Product Recall Checker | Search Product Recalls by UPC, Lot Code, Brand or Model

Latest Product Recall Matches

Showing 2,551 - 2,575 of 4,975 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Bicycle Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets; Sold on Amazon by Gudook Outdoor Sports This recall involves Gudook-branded bicycle helmets, model KY-055. The helmets were sold in blue with white and in size medium (M), fitting a head circumference of about 21.3 to 22.4 inches. The helmets have red padding, black straps, a black and red buckle and a black fit-adjusting knob at the back. Only helmets with batch number 202503 and manufacture date of March 2025 are included in this recall. "Gudook" is printed on the side of the helmet. The model, batch number and manufacture date, in MM/YYYY format, are printed on a label on the inside of the helmet.	CPSC 10801	Consumer Product	High	Jun 5, 2026 Recall: Jun 4, 2026	Details
Park Outside: Battery May Catch Fire Chrysler (FCA US, LLC) is recalling certain 2020-2022 Pacifica Plug-In Hybrid Electric (PHEV) vehicles. The battery pack may cause a vehicle fire, even when the vehicle is parked with the ignition in the "Off" position. A vehicle fire increases the risk of injury.	NHTSA 26V362000	Vehicle	High	Jun 4, 2026 Recall: Jun 4, 2026	Details
Park Outside: Power Steering Wiring May Catch Fire Chrysler (FCA US, LLC) is recalling certain 2021-2025 Jeep Wrangler, Wrangler 4XE, and Jeep Gladiator vehicles. The electric hydraulic power steering pump wiring may overheat and cause a vehicle fire, even when the vehicle is parked with the ignition in the "Off" position. A vehicle fire increases the risk of injury.	NHTSA 26V363000	Vehicle	High	Jun 4, 2026 Recall: Jun 4, 2026	Details
Wheelchair Restraint Retractor May Not Lock International Motors, LLC (International) is recalling certain 2027 IC Bus CESB 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 26V364000	Vehicle	Medium	Jun 4, 2026 Recall: Jun 4, 2026	Details
Tire Repair Kit Bottle Cap May Detach Honda (American Honda Motor Co.) is recalling certain 2023-2026 CR-V Hybrid, Accord Hybrid, and 2025-2026 CR-V Fuel Cell EV vehicles. When using the tire repair kit, pressure may build within the sealant bottle, causing the bottle cap to detach. A detached bottle cap can become a projectile and strike the user or others nearby, increasing the risk of injury.	NHTSA 26V366000	Vehicle	Medium	Jun 4, 2026 Recall: Jun 4, 2026	Details
Rear Suspension Components May Fail American Honda Motor Company (Honda) is recalling certain 2016-2022 Honda Pilot, 2017-2023 Ridgeline, 2019-2023 Passport, and 2014-2020 Acura MDX vehicles that were sold in Connecticut, Delaware, District of Columbia, Illinois, Indiana, Iowa, Kentucky, Maine, Maryland, Massachusetts, Michigan, Minnesota, Missouri, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, Rhode Island, Vermont, Virginia, West Virginia, or Wisconsin. The rear subframe may corrode at the suspension mounting points, which can result in rear suspension component failure. Failure of rear suspension components, such as the rear control arm, can cause a loss of vehicle handling and control, increasing the risk of a crash or injury.	NHTSA 26V365000	Vehicle	High	Jun 4, 2026 Recall: Jun 4, 2026	Details
Fly By Jing (branded) Creamy Sesame Noodles; 3.8 oz packets. Sold in single and 4 packs. Single UPC: 8-50052-23988-6 4 pack UPC: 8-50052-23991-6 Possible cross-contamination resulting in undeclared allergen ingredient (Peanut)	FDA H-0854-2026	Food	High	Jun 3, 2026 Recall: May 8, 2026	Details
Wawa Fruit Punch Pint (16oz), Plastic bottle Undeclared Milk Allergen,	FDA H-0858-2026	Food	High	Jun 3, 2026 Recall: Apr 2, 2026	Details
Wawa Iced Tea Lemon 16 oz Pint, Plastic bottle Undeclared Milk Allergen,	FDA H-0855-2026	Food	High	Jun 3, 2026 Recall: Apr 2, 2026	Details
Parmesan & Herb Bagel Crisps, Item Number 18139, Net Weight: 10 lbs. Legacy Bakehouse, LLC, N8W22100 Johnson Dr., Waukesha, WI 53166. Products were made with recalled California Dairies milk powder due to Salmonella.	FDA H-0851-2026	Food	High	Jun 3, 2026 Recall: May 5, 2026	Details
giant eagle Baked Pita Chips with Parmesan, Garlic & Herb Bagel Crisps, Net Wt 7.33 oz. Shipping Case: 12 ct - 7.33 oz Bags Net Weight: 5.49 lbs. Legacy Bakehouse, LLC, Waukesha WI 53186. Products were made with recalled California Dairies milk powder due to Salmonella.	FDA H-0852-2026	Food	High	Jun 3, 2026 Recall: May 5, 2026	Details
(BULK) SPL-BEV Banana CWT (Banana Smoothie); Super Sack Tote Item# 355-0099 Firm received and used potentially contaminated (Salmonella) ingredient to manufacture various products.	FDA H-0849-2026	Food	High	Jun 3, 2026 Recall: Apr 21, 2026	Details
Wawa Diet Lemonade Pint (16oz), Plastic bottle Undeclared Milk Allergen,	FDA H-0857-2026	Food	High	Jun 3, 2026 Recall: Apr 2, 2026	Details
Wawa Diet Iced Tea Lemon Pint (16oz),Plastic bottle Undeclared Milk Allergen,	FDA H-0856-2026	Food	High	Jun 3, 2026 Recall: Apr 2, 2026	Details
Butter Parsley Bagel Crisps, Item Number 18490, Net Weight: 10 lbs. Legacy Bakehouse, LLC, N8W22100 Johnson Dr., Waukesha, WI 53166. Products were made with recalled California Dairies milk powder due to Salmonella.	FDA H-0850-2026	Food	High	Jun 3, 2026 Recall: May 5, 2026	Details
Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002; Stimulator, electrical, implanted, for parkinsonian tremor A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.	FDA Z-2241-2026	Medical Device	High	Jun 3, 2026 Recall: May 13, 2026	Details
GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL, REF #2063702-101, Product Code SS9; used in conjunction with ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).	FDA Z-2242-2026	Medical Device	High	Jun 3, 2026 Recall: Apr 24, 2026	Details
GE HealthCare APEXPRO v5.0 - ARK2250 - Software Disaster Recovery USB Kit - Orderable by GE Service only, REF #2108523-01; ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).	FDA Z-2243-2026	Medical Device	High	Jun 3, 2026 Recall: Apr 24, 2026	Details
GE HealthCare IOU ASSY ARK2250 CARESCAPE TELEMETRY SERVER, REF #2108729-901, Product Code SS9; ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).	FDA Z-2244-2026	Medical Device	High	Jun 3, 2026 Recall: Apr 24, 2026	Details
Automated Impella Controller (AIC); Product Code: 0042-0000-US; A retrospective review identified that there are AIC units requiring specific hardware updates to address potential safety concerns. These hardware updates have been implemented through Abiomed s servicing process; therefore, AICs that have not received service are pending these updates. Issue 1: The proximity of the internal Video Graphics Array cable to the Digital Signal Processor chipset on the Impellatronic printed circuit assembly could potentially result in Electrostatic Discharge coupling into the Digital Signal Processor which may interrupt motor controls. Issue 2: There is a potential for the Compact Flash Memory Card dislodgement due to external applied forces, which could result in AIC startup failures and data logging issues. Issue 3: Improper routing of the fan wire within the AIC could lead to fan wire damage, which may result in console boot-up failure. Issue 4: Potential capacitor related issues on the Power Battery Manager, including the potential for the capacitors to cause pump stop, purge stop, and/or single fan fuse failures.	FDA Z-2211-2026	Medical Device	High	Jun 3, 2026 Recall: Apr 20, 2026	Details
HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3 Incorrect inner package labeling. Boxes labeled 4010-02-15-T3 markers may contain individual packages labeled as T4 Markers.	FDA Z-2239-2026	Medical Device	High	Jun 3, 2026 Recall: Apr 24, 2026	Details
Allura system; System Code Description (Model Numbers): Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10 OR Table (722022, 722033), Allura Xper FD10/10 (722005, 722011, 722027), Allura Xper FD20 (722006, 722012, 722028), Allura Xper FD20 Biplane (722008, 722013), Allura Xper FD20 OR Table (722015, 722023, 722035), Allura Xper FD20 Biplane OR Table (722025), Allura Xper FD20/10 (722029), Allura Xper FD20/15 (722058), Allura Xper FD20/15 OR Table (722059), Allura Xper FD20/20 (722038), Allura Xper FD20/20 OR Table (722039); It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service. Issues with an HDD may, depending on the specific system PC in which the affected HDD is installed, result in loss of imaging functionality. Additionally, in Allura systems, this may lead to loss of motorized movement, or loss of data. In some cases, a system restart may temporarily restore functionality.	FDA Z-2259-2026	Medical Device	High	Jun 3, 2026 Recall: Apr 30, 2026	Details
GE HealthCare CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603, Product Code KSA; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) GE HealthCare has become aware of an unlikely situation where potential loss of ECG and SpO2 monitoring involving ApexPro CARESCAPE Telemetry Server (CTS) v5.0 and v6.0, can result from a persistent NO COMM or OFF NETWORK condition at the CARESCAPE Central Station or CIC Pro Clinical Information Center (Central Station).	FDA Z-2245-2026	Medical Device	High	Jun 3, 2026 Recall: Apr 24, 2026	Details
Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.), 48775 (Xl) Nitrile Exam Glove failed to meet specifications chemical permeation performance.	FDA Z-2230-2026	Medical Device	High	Jun 3, 2026 Recall: Apr 13, 2026	Details
Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M15 (722064, 722222), Azurion 5 M12 (722227), Azurion 5 M20 (722228), Azurion 7 B12 (722067, 722225), Azurion 7 B20 (722068, 722226), Azurion 7 M12 (722078, 722223), Azurion 7 M20 (722079, 722224). It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service. Issues with an HDD may, depending on the specific system PC in which the affected HDD is installed, result in loss of imaging functionality. Additionally, in Allura systems, this may lead to loss of motorized movement, or loss of data. In some cases, a system restart may temporarily restore functionality.	FDA Z-2258-2026	Medical Device	High	Jun 3, 2026 Recall: Apr 30, 2026	Details

Showing 2,551 - 2,575 of 4,975 product recalls

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Browse new and recently updated notices across consumer products, foods, vehicles, medical devices and household items.

What To Enter In The Search Box

A recall usually applies to specific products, batches, model ranges or dates. Use the details printed on the item, package, label, receipt or vehicle paperwork.

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.

UPC, Lot Code And Dates

For food, drugs, cosmetics and packaged goods, compare the UPC, lot code, product code, best-by date, use-by date and package size.

Model, Serial Or Date Code

For appliances, electronics, toys, furniture and baby products, match the model number, serial range, date code, color, size and retailer listing.

VIN Or NHTSA Campaign

This site can find vehicle recall campaigns. For your exact car, use the official NHTSA VIN lookup to confirm unrepaired recall status.

Official Sources This Checker Organizes

The goal is to make official notices easier to search. The final decision should still come from the linked agency or manufacturer notice.

CPSC

Consumer Product Recalls

Consumer products, toys, furniture, appliances, electronics and baby products. CPSC remedy details can change after a notice is first posted.

FDA

Food And Medical Device Recalls

FDA-regulated foods, drugs, cosmetics and medical devices. FDA notes that not every recall has a press release on the public recalls page.

USDA FSIS

Meat, Poultry And Egg Product Recalls

Meat, poultry and egg product recalls and public health alerts. Check establishment numbers, lot codes, labels and affected states.

NHTSA

Vehicle, Tire And Car Seat Recalls

Vehicle, tire, equipment and child-seat campaigns. VIN or license plate lookup is needed to know whether your specific vehicle still needs repair.

How To Confirm A Recall Match

1. Search The Obvious Name First

Use the brand, product name, manufacturer or retailer. If the result list is long, add a code from the label or package.

2. Open The Closest Result

Read the product description, recall reason, hazard, affected dates, source agency and official recall number before taking action.

3. Match Every Identifier

Compare the UPC, lot, best-by date, establishment number, model, serial range, color, size, state, retailer and product photo.

4. Follow The Official Remedy

The notice may say stop using, do not eat, discard, return for refund, request a repair kit, replace a part or schedule dealer service.

When A Recall Result Looks Like Your Product

Use this checklist before you throw away a product, call the company, request a refund or schedule a repair.

If It Is Food, Formula Or Pet Food

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.

If It Is A Baby Or Household Product

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.

If It Is A Vehicle Or Car Seat

Use campaign results to understand the issue, then verify your VIN, car seat model or tire information with NHTSA or the manufacturer.

If The Details Do Not Match

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.

What Is A Product Recall?

A product recall is a safety or compliance notice saying a product may need to be corrected, removed, returned, repaired, replaced, refunded or discarded.

What Should You Do After Finding A Recall?

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.

Why Recall Details Must Match Exactly

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.

How To Avoid Fake Recall Notices

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.

Product Recall FAQ

Short answers for common product recall searches.

Can I search product recalls by UPC code?

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.

Can I search product recalls by lot code?

Yes. Lot codes are especially useful for food, drug, cosmetic and pet food recalls because only certain production batches may be affected.

Does this replace a VIN recall lookup?

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.

Are all recalls listed here?

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.

Product Recall Checker: Search Recalls by UPC, Lot Code, Brand or Model

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