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

Latest Product Recall Matches

Showing 3,376 - 3,400 of 4,622 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Burlington Medical, Leg Wraps. Potential for attenuation degradation over time, decreasing the lifespan.	FDA Z-1761-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 11, 2026	Details
Paradigm REAL-Time Veo Insulin Pump (MMT-554, MMT-754) All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.	FDA Z-1752-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 13, 2026	Details
ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013; Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.	FDA Z-1664-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 3, 2026	Details
Artoura Breast Tissue Expanders Reference Numbers: TEXP110RH TEXP120RH TEXP120RUH TEXP130RH TEXP135RH TEXP140RH TEXP150RH Textured, High & Ultra High Profile, Integral Injection Dome, 300cc, 375cc, 535cc, 475cc, 500cc, 600cc, 750cc, Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.	FDA Z-1685-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 18, 2026	Details
Burlington Medical, Wrap Aprons. Potential for attenuation degradation over time, decreasing the lifespan.	FDA Z-1757-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 11, 2026	Details
Paradigm REAL-Time Insulin Pump (MMT-522, MMT-722) All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.	FDA Z-1749-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 13, 2026	Details
eTRAX Needle System Starter Kit 18G (for Aurora Trackers), Part Number 667-152 There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.	FDA Z-1734-2026	Medical Device	High	Apr 8, 2026 Recall: Mar 2, 2026	Details
MiniMed 720G Insulin Pump (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1867) All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.	FDA Z-1745-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 13, 2026	Details
Brand Name: da Vinci S, Si Permanent Cautery Hook Instrument Product Name: da Vinci S, Si Permanent Cautery Hook Instrument Model/Catalog Number: 420183 Software Version: NA Product Description: EndoWrist Instruments or da Vinci S/Si Reusable instruments, including blunt and sharp endoscopic dissectors, scissors, scalpels, forceps/pick-ups, needle holders, endoscopic retractors, electrocautery and accessories are intended for endoscopic manipulation of tissue, including grasping, cutting, blunt and sharp dissection, approximation, ligation, electrocautery, suturing, and delivery and placement Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments	FDA Z-1701-2026	Medical Device	High	Apr 8, 2026 Recall: Dec 9, 2025	Details
SIGNA Premier systems Whole-Body MR scanners used to produce images of the inside of the human body to aid diagnosis of disease may have been manufactured/serviced with ferrous (steel) fittings instead of non-ferrous (brass) fittings on the magnet rear and if system is accessed to perform service while the magnet is ramped, the magnetic field could attract the ferrous fittings potentially resulting in personnel injury.	FDA Z-1767-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 27, 2026	Details
THORACIC ROBOTS, DYNJ908777B Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.	FDA Z-1707-2026	Medical Device	High	Apr 8, 2026 Recall: Feb 16, 2026	Details
Incorrect Weight Listed on Label/FMVSS 110 Forest River, Inc. (Forest River) is recalling certain 2026 Westbrook and Avenger travel trailers. The Federal Placard label may list an incorrect dry weight. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 110, “Tire Selection and Rims.” Incorrect weight information may lead to unintentionally overloading the vehicle, increasing the risk of a crash.	NHTSA 26V221000	Vehicle	High	Apr 8, 2026 Recall: Apr 8, 2026	Details
Fuel Pump May Fail Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2015-2022 Lexus RC, 2016-2020 GS, and 2022 IS vehicles. The low-pressure fuel pump inside the fuel tank may fail. Fuel pump failure can cause an engine stall, increasing the risk of a crash.	NHTSA 26V222000	Vehicle	High	Apr 8, 2026 Recall: Apr 8, 2026	Details
Front Brake Failure Bombardier Recreational Products, Inc. (BRP) is recalling certain 2025 Can-Am Origin electric motorcycles. A fatigue failure of the front brake caliper support may occur and result in inoperative front brakes. Front brake failure increases the risk of crash or injury.	NHTSA 26V220000	Vehicle	High	Apr 7, 2026 Recall: Apr 7, 2026	Details
Seat Belt Anchors May Detach Hyundai Motor America (Hyundai) is recalling certain 2023-2025 Hyundai Ioniq 6, 2023-2026 Genesis G90, 2024-2026 Hyundai Santa Fe, and Hyundai Santa Fe Hybrid vehicles. The driver and passenger seat belt anchors may detach. A detached seat belt anchor will not adequately restrain the seat occupant, increasing the risk of injury in a crash.	NHTSA 26V218000	Vehicle	High	Apr 6, 2026 Recall: Apr 6, 2026	Details
Warning Label Missing from Cross View Mirror/FMVSS 111 Greenpower Motor Company Inc. (Greenpower) is recalling certain 2020-2024 Nano Beast and 2021-2024 Beast school buses. The Cross View Mirror is designed to only view pedestrian around stopped buses. The label warning drivers not to use the mirror to view vehicular traffic may be missing. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 111, "Rear Visibility." Without a warning label, the driver may use the altered view to see other vehicles, increasing the risk of a crash.	NHTSA 26V219000	Vehicle	High	Apr 6, 2026 Recall: Apr 6, 2026	Details
Child Seat May Detach from Base/FMVSS 213 Graco Children's Products Inc. (Graco) is recalling certain SnugRide Turn & Slide and Modes Nest Travel Systems with Snugride Turn & Slide infant child seats. Please refer to Graco's recall report for specific model information. The infant seat carrier may detach from the base in a crash. As such, these child seats and travel systems fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 213, "Child Restraint Systems." An infant seat carrier that detaches in a crash increases the risk of injury.	NHTSA 26C003000	Vehicle	High	Apr 3, 2026 Recall: Apr 3, 2026	Details
Drive Shaft Universal Joint May Break Mercedes-Benz USA, LLC (MBUSA) is recalling certain 2018 E 400 4MATIC Sedan, E 400 4MATIC Wagon, E 400 4MATIC Cabriolet, E 400 4MATIC Coupe, 2018-2020 Maybach S 560 4MATIC, S 560 4MATIC Coupe, S 450 4MATIC, 2019-2020 E 450 4MATIC Sedan, E 450 4MATIC Wagon, E 450 4MATIC Coupe, and E 450 4MATIC Cabriolet vehicles. The drive shaft universal joint may break, resulting in a sudden loss of drive power. A sudden loss of drive power increases the risk of a crash.	NHTSA 26V216000	Vehicle	High	Apr 3, 2026 Recall: Apr 3, 2026	Details
Winter Front Cover Interference with Forward Collision Warning System Autocar, LLC (Autocar) is recalling certain 2025-2026 ACX (Xpeditor) vehicles. The winter front cover may interfere with the forward collision warning (FCW) system. Interference may cause the FCW system to fail, increasing the risk of a crash.	NHTSA 26V215000	Vehicle	High	Apr 3, 2026 Recall: Apr 3, 2026	Details
Tuymec Minoxidil Hair Growth Spray Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by DrHealBeauty This recall involves Tuymec Minoxidil Hair Growth Kit. The kits contain two black spray bottles with labels that read "Tuymec Minoxidil Hair Hair Growth", "Advanced Formula" and "5% Minoxidil with BIOTIN". The kits come in black cartons with white and silver lettering that include "Drug Facts" on the back, distributor information on one of its sides, three icons making product claims on its other side, and batch, manufacture and expiration dates on its bottom.	CPSC 10691	Child/Baby	High	Apr 3, 2026 Recall: Apr 2, 2026	Details
TecFlox Hair and Beard Growth Serum Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging This recall involves TecFlox's topical solution bottles. The hair and beard growth serum comes in white plastic bottles fitted with a white nozzle and was sold in packs of four bottles. "TecFlox Minoxidil Topical Solution" is printed on the bottle's label and the manufacture date "MFD 2025.8.25" on the underside of the bottle.	CPSC 10686	Child/Baby	High	Apr 3, 2026 Recall: Apr 2, 2026	Details
Sangohe Reannounces and Expands Adult Portable Bed Rails Recall Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails This recall involves Sangohe-branded adult portable bed rails models 504E and 504Q. Model 504E bed rail comes in black, measures 23 inches wide by 35 inches tall, and weighs nine pounds. The model number "504E" can be found on the outer packaging box, on the product label/sticker attached to the bed rail, and on the first page of the instruction manual. Model 504Q bed rail comes in black, measures 28.5 inches wide by 43.3 inches tall, and weighs nine pounds. The model number "504Q" can be found on the outer packaging box, on the product label/sticker attached to the bed rail, and on the first page of the instruction manual.	CPSC 10688	Consumer Product	High	Apr 3, 2026 Recall: Apr 2, 2026	Details
OCUN NA Recalls Condor HMS Triple Carabiners Due to Risk of Serious Injury or Death from Fall Hazard This recall involves Ocun Condor HMS Triple Carabiners sold in dark gray and blue. The carabiners have an independent internal wire gate for belaying and rappelling and a triple locking action gate. The affected carabiners have the following batch numbers 24003xx, 24004xx, 24010xx, 24023xx, 24024xx, 24025xx, 25005xx, 25006xx. The batch number is found on the spine of the carabiner.	CPSC 10684	Consumer Product	High	Apr 3, 2026 Recall: Apr 2, 2026	Details
HTRC and Haisito T400 Battery Chargers Recalled Due to Risk of Serious Injury and Death from Fire Hazard; Manufactured by Huizhou Haitan Technology This recall involves battery chargers, model T400, sold under the brand names "HTRC" and "Haisito." The recalled chargers are black with a touch screen, and the model number T400 is printed on the front. Some units have the brand name "HTRC" printed on the front, while other units do not have a visible brand name. Units without a visible brand name may still have the model number "T400" printed on the front. The brand name "Haisito" may not be printed on the product but may be located on the purchase receipt.	CPSC 10689	Electronics	High	Apr 3, 2026 Recall: Apr 2, 2026	Details
Gavoyeat Halloween Light-Up Rings Recalled Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Toys; Sold on Amazon by CSZWEICD This recall involves Gavoyeat Halloween Light-Up Rings Party Favors, model number 43398-68657. "B07GF8VD7N" appears on the back of packaging. The light-up rings come with 50 multi-colored party favors that light up and each includes three preinstalled button cell batteries. The batteries are visible through the inner clear casing. The light-up rings have "Holiday Party Favors LED Light Up Ring" printed on the back of the package.	CPSC 10682	Child/Baby	High	Apr 3, 2026 Recall: Apr 2, 2026	Details

Showing 3,376 - 3,400 of 4,622 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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