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

Latest Product Recall Matches

Showing 4,651 - 4,675 of 4,975 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
LuxJet Submersible LED Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries This recall involves LuxJet Submersible LED Lights. The LED lights were sold in sets of 10 LED color changing lights, two remote controls, 20 preinstalled CR2450 lithium batteries in the lights and four preinstalled CR2032 lithium batteries in the remote controls. Each light is about 3.5 cm in diameter.	CPSC 10582	Child/Baby	High	Jan 29, 2026 Recall: Jan 29, 2026	Details
Hobby Lobby Recalls Giraffe and Llama Plush Toys with Clips Due to Drowning Hazard; Manufactured by Starmatrix Group Drowning Hazard; Manufactured by Starmatrix Group This recall involves all Sunneday and Blue Bay brand above-ground pools 48 inches and taller. Model information and the Sunneday or Blue Bay logo are printed on the liner on the outside of the pool. Pool models subject to this recall include: Model Description UPC Code 70018 Sunneday Oasis Cottage 18'x52" 850022858529 70024 Sunneday Oasis Cottage 24'x52" 850022858536 358015W Blue Bay Softsided Pool 15'x48" 191127003583 359015G Blue Bay Softsided Pool 15'x48" 191127003590 360018W Blue Bay Softsided Pool 18'x52" 191127003606 361018G Blue Bay Softsided Pool 18'x52" 191127003613 380018T Blue Bay Softsided Pool 18'x52" 191127003804 The recalled above-ground pools contain a compression strap (also referred to as a reinforcing belt) that wraps around the pool on the outside of the vertical support poles, and may create a foothold, allowing a child to access the pool and drown. Children can still gain access to the pools using these footholds even if the ladder is removed. CPSC's website www.PoolSafely.gov has free, downloadable educational materials available to the public on pool safety including information on barriers, covers, alarms and other safety information.	CPSC 10585	Child/Baby	Unknown	Jan 29, 2026 Recall: Jan 29, 2026	Details
Hobby Lobby Recalls Giraffe and Llama Plush Toys with Clips Due to Choking Hazard This recall involves a Giraffe Plush Toy with clip and a Llama Plush Toy with clip. The Giraffe with clip has a yellow body with a yellow claw clip. The legs of the giraffe are orange and blue with various colored paws. The ears are black and white animal print. The Giraffe measures about nine inches long. The Giraffe has "HL699436 or HL731481" printed on the white sewn-in label. The hang tag on the Giraffe has "2553675" printed on the front left corner. The Llama with clip has a white body with a green claw clip. The body has a mirror and orange triangle teether attached to the body. The legs of the Llama are orange and yellow with various colored paws. The Llama measures about 12 inches long. "HL699436" is printed on the white sewn-in label attached to the body. The hang tag on the plush has "2553634" printed on the front left corner.	CPSC 10584	Child/Baby	Unknown	Jan 29, 2026 Recall: Jan 29, 2026	Details
Gazelle USA Recalls Urban Arrow FamilyNext Pro Cargo E-Bikes Due to Injury Hazard This recall involves Urban Arrow FamilyNext Pro Cargo E-Bikes with Fidlock buckles. The recalled bicycle comes in one size and comes in green and black. The frame of the bicycle is made of aluminum with a reinforced foam (EPP) cargo box. The bicycle is 105" in length and 28" wide. "Urban Arrow" is imprinted on the bottom of the cargo box.	CPSC 10589	Child/Baby	Medium	Jan 29, 2026 Recall: Jan 29, 2026	Details
Bazic Products Recalls Bazic Silicone Glue Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child Resistant Packaging and FHSA Labeling Requirements This recall involves Bazic Silicone Glue, Model 2030. The glue comes in a transparent plastic bottle with a blue nozzle top and a blue and black wraparound label bearing instructions and warning statements. The glue's label reads "Bazic", "Silicone Glue", and "Clear Adhesive Sealant" on the front, with cautionary statements and "2030" above the barcode on its side. Only Bazic Silicone Glue with batch code "V01233-031725-70004523" printed on the side of the bottles are included in the recall.	CPSC 10588	Child/Baby	High	Jan 29, 2026 Recall: Jan 29, 2026	Details
AiTuiTui Pull String Teething Toys Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by Vanfun This recall involves the AiTuiTui 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 pull string "tentacles" of various colors running through the ball. There are also three free-spinning rings on one side and soft push buttons on the disc. "Model: 688-59" is printed on the product packaging.	CPSC 10579	Child/Baby	High	Jan 29, 2026 Recall: Jan 29, 2026	Details
SQ40S Blood Transfusion Filter Due to products being released for distribution prior to completion of the required quality control release process the sterility assurance cannot be confirmed.	FDA Z-1157-2026	Medical Device	High	Jan 28, 2026 Recall: Nov 3, 2025	Details
Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM20 Product Description: The iM20 Patient Monitor System (hereinafter called iM20) can perform long-time continuous monitoring of multiple physiological parameters, including ECG, respiration (RESP), non-invasive blood pressure (NIBP), oxygen saturation of the blood (SpO2), pulse rate (PR), temperature (TEMP), invasive pressure (IBP), Carbon Dioxide (CO2). The system capabilities include storing, displaying, analyzing and controlling such data afterwards. When necessary, alarms will be produced so that doctors and nurses can As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.	FDA Z-1147-2026	Medical Device	High	Jan 28, 2026 Recall: Oct 24, 2025	Details
MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed, REF MDR107002E; 2) Semi Electric Basic Homecare Bed, 4-pack,REF MDR107002E-4 Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating the bed above its specified weight limit, encountering an obstruction to bed movement, or experiencing jammed components/motor the hand pendant and pendant cords may overheat and, in rare instances, pose a risk of fire. Medline Industries, LP has received a total of (58) complaints associated with reports of pendant sparking, burning, melting, smoking or fire.	FDA Z-1011-2026	Medical Device	High	Jan 28, 2026 Recall: Nov 26, 2025	Details
Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM50, iM60, iM70, iM80 Product Description: The iM series Patient Monitor including iM50, iM60, iM70 and iM80 can perform long-time continuous monitoring of multiple physiological parameters. Also, it is capable of storing, displaying, analyzing and controlling measurements, and it will indicate alarms in case of abnormalities so that doctors and nurses can respond to the patient's situation as appropriate. Component: No As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.	FDA Z-1145-2026	Medical Device	High	Jan 28, 2026 Recall: Oct 24, 2025	Details
Rifton Equipment, Low Base TRAM. Model/Catalog Number: K320. The TRAM is a powered lift device for transferring clients in a seated position or assisting in a sit-to-stand transfer and gait training. The low base variant includes smaller casters and lower base frame so that the legs fit underneath beds. Potential for fraying on the body support strap.	FDA Z-1138-2026	Medical Device	High	Jan 28, 2026 Recall: Dec 18, 2025	Details
Brand Name: EDAN Product Name: Fetal & Maternal Monitor Model/Catalog Number: F6, F9, F6 Express, F9 Express Product Description: The devices are bedside fetal and maternal monitors, which are used to monitor the physiological parameters of pregnant women including the fetus from 28 weeks gestation. The devices may be used antepartum as well as during labor and delivery. Component: No As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.	FDA Z-1141-2026	Medical Device	High	Jan 28, 2026 Recall: Oct 24, 2025	Details
RayStation/RayPlan. Model/Catalog Number: 10.1. Software Version: RayStation/RayPlan 10B. Radiation Therapy Treatment Planning System Potential for the invalidation for calculated radiation dose does not work as intended for certain Regions of Interest (ROIs). This issue occurs for some ROI(s) which have no contours and either have a material override defined, or are of type Bolus, Fixation, or Support. In these cases, adding geometry to the ROI, subsequently modifying geometry, or removing the material override does not invalidate dose as intended.	FDA Z-1102-2026	Medical Device	High	Jan 28, 2026 Recall: Nov 28, 2025	Details
Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Bag Model/Catalog Number: 490127 Software Version: N/A Product Description: The Ion Endoluminal System is a robotically assisted platform for minimally invasive peripheral lung biopsy. Ion consists of a System Cart and Controller that are used to navigate a flexible Catheter within the pulmonary tract using endoscopic visualization for diagnostic and therapeutic procedures. The Ion Fully Articulating Catheter (referred to as the Catheter) consists of the housing, sensor, input discs, shaft, tool channel, and tip. The Catheter is Due to probe bags that may have a compromised or incomplete sterile pouch seal.	FDA Z-1134-2026	Medical Device	High	Jan 28, 2026 Recall: Dec 4, 2025	Details
The LDL-Cholesterol assay is comprised of two distinct phases. In phase one a unique detergent solubilizes cholesterol from non-LDL- lipoprotein particles. This cholesterol is consumed by cholesterol esterase, cholesterol oxidase, peroxidase and 4- aminoantipyrine to generate a colorless end product. In phase two a second detergent in reagent 2 releases cholesterol from the LDL lipoproteins. This cholesterol reacts with cholesterol esterase, cholesterol oxidase and a chromogen system to yield a blue color complex which can be measured bichromatically at 540/660nm. The resulting increase in abs Beckman Coulter identified that LDL Cholesterol OSR6x96 is not meeting the performance claim listed in the Instructions for Use (IFU). LDL Cholesterol reagent showed clinically significant interference due to triglyceride concentration up to 1500 mg/dL may cause a maximum positive bias of up to 28.8% in low LDL Cholesterol samples (concentration 80 mg/dL) and up to 11.02% in high LDL Cholesterol samples (concentration 160mg/dL).	FDA Z-1135-2026	Medical Device	High	Jan 28, 2026 Recall: Dec 8, 2025	Details
Mazor X robotic guidance system REF: TPL0059 Software errors that can result in incorrect surgical instrument positioning during spinal surgery.	FDA Z-1122-2026	Medical Device	High	Jan 28, 2026 Recall: Dec 10, 2025	Details
Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius Plate 6Hd/10Shaft/Left/Std/139mm Model/Catalog Number: 02.426.681S Product Description: 2 Column Distal Radius Plate - 6 Head, 10 Shaft, Standard Left - 139mm The supplier manufactured anatomical left plates with an incorrect thread orientation.	FDA Z-1131-2026	Medical Device	High	Jan 28, 2026 Recall: Dec 19, 2025	Details
Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: X8, X10, X12 Product Description: The X8 X10 X12 Patient Monitor (hereinafter called X series) can perform long-time continuous monitoring of multiple physiological parameters. Also, it is capable of storing, displaying, analyzing and controlling measurements, and it will indicate alarms in case of abnormity so that doctors and nurses can deal with them in time. Component: No As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.	FDA Z-1148-2026	Medical Device	High	Jan 28, 2026 Recall: Oct 24, 2025	Details
Patient Information Center iX; Software Version Number: 4.5.0 A recent software (SW) patch modifies Mobile Event Notification filter settings without providing any indication to the user when upgrading the system.	FDA Z-1156-2026	Medical Device	High	Jan 28, 2026 Recall: Dec 22, 2025	Details
Brand Name: EDAN Product Name: Central Monitoring System Model/Catalog Number: MFM-CMS Product Description: MFM-CMS is a central monitoring system product, which can connect and manage information from EDAN medical devices. MFM-CMS offers central management for monitoring information from the medical devices. All these collected information can be displayed, printed, alarmed and recorded. Component: No As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.	FDA Z-1150-2026	Medical Device	High	Jan 28, 2026 Recall: Oct 24, 2025	Details
Allwell Angioplasty Pack REF: IS-30-B1/B Inflation device handle may detach from the syringe during procedure.	FDA Z-1129-2026	Medical Device	High	Jan 28, 2026 Recall: Dec 4, 2025	Details
TS-10/TS-10H Tube Sorter, automatic sorting system for sorting barcoded sample tubes, Catalog Number BN168792, running software versions 00-17 Under specific conditions, the lift's electromagnetic holding force may disengage unexpectedly, allowing unintended downward movement of the lift.	FDA Z-1136-2026	Medical Device	High	Jan 28, 2026 Recall: Dec 15, 2025	Details
Brand Name: MicroPort Product Name: HIPTURN FEM HEAD TRIAL 36MM REUSABLE Model/Catalog Number: HTHT0036 Software Version: N/A Product Description: HIPTURN FEM HEAD TRIAL 36MM REUSABLE Due to products not having FDA Premarket authorization to be distributed within the United States.	FDA Z-1133-2026	Medical Device	High	Jan 28, 2026 Recall: Dec 19, 2025	Details
Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number: iM3s, iM3As, iM3Bs, iHM3s Product Description: The iM3s series vital signs monitors including iM3s/iM3As/iM3Bs/iHM3s are intended to be used for measuring, storing, reviewing of, and generating prompts for multiple physiological parameters of adults and pediatrics. Component: No As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.	FDA Z-1144-2026	Medical Device	High	Jan 28, 2026 Recall: Oct 24, 2025	Details
Merit Medical , Custom Procedure Kit Reference Numbers: K12T-04270A K12T-07956 K12T-10922B Inflation device handle may detach from the syringe during procedure.	FDA Z-1128-2026	Medical Device	High	Jan 28, 2026 Recall: Dec 4, 2025	Details

Showing 4,651 - 4,675 of 4,975 product recalls

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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

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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.

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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.

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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.

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