May 26, 2026
|
Details |
|
Incorrectly Tightened Shock Bolts
Forest River, Inc. (Forest River) is recalling certain 2026 Riverstone, Cedar Creek, and 2024 R-Pod recreational trailers equipped with 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 for other vehicles, increasing the risk of a crash.
|
NHTSA
26V336000
|
Vehicle | High |
May 26, 2026
Recall: May 26, 2026
|
Details |
|
Incorrectly Tightened Shock Bolts
Alliance RV, LLC (Alliance) is recalling certain 2025-2027 Paradigm 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 to other vehicles, increasing the risk of a crash.
|
NHTSA
26V337000
|
Vehicle | High |
May 26, 2026
Recall: May 26, 2026
|
Details |
|
Park Outside: Fuel Tank Puncture May Cause Fire
Tiffin Motorhomes, Inc. (Tiffin) is recalling certain 2025-2026 GT1, 2026 GH2, and GH1 motorhomes. A screw may have punctured the fuel tank during manufacturing, causing a fuel leak. A fuel leak in the presence of an ignition source, increases the risk of a fire.
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NHTSA
26V338000
|
Vehicle | High |
May 26, 2026
Recall: May 26, 2026
|
Details |
PandaEar Recalls Portable Hook-On Chairs Due to Risk of Serious Injury or Death from Fall Hazard; Violates Mandatory Standard for Portable Hook-On Chairs
This recall involves two models of PandaEar portable hook-on chairs. The chairs are used to seat young children at the dining table. The chairs contain a black or gray metal frame covered with black, gray, or blue (dinosaur theme) polyester and cotton material and an attached restraint in the occupant seating area. There are two metal arms with plastic covers on top that anchor to a dining table, and the child is suspended from the table. "Panda Ear" can be found on a label stitched to the side of the fabric seats. "Model C2102" can be found on a label located on the bottom of the fabric seats. There are no markings on the product for model BTC-51.
|
CPSC
10784
|
Consumer Product | High |
May 26, 2026
Recall: May 21, 2026
|
Details |
Orb Funkee Squeeze Toys Recalled Due to Risk of Serious Injury or Death from Asbestos Exposure; Imported by The Orb Factory
This recall involves two models of Orb Funkee squeeze toys with the date code 3102491A. The products are made of a soft, stretchable material and filled with sand. Model 17451 is a large golden monkey (stylized "monkee"), and model 41929 is an assortment of small "monkees" in various colors, including orange, purple and green. The date code can be found on the hand of the golden monkee or the back of the smaller monkees.
|
CPSC
10782
|
Consumer Product | High |
May 26, 2026
Recall: May 21, 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.
The site syncs official recall sources daily and stores updated records by source agency, dataset and official recall ID.
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.