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

Latest Product Recall Matches

Showing 1,576 - 1,600 of 3,085 matching product recalls.

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.	CPSC 10735	Child/Baby	High	Apr 24, 2026 Recall: Apr 23, 2026	Details
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	Details
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.	NHTSA 26V261000	Vehicle	High	Apr 23, 2026 Recall: Apr 23, 2026	Details
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.	NHTSA 26V262000	Vehicle	High	Apr 23, 2026 Recall: Apr 23, 2026	Details
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.	NHTSA 26E025000	Vehicle	High	Apr 23, 2026 Recall: Apr 23, 2026	Details
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.	NHTSA 26V263000	Vehicle	High	Apr 23, 2026 Recall: Apr 23, 2026	Details
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.	NHTSA 26V264000	Vehicle	High	Apr 23, 2026 Recall: Apr 23, 2026	Details
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	Details
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.	FDA H-0664-2026	Food	High	Apr 22, 2026 Recall: Mar 20, 2026	Details
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.	FDA H-0665-2026	Food	High	Apr 22, 2026 Recall: Mar 23, 2026	Details
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	Details
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	Medical Device	High	Apr 22, 2026 Recall: Mar 19, 2026	Details
Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015. Increased rate of out-of-specification endotoxin results.	FDA Z-1818-2026	Medical Device	High	Apr 22, 2026 Recall: Mar 19, 2026	Details
Cytal Wound Matrix 2-Layer 7x10 cm. Product ID: WSM0710. Increased rate of out-of-specification endotoxin results.	FDA Z-1817-2026	Medical Device	High	Apr 22, 2026 Recall: Mar 19, 2026	Details
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.	FDA Z-1803-2026	Medical Device	High	Apr 22, 2026 Recall: Mar 19, 2026	Details
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.	FDA Z-1810-2026	Medical Device	High	Apr 22, 2026 Recall: Mar 12, 2026	Details
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	Details
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.	FDA Z-1800-2026	Medical Device	High	Apr 22, 2026 Recall: Mar 19, 2026	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	Details
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
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? or should display but does not appear. 3. After performing Surview and planning the Brain Helical acquisition by setting Brain Area DoseRight Index to increase the dose, there is the potential that the Define Head Area option in the context menu is grayed out.	FDA Z-1825-2026	Medical Device	High	Apr 22, 2026 Recall: Mar 7, 2026	Details
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	Medical Device	High	Apr 22, 2026 Recall: Mar 19, 2026	Details
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

Showing 1,576 - 1,600 of 3,085 product recalls

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Fresh updates

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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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