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

Latest Product Recall Matches

Showing 4,876 - 4,900 of 4,975 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Energizer Recalls Rechargeable Lanterns Due to Overheating This recall involves the Energizer® Large Power Indicator Lantern. The lantern is a cone-shaped portable light with an opaque lens and "Energizer" displayed on the side. The top portion of the lantern is gray with a large power button on top and a red handle. The model number of the lantern is BGAAL9 and the SKU number is 039800143341 or 039800143334. The model is located on the bottom of the light, on the removable cover that provides access to the charging cord storage area. The SKU is located on the packaging. Only lanterns with a date code of June 2024 located on the base of the unit, are part of this recall. The date code is shown using two circles, one circle has an arrow pointing to the year ("24"), and the other has an arrow pointing to the month ("6").	CPSC 10557	Consumer Product	Unknown	Jan 16, 2026 Recall: Jan 15, 2026	Details
Curtis International Expands Recall of Frigidaire-brand Minifridges Due to Fire and Burn Hazards This recall expansion involves Curtis International 6-can minifridge model EFMIS121. This is in addition to certain minifridges with model numbers EFMIS129, EFMIS137, EFMIS149 and EFMIS175 that were previously recalled. "Frigidaire" is printed on the front of the units. The model and serial numbers are on a label on the back of the minifridge. This recall includes only the serial numbers identified below. The minifridges were sold in red at Target stores. Model Number Serial Number EFMIS121 Between A2001 and A2310	CPSC 10566	Consumer Product	Unknown	Jan 16, 2026 Recall: Jan 15, 2026	Details
BBWOO Baby Loungers Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets This recall involves BBWOO baby loungers. The recalled baby loungers are made of a foam sleeping pad and padded bumpers with a cloth cover and have a ribbon tie at one end. The model number is located on a tracking label stitched on the outside cover. The baby loungers were sold in the following styles and models: Style Model Number Gray Dinosaur BLG26BE Blue Car BLG23BD Green Line BLG04BD Gray Feather BLG01BE Pink Deer BLG17BI Pink Elephant BLG32BI Gray Line BLG04BE Blue CZC44 Gray CZC41 Khaki-Cotton & Velvet CZC43 Red CZC42	CPSC 10558	Child/Baby	High	Jan 16, 2026 Recall: Jan 15, 2026	Details
Adams Manufacturing Recalls Adirondack Patio Chairs Due to Injury and Fall Hazards This recall involves Adirondack-style patio chairs sold under two different brands: Adams RealComfort and StyleWell. The resin chairs with slat backs and seats were sold in blue, dark gray, navy blue, taupe, light blue, lime green and teal. "ML837-15" and the manufacture date of August 2025 are molded on the underside of the recalled chairs. The manufacture date is indicated by a dot on a grid, located at the intersection of column "A" and row "25".	CPSC 10561	Consumer Product	Medium	Jan 16, 2026 Recall: Jan 15, 2026	Details
Improperly Secured Seat Belt Retractor Assemblies Rivian Automotive, LLC (Rivian) is recalling certain 2022-2025 R1T and 2022-2026 R1S vehicles. The bolts that secure the second-row driver and passenger side seat belt retractor assemblies may be improperly tightened. An improperly secured seat belt retractor may not adequately restrain the seat occupant, increasing the risk of injury during a crash.	NHTSA 26V009000	Vehicle	High	Jan 15, 2026 Recall: Jan 15, 2026	Details
Incorrectly Wired Rear Turn Signals/FMVSS 108 Gulf Stream Coach, Inc. (Gulf Stream) is recalling certain 2026 Trail Boss and Ameri-Lite trailers. Wires in the taillight harness may be reversed, causing the turn signals to activate in the opposite direction as the driver intended. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment." Turn signals that fail to indicate the driver's intention to change direction increase the risk of a crash.	NHTSA 26V010000	Vehicle	Critical	Jan 15, 2026 Recall: Jan 15, 2026	Details
Engine Block Heater May Short Circuit and Cause Fire Ford Motor Company (Ford) is recalling certain 2013-2018 Focus, 2013-2019 Escape, and 2015-2016 MKC vehicles equipped with a 2.0L engine. The engine block heater may crack and develop a coolant leak, causing it to short circuit when the block heater is plugged in. An electrical short circuit can increase the risk of a fire.	NHTSA 26V011000	Vehicle	Unknown	Jan 15, 2026 Recall: Jan 15, 2026	Details
Engine Block Heater May Short Circuit and Cause Fire Ford Motor Company (Ford) is recalling certain engine block heaters, with part numbers CV6Z-6A051-CA and CV6Z-6A051-AA, sold as accessory parts for certain 2013-2019 Ford and Lincoln vehicles equipped with 2.0L engines. The engine block heater may crack and develop a coolant leak, causing it to short circuit when the block heater is plugged in. An electrical short circuit can increase the risk of a fire.	NHTSA 26E003000	Vehicle	Unknown	Jan 15, 2026 Recall: Jan 15, 2026	Details
Engine Block Heater May Short Circuit and Cause Fire Ford Motor Company (Ford) is recalling certain 2016-2018 Focus, 2019 Explorer, and 2024 Explorer vehicles. The engine block heater may crack and develop a coolant leak, causing it to short circuit when the block heater is plugged in. An electrical short circuit can increase the risk of a fire.	NHTSA 26V012000	Vehicle	Unknown	Jan 15, 2026 Recall: Jan 15, 2026	Details
Arial 900 MHz Call Station, Model Number CSK200-900, with Firmware version: 1.6.3 Securitas Healthcare has become aware of a firmware issue in the Call Stations in the Affected Lots that may cause Call Stations in the Affected Lots to (1) not transmit a low battery alert to the Arial Wireless Emergency Call System prior to battery failure, or (2) not transmit a low battery alert to the Arial Wireless Emergency Call system at least seven (7) days prior to the battery failing.	FDA Z-1031-2026	Medical Device	High	Jan 14, 2026 Recall: Dec 8, 2025	Details
Codman CereLink ICP Sensor Basic Kit. Catalog Number: 826850. The Codman CereLink ICP Sensor Basic Kit consists of the CereLink ICP Sensor (ICP Sensor) and a 14-gauge Tuohy needle with stylet. The ICP Sensor is a nylon tube with a microminiature strain gauge pressure transducer (sensing element) mounted at one end and an electrical connector at the other end. It is designed for use with a Codman intracranial pressure monitoring device. The ICP Sensor Basic Kit is designed for use with the Codman Cranial Hand Drill. The drill facilitates access to the intraparenchymal area. The drill is also av Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits.	FDA Z-1037-2026	Medical Device	High	Jan 14, 2026 Recall: Dec 12, 2025	Details
Arial 900 MHz Call Station, Model Number CSK200-900MR, with Firmware version: 1.6.3 Securitas Healthcare has become aware of a firmware issue in the Call Stations in the Affected Lots that may cause Call Stations in the Affected Lots to (1) not transmit a low battery alert to the Arial Wireless Emergency Call System prior to battery failure, or (2) not transmit a low battery alert to the Arial Wireless Emergency Call system at least seven (7) days prior to the battery failing.	FDA Z-1032-2026	Medical Device	High	Jan 14, 2026 Recall: Dec 8, 2025	Details
Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor. It was found that the MX40 device could not reconnect to the PIC iX when moving between Radiohead and Trident 1.4 GHz access points if the signal strength changed quickly.	FDA Z-1033-2026	Medical Device	High	Jan 14, 2026 Recall: Dec 12, 2025	Details
Impella 5.5 with SmartAssist¿ S2, Impella 5.5 with SmartAssist S2 Set, AU. Device packaged in incorrect outer box carton.	FDA Z-1030-2026	Medical Device	High	Jan 14, 2026 Recall: Dec 4, 2025	Details
The Elecsys Anti-TSHR immunoassay is a three-step competitive immunoassay with streptavidin-coated microparticles and electrochemiluminescence detection. Patient serum sample is incubated with pretreatment reagent PT1 and the reconstituted PT2 containing a pre-formed immunocomplex of solubilized porcine TSH receptor (pTSHR) and biotinylated anti-pTSHR mouse monoclonal antibody. Issues identified: 1) Results vary by Instrument Platform; 2) Calibrator Lot-to-Lot Variability. Issues may lead to delayed or incorrect diagnosis, as well as delay of treatment or incorrect treatment.	FDA Z-1009-2026	Medical Device	High	Jan 14, 2026 Recall: Nov 21, 2025	Details
Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08 Devices are not suitable for organ transplant.	FDA Z-1002-2026	Medical Device	High	Jan 14, 2026 Recall: Nov 11, 2025	Details
LUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model 10762471 A potential issue associated with LUMINOS Lotus Max and Luminos dRF Max systems with software version VF11 with bucky wall stand for mobile detectors and without ceiling stand .When switching quickly between organ programs (OGPs) the collimation may be incorrect.	FDA Z-0999-2026	Medical Device	High	Jan 14, 2026 Recall: Dec 5, 2025	Details
Philips Tempus Pro Patient Monitor, REF: 00-1004, 00-1007, 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R. USB 2-Channel IBP Module, REF: 01-2017. Used with User/Operator Manual Patient monitor measures Intracranial Pressure (ICP) and Bladder Pressure (BDR) but ICP and BDR measurements have not been tested or validated for accuracy. If healthcare providers base clinical judgment on unvalidated measurements, this could potentially lead to incorrect clinical decisions.	FDA Z-1027-2026	Medical Device	High	Jan 14, 2026 Recall: Nov 26, 2025	Details
Revogene C. difficile, in vitro diagnostic assay intended for use with the Revogene instrument, Catalog Number 410300 The affected lots show a decline in performance over time, which may lead to false-negative results.	FDA Z-1019-2026	Medical Device	High	Jan 14, 2026 Recall: Dec 5, 2025	Details
Brand Name: HFD100 Product Name: Head Fixation Device HFD100 Model/Catalog Number: 119695-000, 119629-000, 119630-000, 113803-000, 113803-600, 113802-000, 113802-600 Software Version: Not Applicable Product Description: The HFD100 Head Fixation Device provides rigid skeletal fixation within the optimal imaging envelope while introducing minimal artifacts in the acquired images. There are two different assemblies for the HFD100. The standard HFD100 is equipped with a table adapter for use with either the operating room table or the angiography table. For sites with a Hill-Rom TruSystem 7500 Hyb Torque screw may crack or separate. If used, an affected screw could lead to inadequate head stabilization, compromised surgical precision, procedural delays, requirement for alternate head fixation methods, and risk of patient injury.	FDA Z-1034-2026	Medical Device	High	Jan 14, 2026 Recall: Dec 8, 2025	Details
Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOG1000-15. Devices are not suitable for organ transplant.	FDA Z-1000-2026	Medical Device	High	Jan 14, 2026 Recall: Nov 11, 2025	Details
Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17. Devices are not suitable for organ transplant.	FDA Z-1001-2026	Medical Device	High	Jan 14, 2026 Recall: Nov 11, 2025	Details
Beckman Coulter UniCel Dxl 800, Part numbers: 973100, A71456, A71457, A25288; Immunoassay Method, Troponin Subunit Beckman Coulter has determined that, due to a potential communication issue, the analyzers listed above may not successfully restart following a standard shutdown, even after multiple attempts. If this issue occurs, the instrument will be unable to complete initialization and transition to Ready mode and the instrument will not process patient samples, QCs or calibrators. This causes delayed results.	FDA Z-1026-2026	Medical Device	High	Jan 14, 2026 Recall: Nov 26, 2025	Details
Beckman Coulter UniCel Dxl 600, Part numbers: A71460, A71461, A30260; Immunoassay Method, Troponin Subunit Beckman Coulter has determined that, due to a potential communication issue, the analyzers listed above may not successfully restart following a standard shutdown, even after multiple attempts. If this issue occurs, the instrument will be unable to complete initialization and transition to Ready mode and the instrument will not process patient samples, QCs or calibrators. This causes delayed results.	FDA Z-1025-2026	Medical Device	High	Jan 14, 2026 Recall: Nov 26, 2025	Details
Medline Hudson RCI Medium Concentration Oxygen Masks: 1041CE MASK,OXYGEN,UND CHIN,MED CO OUS ONLY; HUD1035 O2 MASK,MED CONC,SHORT,PEDI,7' TUB SC; HUD1042 O2 MASK,MED CONC,PEDI,7' TUB SC; HUD1930 O2 MASK,MED CONC,ADULT,7' TUB UC; HUDRHO41U MASK,OXYGEN,MEDIUM-CONCENTRATION,7,SC Firm received multiple complaints regarding tubing disconnecting from oxygen mask. If issue occurs during use, may lead to delay in patient care and patient may experience shortness of breath leading to hypoxia, which may require medical intervention to prevent further respiratory deterioration.	FDA Z-1035-2026	Medical Device	High	Jan 14, 2026 Recall: Nov 21, 2025	Details

Showing 4,876 - 4,900 of 4,975 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.

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This site can find vehicle recall campaigns. For your exact car, use the official NHTSA VIN lookup to confirm unrepaired recall status.

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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.

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