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

Latest Product Recall Matches

Showing 2,876 - 2,900 of 3,083 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Body Panel Joint Incorrectly Attached/FMVSS 221 Forest River Bus, LLC (Forest River Bus) is recalling certain 2026 Collin Bus transit buses. The body panel joint adhesive may have been applied to the incorrect location, causing the panels to separate. As such these vehicle fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) No. 221, "School Bus Body Joint Strength." Separated body panels can reduce structural integrity, increasing the risk of injury in a crash.	NHTSA 26V040000	Vehicle	High	Jan 23, 2026 Recall: Jan 23, 2026	Details
Body Panel Joint Incorrectly Attached/FMVSS 221 Forest River Bus, LLC (Forest River Bus) is recalling certain 2026 Collins Bus school buses. The body panel joint adhesive may have been applied to the incorrect location, causing the panels to separate. As such these vehicle fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) No. 221, "School Bus Body Joint Strength." Separated body panels can reduce structural integrity, increasing the risk of injury in a crash.	NHTSA 26V041000	Vehicle	High	Jan 23, 2026 Recall: Jan 23, 2026	Details
Solar Panel May Detach From RV Grand Design RV, LLC (Grand Design) is recalling certain 2025-2026 Lineage recreational vehicles. The adhesive securing the solar panels to the roof may fail, allowing the solar panel to detach. A detached solar panel can become a road hazard for other vehicles, increasing the risk of a crash.	NHTSA 26V042000	Vehicle	High	Jan 23, 2026 Recall: Jan 23, 2026	Details
Damaged Parking Brake Wiring Harness General Motors, LLC (GM) is recalling certain 2024-2025 Chevrolet Blazer EV vehicles that may have been repaired incorrectly under recall 25V433. The rear parking brake wiring harness may become damaged or corroded, resulting in unintended activation of the parking brake or loss of the parking brake function. Unintended activation of the parking brake while driving increases the risk of a crash. Loss of the parking brake function while parked can result in a rollaway, increasing the risk of a crash.	NHTSA 26V031000	Vehicle	High	Jan 22, 2026 Recall: Jan 22, 2026	Details
Yetonamr Pull String Teething Toys Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by Longyanguiheng This recall involves the Yetonamr Pull String Teething Toy. The teething toy is an off-white disc shape with either a red ball or blue ball in the middle and six long, silicone pull string "tentacles" of various colors running through the ball. There are also three free-spinning rings and soft push buttons on the disc. "Model no. 688-59" is printed on the product packaging.	CPSC 10570	Consumer Product	High	Jan 22, 2026 Recall: Jan 22, 2026	Details
Vndueey Magnetic Men Toy Sets Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys This recall involves Vndueey Magnetic Men toy sets. The toy sets consist of 10 flexible, stick figures in red, orange, pink, yellow, blue, bright red, bright green and transparent. Each stick figure has four small magnets, one in each hand and foot.	CPSC 10574	Child/Baby	High	Jan 22, 2026 Recall: Jan 22, 2026	Details
Topkay Lighters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violates Mandatory Standard for Multipurpose Lighters; Sold on Amazon by Xiyude This recall involves Topkay Torch Lighters. The metal lighters are black and come in a two-pack. "Honest" is printed on the front of lighter.	CPSC 10572	Child/Baby	High	Jan 22, 2026 Recall: Jan 22, 2026	Details
Mikario Trading Convertible Baby Gyms Recalled Due to Risk of Serious Injury or Death from Suffocation; Violate Mandatory Standard for Infant Support Cushions; Sold on TikTok Shop This recall involves Mikario Trading's 5-in-1 baby gyms. The recalled baby gyms convert from an activity center to a tummy-time pillow mat. They were sold in pink and have a toy bar, six detachable plush toys and a set of milestone cards. "Baby Gym" and "Item No.: CBPBG-PIN" are printed on a label stitched to the product on the edge of the mat at the bottom.	CPSC 10577	Child/Baby	High	Jan 22, 2026 Recall: Jan 22, 2026	Details
Iristar Minoxidil Spray Bottles for Hair and Beard Growth Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by Moralowen This recall involves Iristar Minoxidil Spray Bottles, 5% minoxidil with biotin for hair and beard growth. The sprays come in black plastic bottles with navy blue labels and white highlights with a spray cap. The bottles and outer packaging are labeled "Iristar" and "Minoxidil Spray" on the front and ingredients and directions for use are found on the back.	CPSC 10576	Child/Baby	High	Jan 22, 2026 Recall: Jan 22, 2026	Details
Gagaku Children's Ice Cream Toy Playsets Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion Hazard; Violate Mandatory Standard for Toys; Sold on Amazon by Brandworl.USA This recall involves Gagaku-branded ice cream shop toy playsets. The recalled toy set includes 16 wooden pieces: a cash register, three ice cream cones, six scoops of ice cream, four popsicles, and two cupcakes in varying colors or "flavors." It also comes with one plastic credit card, five plastic dollar bills, one plastic menu and a two-level pink display box labeled "ICE-CREAM" on the front, with a black sign on the side. "GAGAKU" and "Model: KABI-0176 G062401IC" are printed on a label on the underside of the toy.	CPSC 10571	Child/Baby	High	Jan 22, 2026 Recall: Jan 22, 2026	Details
Based Online Fidget Magnet Ball Toys Recalled Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys This recall involves Based Online Fidget Magnet Ball Toy Sets. Each set includes four textured, silicone-covered magnet balls in white, yellow, blue and purple. Each ball is about 1.24 inches in diameter. The magnet toys come in a black fabric zippered case. There are no identifying marks on the magnet toys.	CPSC 10573	Child/Baby	High	Jan 22, 2026 Recall: Jan 22, 2026	Details
Aborder Products Recalls Cumbor Retractable Safety Gates Due to Risk of Serious Injury or Death to Children from Entrapment; Violates Mandatory Standard for Gates and Enclosures This recall involves Cumbor-branded retractable safety gates. The recalled gates have a metal frame and a mesh screen that measures about 34 inches high with an adjustable width up to 55 inches. The gates were sold in black, gray, and white and came with one or more suction cups. "Model Name: Retractable Safety Gate," "Model Number: S5V2" and "Cohort Information: A202504S5V2A001" are printed on a label sewn to the mesh screen.	CPSC 10575	Child/Baby	High	Jan 22, 2026 Recall: Jan 22, 2026	Details
Medline medical procedure convenience kits labeled as: 1) ROBOTIC, REF CDS980523M; 2) ROBOTIC GYN, REF CDS980647K; 3) DAVINCI PROCEDURE, REF CDS980864Q; 4) GYN-URO LAPSCP CDS-LF, REF CDS981583U; 5) GYN-URO LAPSCP CDS-LF, REF CDS981583V; 6) GYN ROBOTIC, REF CDS981826K; 7) DEPAUL DAVINCI CDS, REF CDS982377K; 8) GU DAVINCI, REF CDS982779N; 9) GYN DAVINCI, REF CDS982780V; 10) UNIVERSAL ROBOTIC ORLANDO, REF CDS982857K; 11) ROBOTIC GU/GYN, REF CDS983393L; 12) GYN LAPAROSCOPY CDS, REF CDS984656Q; 13) GYN LAPAROSCOPY CDS, REF CDS984656R; 14) DAVINCI CDS UCC-LF, REF CDS984663J; 15) ROBOTIC UROLOGY PROS Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and battery pack during use of the Strykeflow 2 Suction Irrigator. This design change has caused some devices to leak and/or emit vaporized saline (which can resemble smoke) during use.	FDA Z-1088-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 16, 2025	Details
Allura Xper FD20; Model Number: 722006; Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.	FDA Z-1066-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 15, 2025	Details
Allura Xper FD10; Model Number: 722026; Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.	FDA Z-1073-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 15, 2025	Details
FreeStyle Libre 3 Plus Sensor REF 72080-01 UDI-DI code: 00357599819002 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System. Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results	FDA Z-1023-2026	Medical Device	High	Jan 21, 2026 Recall: Nov 24, 2025	Details
Brand Name: PALACOS Product Name: PALACOS MV+G pro 40; PALACOS MV+G pro 80 Model/Catalog Number: 5081290; 5081291 Software Version: N/A Product Description: Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix). Component: N/A increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule breakage. An unfortunate combination of these influence factors can lead to unbreakable ampoules. If none or not all ampoules break, the product cannot be used on the patient since no or no appropriate cement dough is formed.	FDA Z-1082-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 9, 2025	Details
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) OPEN HEART ACCESSORY CDSKit SKU CDS984289O; 2) OPEN HEART CDSKit SKU CDS984355K; 3) BAG A OPEN HEART KITKit SKU DYKM1025D; 4) RR-CABG SUPPLEMENTAL PACKKit SKU DYNJ0394752O; 5) OPEN HEART CDSKit SKU DYNJ902879T; 6) BASIC CARDIAC ANESTHESIAKit SKU DYNJ903523F; 7) OPEN HEART CDSKit SKU DYNJ905557B; 8) AN03 HEART/ANESTHESIA KIT-LFKit SKU PHS972012D. Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.	FDA Z-1050-2026	Medical Device	High	Jan 21, 2026 Recall: Nov 26, 2025	Details
FreeStyle Libre 3 Plus Sensor REF 78769-01 UDI-DI code: 00357599843014 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System. Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results	FDA Z-1022-2026	Medical Device	High	Jan 21, 2026 Recall: Nov 24, 2025	Details
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) RR-LE FORT MANDIBLE PACK-LF, Medline Kit SKU DYNJ0785864R; 2) RR-ASC EAR PACK-LF, Medline Kit SKU DYNJ0792607R. Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.	FDA Z-1052-2026	Medical Device	High	Jan 21, 2026 Recall: Nov 26, 2025	Details
MAXXUS, System, Tomography, Computed, Emission GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and listed in the Affected Product Details section of this letter) could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury. There have been no reports of detector falls or injuries as a result of this potential issue. The Impacted Systems affected by this notice are those that have not been manufactured for several years. GE HealthCare has previously communicated End of Guaranteed Service for these Impacted Systems.	FDA Z-1047-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 10, 2025	Details
Brand Name: PALACOS Product Name: PALACOS R pro 40; PALACOS R pro 80 Model/Catalog Number: 5081286; 5081287 Software Version: N/A Product Description: Radiopaque, poly(methyl methacrylate)-based (PMMA) bone cement, pre-filled into a mixing and application system, suitable for use with or without vacuum (ready to mix). Component: N/A increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule breakage. An unfortunate combination of these influence factors can lead to unbreakable ampoules. If none or not all ampoules break, the product cannot be used on the patient since no or no appropriate cement dough is formed.	FDA Z-1080-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 9, 2025	Details
Brand Name: Catalyst+ Product Name: Catalyst, Catalyst+ Model/Catalog Number: SP001-0026, SP003-0002 Software Version: cSRS module in combination with cMotion module Product Description: GMDN: 40893 Patient positioning device, diagnostic imaging/radiotherapy, laser Component: Not applicable Due to issues with the system's stereotactic radiosurgery (SRS) treatment cannot be guaranteed for all couch angles and system setups. n certain cases, the system may indicate the patient as correctly positioned at the isocenter, even when the isocenter is positioned outside of the indicated tolerance.	FDA Z-1092-2026	Medical Device	High	Jan 21, 2026 Recall: Oct 9, 2025	Details
Allura Xper FD20 Biplane; Model Number: 722013; Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.	FDA Z-1071-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 15, 2025	Details
Allura Xper FD20 OR Table; Model Number: 722023; Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.	FDA Z-1072-2026	Medical Device	High	Jan 21, 2026 Recall: Dec 15, 2025	Details

Showing 2,876 - 2,900 of 3,083 product recalls

Prev 1 ... 114 115 116 117 118 ... 124 Next

Food safety

Food Product Recall Search

Use brand, product name, UPC, lot code, best-by date, package size, allergen, contamination issue or distribution state.

Cars & equipment

Vehicle Recall Lookup

Search campaigns by make, model, year, component or NHTSA number. Use NHTSA's VIN search for vehicle-specific open recall status.

Family safety

Baby Product Recall Alerts

Check cribs, loungers, strollers, toys, formula, baby food and child car seats by brand, model, date code or hazard.

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

Check The Item You Have