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

Latest Product Recall Matches

Showing 2,501 - 2,525 of 4,622 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94965; Cardiopulmonary bypass vascular catheter Certain lots of product have the potential for a sterile barrier breach.	FDA Z-2222-2026	Medical Device	High	May 27, 2026 Recall: Apr 21, 2026	Details
Tangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers: (1) TNG4002-IND. (2) TNG-4007-6pk. Affected devices exhibited fractures at the distal shaft tip without complete detachment.	FDA Z-2209-2026	Medical Device	High	May 27, 2026 Recall: Mar 23, 2026	Details
Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 33424 Silastic Brand Foley Catheter 5cc REF: 33614 33616 33618 33620 33622 33624 Due to stain present on the surface of affected foley catheters.	FDA Z-2226-2026	Medical Device	High	May 27, 2026 Recall: Apr 23, 2026	Details
OneLIF Interbody Cage (REF/Description): 010-107-1007/Small 7 Degree 10mm X 7mm, 010-107-1007-2/Small 7 Degree 10mm X 7mm - Oblique, 010-107-1209/Small 7 Degree 12mm X 9mm, 010-107-1411/Small 7 Degree 14mm X 11mm, 010-107-1613/Small 7 Degree 16mm X 13mm, 010-113-1006/Small, 13 Degree 10mm X 6mm, 010-113-1006-2/Small, 13 Degree, 10mm X 6mm - Oblique, 010-113-1208/Small 13 Degree 12mm X 8mm, 010-113-1410/Small 13 Degree 14mm X 10mm, 010-113-1612/Small 13 Degree 16mm X 12mm, 010-119-1407/19 Degree 14mm X 7mm, 010-119-1609/Small 19 Degree 16mm X 9mm, 010-119-1811/Small 19 Degree 18mm X 11mm, 010-1 Intervertebral body fusion system straight inserter failed to properly attach to affected cages, which may result in an inability to securely engage the implant with the inserter, which could lead to procedural delay and/or the need to select an alternative implant.	FDA Z-2213-2026	Medical Device	High	May 27, 2026 Recall: Apr 23, 2026	Details
Philips Azurion systems not configured with an optional auxiliary pan handle. Includes the below product descriptions and corresponding model numbers. 1. Azurion 3 M12; Model Numbers: 722063, 722229. 2. Azurion 3 M15; Model Numbers: 722222, 722064, 722280, 722230. 3. Azurion 5 M12; Model Numbers: 722227, 722231. 4. Azurion 5 M20; Model Numbers: 722228, 722232, 722281. 5. Azurion 7 B12; Model Numbers: 722067, 722225, 722235. 6. Azurion 7 B20; Model Numbers: 722068, 722226, 722236. 7. Azurion 7 M12; Model Numbers: 722078, 722223, 722233. 8. Azurion 7 M20; Model Numbers: 722079, 722224, 722234, 7 Potential safety issue with Philips Azurion systems, where longitudinal and transverse table movements may be impacted due to mechanical wear of the Float Tabletop control on the control module.	FDA Z-2225-2026	Medical Device	High	May 27, 2026 Recall: Apr 28, 2026	Details
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94915; Cardiopulmonary bypass vascular catheter Certain lots of product have the potential for a sterile barrier breach.	FDA Z-2221-2026	Medical Device	High	May 27, 2026 Recall: Apr 21, 2026	Details
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94665; Cardiopulmonary bypass vascular catheter Certain lots of product have the potential for a sterile barrier breach.	FDA Z-2217-2026	Medical Device	High	May 27, 2026 Recall: Apr 21, 2026	Details
Swan-Ganz Pacing Catheter, Models: D200F7; Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.	FDA Z-2204-2026	Medical Device	High	May 27, 2026 Recall: Apr 8, 2026	Details
Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T; Cardiopulmonary bypass vascular catheter Certain lots of product have the potential for a sterile barrier breach.	FDA Z-2214-2026	Medical Device	High	May 27, 2026 Recall: Apr 21, 2026	Details
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94215T; Cardiopulmonary bypass vascular catheter Certain lots of product have the potential for a sterile barrier breach.	FDA Z-2216-2026	Medical Device	High	May 27, 2026 Recall: Apr 21, 2026	Details
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913; Cardiopulmonary bypass vascular catheter Certain lots of product have the potential for a sterile barrier breach.	FDA Z-2219-2026	Medical Device	High	May 27, 2026 Recall: Apr 21, 2026	Details
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94725; Cardiopulmonary bypass vascular catheter Certain lots of product have the potential for a sterile barrier breach.	FDA Z-2218-2026	Medical Device	High	May 27, 2026 Recall: Apr 21, 2026	Details
Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063), Azurion 3 M15 (722064), Azurion 7 B12 (722067), Azurion 7 B20 (722068), Azurion 7 M12 (722078), Azurion 7 M20 (722079, 722224). The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in oil leakage. Oil leakage may affect the cooling performance of the X-ray tube. When the oil flow drops below a certain threshold, the system automatically switches to low-dose fluoroscopy and displays the message Low load fluoroscopy flavor selected: Tube cooler problem . This condition cannot be resolved by restarting the system.	FDA Z-2227-2026	Medical Device	High	May 27, 2026 Recall: Apr 28, 2026	Details
Swan-Ganz Jr Catheter, Models: SGPT54, SGPT64P, SGPT755P Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.	FDA Z-2203-2026	Medical Device	High	May 27, 2026 Recall: Apr 8, 2026	Details
Improperly Tightened Shock Bolts Ember Recreational Vehicles, INC. (Ember) is recalling certain 2026-2027 Touring Edition 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, increasing the risk of a crash.	NHTSA 26V339000	Vehicle	High	May 27, 2026 Recall: May 27, 2026	Details
Instrument Panel Display Failure/FMVSS 101, 305 Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2025 Lexus UX Hybrid, 2024 Lexus GX, Toyota Mirai, and 2024-2025 Toyota Land Cruiser Hybrid vehicles. The instrument panel cluster combination meter may fail to display certain warnings or indicators. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 101, "Control and Displays" and in addition, for the subject Mirai vehicles, FMVSS 305, "Electric-powered vehicles: Electrolyte Spillage and Electrical Shock Protection." An instrument panel display that fails to show critical safety information, such as engine coolant temperature or electrical charge increases the risk of a crash or injury.	NHTSA 26V341000	Vehicle	High	May 27, 2026 Recall: May 27, 2026	Details
Incorrectly Colored Cargo Carrying Capacity Label/FMVSS 120 Tiffin Motorhomes, Inc. (Tiffin) is recalling certain 2026-2027 Open Trail, Wayfarer, and 2026 Midas recreational vehicles. The Cargo Carrying Capacity (CCC) label may have been incorrectly printed on a white label. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 120, "Wheels and Rims-Other Than Passenger Cars." The incorrect label color may make it difficult for the operator to locate the loading or tire pressure information, increasing the risk of a crash.	NHTSA 26V342000	Vehicle	High	May 27, 2026 Recall: May 27, 2026	Details
Loss of Drive Power from Engine Failure Ford Motor Company (Ford) is recalling certain 2025-2026 Explorer, Ranger, and Bronco vehicles. The engine may fail, which can result in a loss of drive power. A sudden loss of drive power can increase the risk of a crash.	NHTSA 26V343000	Vehicle	High	May 27, 2026 Recall: May 27, 2026	Details
Seat Belt May Fail to Retract or Extend Ford Motor Company (Ford) is recalling certain 2018-2022 Expedition and Lincoln Navigator vehicles. The seat belt pretensioner in the driver and/or front passenger seat may inadvertently lock the seat belt, which will not allow the belt to retract or extend. Seat belts that do not retract or extend can fail to restrain an occupant as intended, increasing the risk of injury in a crash.	NHTSA 26V344000	Vehicle	High	May 27, 2026 Recall: May 27, 2026	Details
Incorrect Tire and Weight Capacity Information/FMVSS 110 Ford Motor Company (Ford) is recalling certain 2026 Ranger and Bronco vehicles. The vehicle specifications listed on the tire placard and safety certification labels may be incorrect, including the VIN, capacity weight, seating capacity, front and rear gross axle weight rating (GAWR), tire and rim dimensions, and recommended cold tire pressure. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 110, "Tire Selection and Rims" and 49 CFR Part 567, "Certification." The incorrect tire size, tire pressures, and GAWR listed on the labels can allow the vehicle to be overloaded or have improperly inflated tires, increasing the risk of a crash.	NHTSA 26V335000	Vehicle	High	May 26, 2026 Recall: May 26, 2026	Details
Incorrectly Tightened Shock Bolts Forest River, Inc. (Forest River) is recalling certain 2026 Riverstone, Cedar Creek, and 2024 R-Pod recreational trailers equipped with 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 26V336000	Vehicle	High	May 26, 2026 Recall: May 26, 2026	Details
Incorrectly Tightened Shock Bolts Alliance RV, LLC (Alliance) is recalling certain 2025-2027 Paradigm 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 to other vehicles, increasing the risk of a crash.	NHTSA 26V337000	Vehicle	High	May 26, 2026 Recall: May 26, 2026	Details
Park Outside: Fuel Tank Puncture May Cause Fire Tiffin Motorhomes, Inc. (Tiffin) is recalling certain 2025-2026 GT1, 2026 GH2, and GH1 motorhomes. A screw may have punctured the fuel tank during manufacturing, causing a fuel leak. A fuel leak in the presence of an ignition source, increases the risk of a fire.	NHTSA 26V338000	Vehicle	High	May 26, 2026 Recall: May 26, 2026	Details
PandaEar Recalls Portable Hook-On Chairs Due to Risk of Serious Injury or Death from Fall Hazard; Violates Mandatory Standard for Portable Hook-On Chairs This recall involves two models of PandaEar portable hook-on chairs. The chairs are used to seat young children at the dining table. The chairs contain a black or gray metal frame covered with black, gray, or blue (dinosaur theme) polyester and cotton material and an attached restraint in the occupant seating area. There are two metal arms with plastic covers on top that anchor to a dining table, and the child is suspended from the table. "Panda Ear" can be found on a label stitched to the side of the fabric seats. "Model C2102" can be found on a label located on the bottom of the fabric seats. There are no markings on the product for model BTC-51.	CPSC 10784	Consumer Product	High	May 26, 2026 Recall: May 21, 2026	Details
Orb Funkee Squeeze Toys Recalled Due to Risk of Serious Injury or Death from Asbestos Exposure; Imported by The Orb Factory This recall involves two models of Orb Funkee squeeze toys with the date code 3102491A. The products are made of a soft, stretchable material and filled with sand. Model 17451 is a large golden monkey (stylized "monkee"), and model 41929 is an assortment of small "monkees" in various colors, including orange, purple and green. The date code can be found on the hand of the golden monkee or the back of the smaller monkees.	CPSC 10782	Consumer Product	High	May 26, 2026 Recall: May 21, 2026	Details

Showing 2,501 - 2,525 of 4,622 product recalls

Prev 1 ... 99 100 101 102 103 ... 185 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