Product Name Or Brand
Start broad with the product name, manufacturer, retailer brand or model family. This is usually the fastest way to find a possible notice.
Start with the product name or brand. If the list is too broad, search the exact UPC, lot code, model number, date code, NHTSA campaign number or official recall number printed on the notice or label.
Results help you find a possible match quickly. Before you stop use, discard, return or repair anything, open the official notice and confirm every affected detail.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
|
Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Incomplete seals on sterile product
|
FDA
Z-2191-2026
|
Medical Device | High |
May 20, 2026
Recall: Apr 10, 2026
|
Details |
|
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.
|
FDA
Z-2047-2026
|
Medical Device | High |
May 20, 2026
Recall: Mar 25, 2026
|
Details |
|
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.
|
FDA
Z-2167-2026
|
Medical Device | High |
May 20, 2026
Recall: Apr 8, 2026
|
Details |
|
BARD Dynamic Deca Steerable, Product Number 201101; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Incomplete seals on sterile product
|
FDA
Z-2174-2026
|
Medical Device | High |
May 20, 2026
Recall: Apr 10, 2026
|
Details |
|
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.
|
FDA
Z-2136-2026
|
Medical Device | High |
May 20, 2026
Recall: Mar 19, 2026
|
Details |
|
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
|
FDA
Z-2200-2026
|
Medical Device | High |
May 20, 2026
Recall: Apr 6, 2026
|
Details |
|
BARD Dynamic Tip Steerable, Product Number 6DYNTP001;
Incomplete seals on sterile product
|
FDA
Z-2177-2026
|
Medical Device | High |
May 20, 2026
Recall: Apr 10, 2026
|
Details |
|
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.
|
FDA
Z-2153-2026
|
Medical Device | High |
May 20, 2026
Recall: Mar 26, 2026
|
Details |
|
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 |
|
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.
|
NHTSA
26V318000
|
Vehicle | Medium |
May 20, 2026
Recall: May 20, 2026
|
Details |
|
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.
|
NHTSA
26V319000
|
Vehicle | Medium |
May 20, 2026
Recall: May 20, 2026
|
Details |
|
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.
|
NHTSA
26V320000
|
Vehicle | High |
May 20, 2026
Recall: May 20, 2026
|
Details |
|
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.
|
NHTSA
26V321000
|
Vehicle | High |
May 20, 2026
Recall: May 20, 2026
|
Details |
|
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.
|
NHTSA
26V322000
|
Vehicle | High |
May 20, 2026
Recall: May 20, 2026
|
Details |
|
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.
|
NHTSA
26V323000
|
Vehicle | High |
May 20, 2026
Recall: May 20, 2026
|
Details |
|
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.
|
NHTSA
26V324000
|
Vehicle | Unknown |
May 20, 2026
Recall: May 20, 2026
|
Details |
|
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.
|
NHTSA
26E032000
|
Vehicle | High |
May 20, 2026
Recall: May 20, 2026
|
Details |
|
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.
|
NHTSA
26V314000
|
Vehicle | High |
May 19, 2026
Recall: May 19, 2026
|
Details |
|
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.
|
NHTSA
26V315000
|
Vehicle | High |
May 19, 2026
Recall: May 19, 2026
|
Details |
|
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.
|
NHTSA
26V316000
|
Vehicle | High |
May 19, 2026
Recall: May 19, 2026
|
Details |
|
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.
|
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.
|
NHTSA
26V311000
|
Vehicle | High |
May 18, 2026
Recall: May 18, 2026
|
Details |
|
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.
|
NHTSA
26V312000
|
Vehicle | Medium |
May 18, 2026
Recall: May 18, 2026
|
Details |
|
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.
|
NHTSA
26V313000
|
Vehicle | High |
May 18, 2026
Recall: May 18, 2026
|
Details |
|
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/ .
|
FSIS
PHA-04302026-01
|
Food | Medium |
May 15, 2026
Recall: Apr 30, 2026
|
Details |
Use brand, product name, UPC, lot code, best-by date, package size, allergen, contamination issue or distribution state.
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Start broad with the product name, manufacturer, retailer brand or model family. This is usually the fastest way to find a possible notice.
For food, drugs, cosmetics and packaged goods, compare the UPC, lot code, product code, best-by date, use-by date and package size.
For appliances, electronics, toys, furniture and baby products, match the model number, serial range, date code, color, size and retailer listing.
This site can find vehicle recall campaigns. For your exact car, use the official NHTSA VIN lookup to confirm unrepaired recall status.
Consumer products, toys, furniture, appliances, electronics and baby products. CPSC remedy details can change after a notice is first posted.
FDA-regulated foods, drugs, cosmetics and medical devices. FDA notes that not every recall has a press release on the public recalls page.
Meat, poultry and egg product recalls and public health alerts. Check establishment numbers, lot codes, labels and affected states.
Vehicle, tire, equipment and child-seat campaigns. VIN or license plate lookup is needed to know whether your specific vehicle still needs repair.
Use the brand, product name, manufacturer or retailer. If the result list is long, add a code from the label or package.
Read the product description, recall reason, hazard, affected dates, source agency and official recall number before taking action.
Compare the UPC, lot, best-by date, establishment number, model, serial range, color, size, state, retailer and product photo.
The notice may say stop using, do not eat, discard, return for refund, request a repair kit, replace a part or schedule dealer service.
Do not rely on brand alone. Match the package size, UPC, lot code, best-by date, use-by date, distribution states and any allergy or contamination warning.
Look for model number, date code, serial range, color, size, online listing, product photo and the exact hazard such as choking, suffocation, fire or fall risk.
Use campaign results to understand the issue, then verify your VIN, car seat model or tire information with NHTSA or the manufacturer.
Your item may not be part of that specific recall. Check spelling, older notices, retailer alerts and the official source before deciding it is safe.
A product recall is a safety or compliance notice saying a product may need to be corrected, removed, returned, repaired, replaced, refunded or discarded.
If all affected details match, follow the official instructions. Keep packaging, take photos, save receipts and contact the company or retailer when a refund or repair is offered.
A similar brand or product name is not enough. UPCs, lot codes, dates, model numbers, serial ranges and distribution areas determine whether your item is included.
Be careful with text messages, social posts or refund forms that ask for private information. Verify the notice through an official agency, retailer or manufacturer page.
Yes, when the official recall notice includes a UPC or product code. If no result appears, also search the brand, product name, package size, lot code and company name.
Yes. Lot codes are especially useful for food, drug, cosmetic and pet food recalls because only certain production batches may be affected.
No. This tool helps find vehicle recall campaigns and NHTSA numbers. Use the official NHTSA VIN or license plate lookup for vehicle-specific unrepaired recall status.
The database combines multiple official U.S. sources, but agencies and companies can publish or update notices at different times. Always check the linked official notice before taking final action.