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

Latest Product Recall Matches

Showing 4,526 - 4,550 of 4,622 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Modified Floor Plan May Exceed GAWR/FMVSS 120 Forest River bus, LLC (Forest River Bus) is recalling certain 2025-2026 Trans Tech school buses. The modified seating floor plan may exceed the the rear Gross Axle Weight Rating (GAWR). As such these vehicles fail to comply with the Federal Motor Vehicle Safety Standard (FMVSS) number 120, "Wheels and Rims - Other Than Passenger Cars." Overloading the rear axle may cause loss of vehicle control, increasing the risk of a crash.	NHTSA 26V014000	Vehicle	High	Jan 16, 2026 Recall: Jan 16, 2026	Details
Rearview Camera Image May Not Display/FMVSS 111 Lucid USA, Inc. (Lucid) is recalling certain 2022-2026 Air vehicles equipped with an AD02 package and operating a software version from 2.8.0 through 2.8.16. The rearview camera image may not display when the vehicle is placed in reverse. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 111, "Rear Visibility." A rearview image that does not display reduces the driver's view behind the vehicle, increasing the risk of a crash.	NHTSA 26V017000	Vehicle	High	Jan 16, 2026 Recall: Jan 16, 2026	Details
Instrument Panel Display Failure/FMVSS 101 Hyundai Motor America (Hyundai) is recalling certain Genesis 2025-2026 G80, GV80, 2026 G80 "Electrified," GV60, GV70 "Electrified" and GV70 vehicles. Due to a software error, the instrument panel display may fail. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 101, "Controls and Displays." An instrument panel display that fails to show critical safety information, such as the speedometer or fuel gauge, increases the risk of a crash.	NHTSA 26V019000	Vehicle	High	Jan 16, 2026 Recall: Jan 16, 2026	Details
Rearview Camera Image May Not Display/FMVSS 111 Lucid USA, Inc. (Lucid) is recalling certain 2025-2026 Gravity vehicles operating a software version prior to 3.3.20. The rearview camera image may not display when the vehicle is placed in reverse. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 111, "Rear Visibility." A rearview image that does not display reduces the driver's view behind the vehicle, increasing the risk of a crash.	NHTSA 26V018000	Vehicle	High	Jan 16, 2026 Recall: Jan 16, 2026	Details
Yixing Trading Recalls KEAWIS Crib Mattresses Due to Risk of Serious Injury or Death from Entrapment and Suffocation; Violates Mandatory Standard for Crib Mattresses This recall involves KEAWIS crib mattresses. KEAWIS crib mattresses were sold in white and measure about 38 inches by 24 inches. Model number "XX-BM-01" is printed on a label sewn on the side of the mattress.	CPSC 10560	Child/Baby	High	Jan 16, 2026 Recall: Jan 15, 2026	Details
Ruahouine Hair Growth Serum Bottles Recalled Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Sold on Amazon by Ruahouine This recall involves Ruahouine Hair Growth Serum. The serum comes in 60ml (2.11 fl. oz.) transparent amber dropper bottles. "Ruahouine", "Minoxidil Hair Growth Serum", and "5% Minoxidil With Biotin" are printed on labels wrapped around the bottles.	CPSC 10556	Child/Baby	High	Jan 16, 2026 Recall: Jan 15, 2026	Details
RootStim Recalls Beard Growth Serum Spray Bottles Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging This recall involves RootStim Beard Growth Serums spray bottles. The serums come in black boxes with orange and white lettering and have an orange mustache icon on its front panel. The boxes have "Beard Growth Treatment" and "5% Minoxidil - Biotin & Rice Water" printed on its front, directions and warnings printed on its sides, and "Distributed By RootStim LLC" on the bottom. The bottles are black with black spray cap, transparent top cap, and an orange and black wraparound label bearing the same information as the box.	CPSC 10565	Child/Baby	High	Jan 16, 2026 Recall: Jan 15, 2026	Details
R.X.Y Bicycle Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets This recall involves R.X.Y-branded adult bike helmets. The recalled helmets were sold in one size fitting a head circumference of about 22.44 to 24.41 inches. The helmets are blue with black and have gray padding, black straps with a silver reflective pattern in the center and a black and red buckle with a gray chin strap. The helmets have a black plastic knob at the back of the helmet for adjusting the fitting. Item number "Kx012" is printed on the helmet's instruction manual.	CPSC 10559	Consumer Product	High	Jan 16, 2026 Recall: Jan 15, 2026	Details
Morgan Lane Recalls Children's Pajama Sets Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Flammability Standards for Children's Sleepwear This recall involves Morgan Lane Asher Pajama Sets, Style 816TR in Petal. The recalled children's pajama sets are printed with tiny roses and have blue cotton piping and imitation mother-of-pearl buttons. The pajamas were sold in sizes 2T to 14. "MORGAN LANE" and "PURE COTTON" are printed on labels located in the neck and waistband, and "100% Cotton Made in India" is printed on the side seam label.	CPSC 10562	Child/Baby	High	Jan 16, 2026 Recall: Jan 15, 2026	Details
HEZI Brand Power Strips Recalled Due to Risk of Serious Injury or Death from Electrocution; Sold by HEZI HOME This recall involves HEZI brand power strips. The HEZI power strip has either a gray or yellow metal enclosure with eight receptacles made of black plastic. There are a power and a circuit breaker switch located at the end of the metal enclosure closest to the power cord.	CPSC 10563	Consumer Product	High	Jan 16, 2026 Recall: Jan 15, 2026	Details
Greatale Recalls Self-Feeding Pillows Due to Risk of Serious Injury or Death from Aspiration and Suffocation This recall involves Greatale self-feeding pillows. The recalled self-feeding pillows are made of stuffed fabric and have an elastic sleeve to hold a bottle in front of an infant's face. They were sold in white with angel wing shaped decorations. "Greatale" is on a label sewn into the seam of the pillow.	CPSC 10564	Child/Baby	High	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
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
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

Showing 4,526 - 4,550 of 4,622 product recalls

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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

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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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