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

Latest Product Recall Matches

Showing 2,701 - 2,725 of 3,321 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Beloems Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails This recall involves Beloems-branded adult portable bed rails, model BL-BR201. The recalled foldable bed rails have white metal tubing with either rounded black or gray foam rubber handle grips, support legs and a fabric pouch. The "Beloems" logo is printed on the bed rail's fabric cover and the model number on the owner's manual.	CPSC 10615	Consumer Product	High	Feb 13, 2026 Recall: Feb 12, 2026	Details
Engine Failure Nissan North America, Inc. (Nissan) is recalling certain 2023-2025 Rogue vehicles equipped with 3-cylinder 1.5L variable compression turbo (VC-Turbo) engines. Increased temperatures can break down the engine oil, which may cause the engine bearings to seize and become damaged, leading to engine failure. Engine failure can cause a loss of drive power, increasing the risk of a crash. A bearing failure may cause a breach in the engine block, allowing hot oil to be discharged, increasing the risk of an engine fire.	NHTSA 26V080000	Vehicle	High	Feb 12, 2026 Recall: Feb 12, 2026	Details
Gears in the Electronic Throttle Body May Break Nissan North America, Inc. (Nissan) is recalling certain 2024-2025 Rogue vehicles equipped with 3-cylinder 1.5L variable compression turbo (VC-Turbo) engines. The gears in the electronic throttle body assembly may break. Broken throttle body gears can cause a loss of drive power, increasing the risk of a crash.	NHTSA 26V081000	Vehicle	High	Feb 12, 2026 Recall: Feb 12, 2026	Details
Rearview Camera May Fail General Motors, LLC (GM) is recalling certain 2024 Lyriq vehicles. The rearview camera screen may turn gray with no camera image. An inoperative rearview camera can reduce the driver's rear visibility, increasing the risk of a crash.	NHTSA 26V082000	Vehicle	High	Feb 12, 2026 Recall: Feb 12, 2026	Details
Rear Wheel Lock Up from Transmission Control Valve Failure General Motors, LLC is recalling certain 2020 Chevrolet Silverado 2500, 3500, GMC Sierra 2500, 3500, and 2020-2022 Chevrolet Silverado 1500 and GMC Sierra 1500 vehicles that may have been repaired incorrectly under recall 24V797. The transmission control valve may fail and cause the rear wheels to lock up. Rear wheel lock up increases the risk of a crash.	NHTSA 26V083000	Vehicle	High	Feb 12, 2026 Recall: Feb 12, 2026	Details
Brakes May Fail to Activate with Adaptive Cruise Control International Motors, LLC (International) is recalling certain 2026-2027 MV vehicles. The ECU software may fail to engage the brakes with adaptive cruise control (ACC) or hill hold assist. A vehicle that does not automatically brake as expected increases the risk of a crash.	NHTSA 26V084000	Vehicle	High	Feb 12, 2026 Recall: Feb 12, 2026	Details
DriBiz Recalls Ammo Tabs Desiccant Tiles Due to Injury Hazard This recall involves Ammo Tabs, rectangular, off-white fiber desiccant tiles measuring about 2 inches by 4 inches with a thickness of 2.5mm. The tiles are used within ammunition cans and pistol cases to absorb and lock in humidity. Model number AMT-010 is printed on the packaging.	CPSC 10609	Consumer Product	Medium	Feb 12, 2026 Recall: Feb 5, 2026	Details
Airova Recalls Aroeve Air Purifiers Due to Fire and Burn Hazards This recall involves Aroeve brand air purifiers, model MK04. The recalled air purifiers come in black or white. The model, date code, and serial number information are printed on the product label located on the bottom of the air purifiers. The air purifiers subject to this recall were manufactured prior to July 2025 and have a serial number starting with "BN".	CPSC 10608	Consumer Product	Unknown	Feb 12, 2026 Recall: Feb 9, 2026	Details
SOOWERY 6-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units This recall involves SOOWERY 6-Drawer Dressers. The dressers were sold in black. They have a metal frame, wooden top, and six collapsable fabric drawers. The dressers are 47.2 inches long by 11.8 inches wide by 33.3 inches tall.	CPSC 10611	Child/Baby	High	Feb 12, 2026 Recall: Feb 12, 2026	Details
LShome Photoelectric Smoke Detector Fire Alarms Recalled Due Failure to Warn During Fire Posing Serious Injury or Death Hazard; Sold Exclusively on Amazon.com by TIANJINSHIHAOWEIXINSHENGJIDIANANZHUANGGONGCHENG This recall involves 3-Pack Smoke Detector Fire Alarms. The alarms are 9V battery operated and have a light sound warning and test button. The alarms are white and circular in shape. Model number "XG-7D04-KZ9Z" and SKU number "CX-50YP-A5VN" are printed on the bottom side of the alarm.	CPSC 10610	Consumer Product	High	Feb 12, 2026 Recall: Feb 12, 2026	Details
Vivoo Vaginal pH Test Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or inaccurate diagnostic result by lay person and lead to inappropriate medical intervention.	FDA Z-1266-2026	Medical Device	High	Feb 11, 2026 Recall: Nov 22, 2025	Details
Vortex Surgical Lindsell Sutured IOL Marker, VS0390 - Scleral Marker There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.	FDA Z-1256-2026	Medical Device	High	Feb 11, 2026 Recall: Dec 16, 2025	Details
Menopause Test Cassette (Urine) Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or inaccurate diagnostic result by lay person and lead to inappropriate medical intervention.	FDA Z-1260-2026	Medical Device	High	Feb 11, 2026 Recall: Nov 22, 2025	Details
Brand Name: Da Vinci Product Name: da Vinci X, Xi Surgical System, & da Vinci 5 Surgical System Model/Catalog Number: IS4000; IS4200; IS5000 Software Version: N/A Product Description: The da Vinci Xi, X, and da Vinci 5 surgical systems each consist of three main components: the Surgeon Console (SC), the Vision Cart (VC), and the Patient Cart (PC). The PC is the operative component of the system, and its primary function is to support the instrument arms and camera arm. Each system have four Universal Surgical Manipulators (USMs) also known as arms, which allow the surgeon to control up to thre Due to a software implementation error that allowed instruments arms failing an important diagnostic test to remain in clinical use. This test was supposed to be used to detect Universal Surgical Manipulator insertion axis ball screws that exhibit the symptoms of being bent and misaligned which is a precursor to potential ball screw fatigue failure/fraction	FDA Z-1232-2026	Medical Device	High	Feb 11, 2026 Recall: Nov 7, 2025	Details
Product Name: Lumipulse G pTau 217 Plasma Immunoreaction Cartridges Model/Catalog Number: 81550 Software Version: Not Applicable Product Description: Lumipulse G pTau 217 Plasma Immunoreaction Cartridges (IRC): Lumipulse G pTau 217 Plasma is an assay system, including a set of immunoassay reagents (Lumipulse G pTau 217 Plasma IRC), for the quantitative measurement of pTau 217 in K2EDTA plasma specimens based on chemiluminescent enzyme immunoassay (CLEIA) technology by a specific two-step immunoassay method on the LUMIPULSE G System. 3 ¿ 14 Tests: 3 racks, 14 IRCs per rack, 1 test per IRC. Each Customers may experience inaccurate test results by observing a higher frequency of classification in the indeterminate and positive zone and/or low specificity when compared back to FDA-cleared CSF ratio/PET imaging, due to falsely elevated positive ratio or falsely elevated indeterminate ratio results causing an incorrect classification of a patient as having amyloid pathology associated with Alzheimer s disease (positive result) and/or requiring more clinical testing of that patient (indeterminate result).	FDA Z-1302-2026	Medical Device	High	Feb 11, 2026 Recall: Dec 11, 2025	Details
Brand Name: Molift Product Name: Molift Mover 300 Model/Catalog Numbers: (1) M1501, (2) M1502, (3) M1504, (4) M15050, (5) M15151, (6) M15001, (7) M15002; Product Description: The mobile hoist is an assistive device intended for alleviation of, or compensation for, a functional, impairment due to an injury or disability. The device is designed for an individual lacking the ability to stand up and transfer themselves to / from a bed, the floor, a wheelchair, a chair, a toilet or similar due to reduced mobility or physical strength. Component: The deformation occurs between the bolt and the fork A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformation of the materials involved between the lifting bar and the arm of the device. Such deformation can lead to limited mobility in the joint, which prevents proper functionality of the equipment.	FDA Z-1309-2026	Medical Device	High	Feb 11, 2026 Recall: Nov 17, 2025	Details
Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC433Q-0720; Software Version: N/A Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current. Devices which did not undergo thermoforming could deform and lose performance.	FDA Z-1283-2026	Medical Device	High	Feb 11, 2026 Recall: Jan 7, 2026	Details
Product Name: Nasal Jejunal Feeding Tube REF: NJFT-10 Nasal feeding tube packaged without the nasal transfer tube component.	FDA Z-1298-2026	Medical Device	High	Feb 11, 2026 Recall: Dec 15, 2025	Details
EMPOWR Acetabular System: Liner, 10 degree Hooded, HXe+, 36H, REF: 942-01-36H; Liner, 10 degree Hooded, HXe+, 36J, REF: 942-01-36J; Liner, 10 degree Hooded, HXe+, 40G, REF: 942-01-40G; Liner, 10 degree Hooded, HXe+, 32C, REF: 942-01-32C 942-01-40G acetabular system package was found to contain 942-01-36H acetabular system; and several other acetabular system and knee insert devices may also have a packaging discrepancy, which may cause surgical delay to exchange devices or revision surgery.	FDA Z-1234-2026	Medical Device	High	Feb 11, 2026 Recall: Jan 5, 2026	Details
Rumex Disposable Diamond Dusted ILM Elevator, 12-7523 There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.	FDA Z-1253-2026	Medical Device	High	Feb 11, 2026 Recall: Dec 16, 2025	Details
NAEOTOM Alpha.Prime Software applications: syngo.CT Brain Quantification syngo.CT Vessel Hyperdensities syngo.CT ASPECTS To remove the software applications from certain CT systems as the applications have not received FDA 510(k) clearance.	FDA Z-1241-2026	Medical Device	High	Feb 11, 2026 Recall: Dec 19, 2025	Details
Brand Name: Molift Product Name: Molift 2-point sling bars (Accessory to mobile hoists) Model/Catalog Numbers: (1) 1530101, (2) 1530102 Product Description: The mobile hoist is an assistive device intended for alleviation of, or compensation for, a functional, impairment due to an injury or disability. The device is designed for an individual lacking the ability to stand up and transfer themselves to / from a bed, the floor, a wheelchair, a chair, a toilet or similar due to reduced mobility or physical strength. A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformation of the materials involved between the lifting bar and the arm of the device. Such deformation can lead to limited mobility in the joint, which prevents proper functionality of the equipment.	FDA Z-1310-2026	Medical Device	High	Feb 11, 2026 Recall: Nov 17, 2025	Details
Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens, Catalog VFD 2. Volk Magnifying Lens, Catalog VMD There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of bioburden contamination which could lead to infection.	FDA Z-1244-2026	Medical Device	High	Feb 11, 2026 Recall: Dec 16, 2025	Details
Bubble Sensor for 3/8" x 3/32" tubing; Model Number: 701055720; Internal investigations have identified an issue with the durability of the connecting cable near the connection to the Venous Bubble Sensor. Excessive bending of the connecting cable can lead to full damage of the Venous Bubble Sensor or loose cable contact, which may trigger the errors Ven. bubble sensor defective or Ven. bubble sensor disconnected on the connected medical device. These errors can occur temporarily when the connecting cable is moved or permanently if the connection is fully compromised.	FDA Z-1300-2026	Medical Device	High	Feb 11, 2026 Recall: Jan 9, 2026	Details
LH One Step Ovulation Test Device (Urine) Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers; devices may cause false or inaccurate diagnostic result by lay person and lead to inappropriate medical intervention.	FDA Z-1259-2026	Medical Device	High	Feb 11, 2026 Recall: Nov 22, 2025	Details

Showing 2,701 - 2,725 of 3,321 product recalls

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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

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Model, Serial Or Date Code

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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

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CPSC

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FDA-regulated foods, drugs, cosmetics and medical devices. FDA notes that not every recall has a press release on the public recalls page.

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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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