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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Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Incomplete seals on sterile product
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FDA
Z-2191-2026
|
Medical Device | High |
May 20, 2026
Recall: Apr 10, 2026
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Details |
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Rolls of label stock used with the Omnicell i.v.Station. 1. Part Number 258920028, LABEL, STERILE, IVSTATION SYRINGE (40MMX40MM). 2. Part Number 258900029, LABEL, STERILE, IVSTATION SYRINGE (20MMX40MM). Model/Catalog Number: IVS-RBT-001. i.v.STATION is an automation device used for preparation and compounding of IV medications, which also applies labels to compounded preparations for identification and traceability.
Potential for mislabeled syringe produced by the i.v.STATION device.
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FDA
Z-2047-2026
|
Medical Device | High |
May 20, 2026
Recall: Mar 25, 2026
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Details |
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SELENIA DIMENSIONS MAMMOGRAPHY SYSTEMS. Model Numbers: SDA-SYS-3000-2D-HTC, SDA-SYS-3000-3D, SDM-SYS-6000-2D, SDM-SYS-6000-3D, SDM-00001-2D, SDM-00001-3D, SDM-00001-M2D, SDM-00001-M3D, SDM-05000-2A2, SDM-05000-2A3, SDM-05000-2AC, SDM-05000-2D2, SDM-05000-2D3, SDM-05000-2DC, SDM-05000-3D2, SDM-05000-3D3, SDM-05000-3DC, SDM-SYS-9000-2D, SDM-SYS-9000-3D.
Complaints have been received of systems developing loose, missing, or broken internal bolts over time.
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FDA
Z-2167-2026
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Medical Device | High |
May 20, 2026
Recall: Apr 8, 2026
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Details |
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BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Incomplete seals on sterile product
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FDA
Z-2174-2026
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Medical Device | High |
May 20, 2026
Recall: Apr 10, 2026
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Details |
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Brand Name: DONJOY Product Name: ICEMAN W/,UNIV,LOOP,NS,EH Model/Catalog Number: 11-1424 Software Version: No Product Description: 11-1424 - ICEMAN W/,UNIV,LOOP,NS,EH The IceMan CLASSIC3¿ cold therapy unit helps reduce pain and swelling, speeding up rehabilitation. The IceMan¿ helps provide extended cold therapy to aid in a variety of indications and protocols as directed by a medical professional. The IceMan CLASSIC3 utilizes DonJoy's recirculation technology. Component: No
Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
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FDA
Z-2136-2026
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Medical Device | High |
May 20, 2026
Recall: Mar 19, 2026
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Details |
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LVIS Intraluminal Support Device, REF/Outside Diameter(OD)xTotal Length(TL)xWorking Length(WL): 214022-CAS/4.0 mm x 22 mm x 18 mm, 214518-CAS/4.5 mm x 18 mm x 14 mm, 213517-CAS/3.5 mm x 17 mm x 13 mm
Stent-assisted coiling device may due to commingling during manufacturing have dimensional nonconformance and/or incorrect device configuration. If device is oversized may lead to increased vessel wall stress, neointimal hyperplasia, vessel injury/rupture; if undersized may lead to incomplete expansion/malposition, acute stent thrombosis, distal embolization, ischemic neurological events
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FDA
Z-2200-2026
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Medical Device | High |
May 20, 2026
Recall: Apr 6, 2026
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Details |
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BARD Dynamic Tip Steerable, Product Number 6DYNTP001;
Incomplete seals on sterile product
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FDA
Z-2177-2026
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Medical Device | High |
May 20, 2026
Recall: Apr 10, 2026
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Details |
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Revolution CT ES, X-ray Computed Tomography, Model Number 5590000-15
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain Revolution Apex, Revolution Ascend, and Revolution CT systems.
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FDA
Z-2153-2026
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Medical Device | High |
May 20, 2026
Recall: Mar 26, 2026
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Details |
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Medline medical convenience kits, containing Namic Manifold, Labeled as: HEART CATH PACK-LF, Medline Kit Number/SKU DYNJ36478B
Medline has identified the presence of particulate within the fluid path of the Manifolds.
|
FDA
Z-2146-2026
|
Medical Device | High |
May 20, 2026
Recall: Mar 24, 2026
|
Details |
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Wheelchair Restraint Retractor May Not Lock
Turtle Top is recalling certain 2026 Terra Transit and Odyssey transit buses. The retractors may not lock, preventing the wheelchair from being properly secured. An unsecured wheelchair can move during transit, increasing the risk of injury.
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NHTSA
26V318000
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Vehicle | Medium |
May 20, 2026
Recall: May 20, 2026
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Details |
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Wheelchair Restraint Retractor May Not Lock
Blue Bird Bus Company (Blue Bird) is recalling certain 2027 Vision school buses. The retractors may not lock, preventing the wheelchair from being properly secured. An unsecured wheelchair can move during transit, increasing the risk of injury.
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NHTSA
26V319000
|
Vehicle | Medium |
May 20, 2026
Recall: May 20, 2026
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Details |
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Debris in Engine May Cause Stall
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2024 Tundra vehicles equipped with a V35A engine. Debris from the manufacturing process may contaminate the engine and cause a main bearing to fail, which can result in an engine stall and loss of drive power. A loss of drive power increases the risk of a crash.
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NHTSA
26V320000
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Vehicle | High |
May 20, 2026
Recall: May 20, 2026
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Details |
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Rearview Camera Image May Not Display/FMVSS 111
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2024 Tiguan vehicles previously repaired under recall 25V082. An error may occur in the camera control unit at vehicle startup, resulting in the rearview camera image not displaying as intended. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 111, "Rear Visibility." A rearview camera that does not display an image can reduce the driver's rear view, increasing the risk of a crash.
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NHTSA
26V321000
|
Vehicle | High |
May 20, 2026
Recall: May 20, 2026
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Details |
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Incorrectly Tightened Shock Bolts
K.Z., Inc. (K.Z.) is recalling certain 2026 Durango 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 for other vehicles, increasing the risk of a crash.
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NHTSA
26V322000
|
Vehicle | High |
May 20, 2026
Recall: May 20, 2026
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Details |
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Missing Conspicuity Tape/FMVSS 108
Wabash National Corporation (Wabash) is recalling certain 2019-2023 Transcraft Platform and 2024-2027 Wabash Platform trailers. The conspicuity tape may not have been installed. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 108, "Lamps, Reflective Devices, and Associated Equipment." Missing conspicuity tape can reduce the visibility of the trailer to other drivers, increasing the risk of a crash.
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NHTSA
26V323000
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Vehicle | High |
May 20, 2026
Recall: May 20, 2026
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Details |
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Battery Heating Pad May Overheat
Alliance RV, LLC (Alliance) is recalling certain 2022-2025 Valor and Paradigm recreational trailers. The heating pad may not be appropriate for lithium battery applications. The heating pad may overheat in the battery compartment, increasing the risk of a fire.
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NHTSA
26V324000
|
Vehicle | Unknown |
May 20, 2026
Recall: May 20, 2026
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Details |
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Incorrectly Tightened Shock Bolts
Lippert is recalling certain Curt Touring Coil Suspensions with part number 298315. 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
26E032000
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Vehicle | High |
May 20, 2026
Recall: May 20, 2026
|
Details |
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Loose Rear Suspension Fasteners
Hyundai Motor America (Hyundai) is recalling certain 2025 Ioniq 5 and 2026 Ioniq 9 vehicles. The fasteners for the rear suspension may loosen and detach, which can result in a loss of vehicle control. A loss of vehicle control increases the risk of a crash.
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NHTSA
26V314000
|
Vehicle | High |
May 19, 2026
Recall: May 19, 2026
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Details |
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Missing Certification Label
Tesla, Inc. (Tesla) is recalling certain 2025-2026 Model Y vehicles. The certification label may not have been installed. As such, these vehicles fail to comply with the requirements of 49 C.F.R. Part 567, "Certification." Missing weight information provided by the label may lead to unintentionally overloading the vehicle, increasing the risk of a crash.
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NHTSA
26V315000
|
Vehicle | High |
May 19, 2026
Recall: May 19, 2026
|
Details |
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Forward Collision Avoidance System May Activate Brakes Unexpectedly
Hyundai Motor America (Hyundai) is recalling certain 2025-2026 Santa Cruz, Tucson, Tucson Hybrid, and Tucson Plug-In Hybrid Electric (PHEV) vehicles. Software in the front cameras may cause the forward collision avoidance system to activate prematurely and unexpectedly apply the brakes. Unexpected braking increases the risk of a crash.
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NHTSA
26V316000
|
Vehicle | High |
May 19, 2026
Recall: May 19, 2026
|
Details |
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Incorrect Reverse and Brake Light Assembly/FMVSS 108
Jerr-Dan Corporation (Jerr-Dan) is recalling certain XLP Carrier kits. The reverse and brake light assemblies may have been installed in the wrong location with the incorrect color or number of lights. As such, the carriers fail to conform to Federal Motor Vehicle Safety Standard (FMVSS) number 108, "Lamps, Reflective Devices and Associated Equipment." Inadequate rear lighting can reduce vehicle visibility or fail to alert other drivers when the vehicle is braking, turning, or reversing, increasing the risk of a crash.
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NHTSA
26E031000
|
Vehicle | High |
May 19, 2026
Recall: May 19, 2026
|
Details |
|
High Voltage Battery Contactor Failure May Cause Loss of Drive Power
Oshkosh Corporation (Oshkosh Defense) is recalling certain 2025 NGDV battery electric vehicles. In cold weather, the high voltage battery contactor may open unexpectedly, causing a loss of drive power. A loss of drive power can increase the risk of a crash.
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NHTSA
26V311000
|
Vehicle | High |
May 18, 2026
Recall: May 18, 2026
|
Details |
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Wheelchair Restraint Retractor May Not Lock
Endera Motors (Endera) is recalling certain 2025-2026 Shuttle transit buses. The retractors may not lock, preventing the wheelchair from being properly secured. An unsecured wheelchair can move during transit, increasing the risk of injury.
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NHTSA
26V312000
|
Vehicle | Medium |
May 18, 2026
Recall: May 18, 2026
|
Details |
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Incorrectly Tightened Shock Bolts
Keystone RV Company (Keystone) is recalling certain 2024 Cougar, 2025-2026 Alpine, 2026 Montana, and Walkabout recreational trailers. The shock bolts may have been incorrectly tightened. Loose shock bolts may cause a loss of vehicle stability, increasing the risk of a crash.
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NHTSA
26V313000
|
Vehicle | High |
May 18, 2026
Recall: May 18, 2026
|
Details |
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FSIS Issues Public Health Alert for Various Meat and Poultry Products Containing FDA-Regulated Dairy Products That Have Been Recalled Due to Possible Salmonella Contamination
Last Updated: This release was last updated on May 15, 2026, to reflect additional affected products and their corresponding labels. WASHINGTON, APRIL 30, 2026 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for meat and poultry products containing FDA-regulated dairy ingredients that may be contaminated with Salmonella . FSIS expects additional downstream products will be identified as this ingredient recall progresses. As more information becomes available, FSIS will update this public health alert. Consumers should check back frequently. The list of products subject to the public health alert are available here , including information such as the establishment numbers and states where the products were distributed. The labels are available here . The problem was discovered when FDA notified FSIS that multiple FSIS-regulated establishments received FDA-regulated ingredients formulated with dry milk powder that had been recalled. Consumption of food contaminated with Salmonella can cause salmonellosis, one of the most common bacterial foodborne illnesses. The most common symptoms of salmonellosis are diarrhea, abdominal cramps, and fever within 6 hours to 6 days after eating the contaminated product. The illness usually lasts 4 to 7 days. Most people recover without treatment. In some persons, however, the diarrhea may be so severe that the patient needs to be hospitalized. Older adults, infants, and persons with weakened immune systems are more likely to develop severe illness. Individuals concerned about an illness should contact their health care provider. 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’ or retailers’ refrigerators or freezers. Consumers who have purchased these products are urged not to consume them. Retailers who have purchased these products are urged not to serve or sell them. These products should be thrown away or returned to the place of purchase. 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-04302026-01
|
Food | Medium |
May 15, 2026
Recall: Apr 30, 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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Match the brand, product name, package size, UPC, lot code, best-by date, allergen or contamination issue and distribution area before taking action.
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