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

Latest Product Recall Matches

Showing 2,351 - 2,375 of 4,622 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Philips Azurion 3M12, Model Numbers: 722063, 722221 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.	FDA Z-2284-2026	Medical Device	High	Jun 10, 2026 Recall: Dec 7, 2023	Details
Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the Medrad¿ Avanta Injection System; Catalog number: AVA 500 MPAT (Part 2 of 2); Affected material numbers: 87629007, 60729458, 86566648; Supplier changes resulted in a fit issue with the Contrast Flow Control Valve (CFCV) interface on the Avanta Injector System. Multiple customer reports indicate that the stopcock cannot be reliably engaged with the CFCV snap interface. In instances where engagement is achieved through applied force, the connection is unstable, and the stopcock may disengage before or during contrast injection, leading to procedure interruption.	FDA Z-2296-2026	Medical Device	High	Jun 10, 2026 Recall: Apr 24, 2026	Details
BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet Fingerprint scanner may overheat to a temperature to cause 1st degree burn.	FDA Z-2303-2026	Medical Device	High	Jun 10, 2026 Recall: Apr 30, 2026	Details
BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405632. This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.	FDA Z-2250-2026	Medical Device	High	Jun 10, 2026 Recall: Apr 27, 2026	Details
Brand Name: B. BRAUN MEDICAL INC Product Name: CESK NORTHSIDE ANESTHESIA TRAY Model/Catalog Number: 555076 Software Version: N/A Product Description: CESK NORTHSIDE ANESTHESIA TRAY Component: No B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.	FDA Z-2263-2026	Medical Device	High	Jun 10, 2026 Recall: Jan 29, 2026	Details
Atlan A350XL. Model Number: 8621600. anesthesia workstation The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.	FDA Z-2208-2026	Medical Device	High	Jun 10, 2026 Recall: May 7, 2026	Details
Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050 Temperature probe devices lack FDA clearance.	FDA Z-2273-2026	Medical Device	High	Jun 10, 2026 Recall: Apr 23, 2026	Details
Spinocan Spinal Needle procedure kits: Material Description (Material Number): Spinocan 26 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333201); Spinocan 25 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333211); Spinocan 22 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333231) These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huon Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a recent FDA manufacturing facility inspection.	FDA Z-2277-2026	Medical Device	High	Jun 10, 2026 Recall: May 6, 2026	Details
BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405645. This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.	FDA Z-2251-2026	Medical Device	High	Jun 10, 2026 Recall: Apr 27, 2026	Details
Philips Azurion 3M15, Model Numbers: 722064, 722222 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.	FDA Z-2285-2026	Medical Device	High	Jun 10, 2026 Recall: Dec 7, 2023	Details
Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK HARRIS METHODIST Model/Catalog Number: 555498 Software Version: N/A Product Description: CESK HARRIS METHODIST Component: No B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.	FDA Z-2266-2026	Medical Device	High	Jun 10, 2026 Recall: Jan 29, 2026	Details
Missing Pedestrian Warning Sounds/FMVSS 141 Denago EV is recalling certain 2024-2025 Nomad, 2024-2026 Nomad XL, 2026 Scout 2, 2026 Scout 4, 2024-2026 Rover XL, 2024-2026 Rover XXL, and 2024-2026 Rover XL6 vehicles. The vehicles may fail to make pedestrian warning sounds when in motion. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 141, "Minimum Sound Requirements for Hybrid and Electric Vehicles." A vehicle that does not emit sound may fail to alert pedestrians of a moving vehicle, increasing the risk of a crash or injury.	NHTSA 26V381000	Vehicle	High	Jun 10, 2026 Recall: Jun 10, 2026	Details
Engine Stall From Canister Purge Valve Malfunction Ford Motor Company (Ford) is recalling certain 2012-2018 Focus vehicles previously repaired incorrectly under recall number 18V735. The Canister Purge Valve (CPV) may malfunction, causing the engine to stall unexpectedly while driving. An engine that stalls while driving increases the risk of a crash.	NHTSA 26V369000	Vehicle	High	Jun 9, 2026 Recall: Jun 9, 2026	Details
Instrument Cluster Failure/FMVSS 102 Ford Motor Company (Ford) is recalling certain 2017 F-150 vehicles previously repaired incorrectly under recall number 17V053. The instrument cluster may lose power after initial vehicle start-up in cold ambient temperatures. Several gauges, including the transmission gear position indicator, may not illuminate. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 102, "Transmission Shift Lever Sequence, Starter Interlock, and Transmission Braking Effect." An instrument cluster that fails to display critical safety information, such as gear position or warning lights, increases the risk of a crash or injury.	NHTSA 26V370000	Vehicle	High	Jun 9, 2026 Recall: Jun 9, 2026	Details
Vehicle Rollaway Risk Ford Motor Company (Ford) is recalling certain 2024 Explorer vehicles equipped with a 2.3L engine and 10R60 automatic transmission. An unintentional powertrain control module (PCM) reset may occur while the vehicle is in motion and result in park system damage. A park system that is damaged may not shift into "PARK," resulting in a vehicle rollaway and increasing the risk of injury or crash.	NHTSA 26V371000	Vehicle	High	Jun 9, 2026 Recall: Jun 9, 2026	Details
Instrument Cluster May Go Blank on Start-Up/FMVSS 101 Ford Motor Company (Ford) is recalling certain 2019 Ford Mustang, Lincoln Nautilus, and Lincoln Navigator vehicles previously repaired incorrectly under recall number 19V076. At vehicle start-up, the Instrument Panel Cluster Assembly (IPC) may not function, showing a blank display. As a result, these vehicles fail to comply with Federal Motor Vehicle Safety Standard (FMVSS) number 101, "Controls and Displays." A blank instrument cluster that fails to display critical safety information, such as vehicle speed or safety system warnings, increases the risk of a crash.	NHTSA 26V372000	Vehicle	High	Jun 9, 2026 Recall: Jun 9, 2026	Details
Daytime Running Lights May Not Dim/FMVSS 108 Ford Motor Company (Ford) is recalling certain 2018-2020 F-150 vehicles previously repaired incorrectly under recall number 20V097. When the headlight switch is turned from "Autolamps" to "Headlamps On," the Daytime Running Lamps (DRLs) may remain fully bright instead of dimming to parking lamps as intended. 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." Daytime Running Lamps that do not dim may reduce the visibility of other drivers, increasing the risk of a crash.	NHTSA 26V373000	Vehicle	High	Jun 9, 2026 Recall: Jun 9, 2026	Details
Unintended Vehicle Movement Ford Motor Company (Ford) is recalling certain 2018 F-150 vehicles previously repaired incorrectly under recall number 17V669. Quickly moving the shift lever from Park to Drive may cause a loss of gear indication on the instrument cluster display and a momentary selection of an unintended gear, such as Reverse or Neutral. Unintended gear selection may cause the vehicle to move in an unexpected direction, increasing the risk of crash or injury.	NHTSA 26V375000	Vehicle	High	Jun 9, 2026 Recall: Jun 9, 2026	Details
Steering Wheel Hands-Off Detection Alerts May Fail Ford Motor Company (Ford) is recalling certain 2019 Lincoln Nautilus vehicles previously repaired incorrectly under recall number 19V031. The lane center assist system may not adequately detect if a driver has their hands off the steering wheel for a prolonged period of time. Failure to alert the driver with the intended hands-off the wheel warnings may increase the risk of a crash.	NHTSA 26V377000	Vehicle	High	Jun 9, 2026 Recall: Jun 9, 2026	Details
Hydraulic Jack May Extend Unexpectedly Vermeer Manufacturing Company (Vermeer) is recalling certain 2002-2026 BC1800XL brush chipper trailers. The hydraulic jack may extend unexpectedly. An extended jack may contact the ground while driving, causing a loss of vehicle control and increasing the risk of injury or a crash.	NHTSA 26V379000	Vehicle	High	Jun 9, 2026 Recall: Jun 9, 2026	Details
Unexpected Downshift Can Cause Loss of Control Ford Motor Company (Ford) is recalling certain model year 2014 F-150 vehicles previously repaired incorrectly under recall number 24V444. A loss of signal between the transmission output shaft speed sensor and the powertrain control module (PCM) can cause the transmission to unexpectedly downshift into first gear. Unexpectedly downshifting into first gear may result in a loss of vehicle control, increasing the risk of a crash.	NHTSA 26V378000	Vehicle	High	Jun 9, 2026 Recall: Jun 9, 2026	Details
SUNS International Recalls Residential Elevator Interlock Switches Due to Fall and Crushing Hazard; Risk of Death or Serious Injury This recall involves all SUNS International SS6291 Solenoid Interlock switches used in residential elevators produced from August 20, 2024, through November 6, 2025, with date codes 2431 through 2543. The SUNS SS6291 interlock switch measures approximately 10 inches by 2 inches and weighs about 2-pounds. "SUNS", the model number and date code are printed on a label on the side of the product.	CPSC 10804	Consumer Product	High	Jun 5, 2026 Recall: Jun 4, 2026	Details
Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Broqixin This recall involves Broqixin-branded pool drain covers. The white plastic pool drain covers measure about 7.36 inches in diameter and weigh about 3.84 ounces and come with two screws. "Model 11064W" is printed on the product's packaging.	CPSC 10802	Consumer Product	High	Jun 5, 2026 Recall: Jun 4, 2026	Details
Little Grape Land Recalls Nursing Pillows Due to Risk of Serious Injury or Death from Suffocation; Violate Mandatory Standards for Nursing Pillows and Infant Support Cushions This recall involves Little Grape Land Nursing Pillows. The nursing pillows are U-shaped and come in a rose floral, alligator, bear, butterfly, cactus, construction truck, forest deer, green leaves, little bunny, spring flower and woodland animal patterns. There are no markings or labels on the product.	CPSC 10798	Child/Baby	High	Jun 5, 2026 Recall: Jun 4, 2026	Details
Crenlux Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Eicong This recall involves Crenlux-branded pool drain covers. The white plastic pool drain covers measure about eight inches in diameter and weigh about 12.7 ounces. "Crenlux" is printed on the product's packaging.	CPSC 10800	Consumer Product	High	Jun 5, 2026 Recall: Jun 4, 2026	Details

Showing 2,351 - 2,375 of 4,622 product recalls

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Food safety

Food Product Recall Search

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Vehicle Recall Lookup

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Family safety

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Fresh updates

Latest Product Recalls Today

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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