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.
Start with the product name or brand. If the list is too broad, search the exact UPC, lot code, model number, date code, NHTSA campaign number or official recall number printed on the notice or label.
Results help you find a possible match quickly. Before you stop use, discard, return or repair anything, open the official notice and confirm every affected detail.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
|
Missing Door Handle Lock/FMVSS 206
Orange EV (OEV) is recalling certain 2018-2023 T-Series Pure Electric and 2024-2026 e-TRIEVER terminal trucks. The driver's side door handles may be missing a lock. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 206, "Door Locks and Door Retention Components." A door that cannot be locked may open unexpectedly during a crash, increasing the risk of injury.
|
NHTSA
26V102000
|
Vehicle | High |
Feb 20, 2026
Recall: Feb 20, 2026
|
Details |
|
High Voltage Battery Fire Risk
Volvo Car USA, LLC (Volvo Car) is recalling certain 2025 EX30 vehicles. The high voltage battery may experience a short circuit and overheat. A high voltage battery that overheats increases the risk of a fire.
|
NHTSA
26V103000
|
Vehicle | Unknown |
Feb 20, 2026
Recall: Feb 20, 2026
|
Details |
|
Trailer Lighting and Brakes May Not Function/FMVSS 108
Ford Motor Company (Ford) is recalling certain 2021-2026 F-150, 2022-2026 F-250 SD, F-350 SD, F-450 SD, F-550 SD, Maverick, 2024-2026 Ranger, 2023-2026 F-600 SD, 2022-2027 Lincoln Navigator, Expedition, and 2026 E-Transit vehicles. When towing a trailer, the integrated trailer module (ITRM) may lose communication with the vehicle, possibly causing a loss of brake and turn signal lights, or a loss of brake function. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, " Lamps, Reflective Devices, and Associated Equipment." Trailer lights or brakes that do not function can reduce the driver’s ability to control the trailer and decrease the trailers visibility to other road users, increasing the risk of a crash.
|
NHTSA
26V104000
|
Vehicle | High |
Feb 20, 2026
Recall: Feb 20, 2026
|
Details |
|
Ajinomoto Foods North America, Inc. Recalls Chicken Fried Rice Products Due to Possible Foreign Matter Contamination
Editor’s Note: Mar. 9, 2026 – The product list in the expanded recall (See Recall 005-2026-EXP ) was updated to reflect that products with the listed lot numbers, regardless of best-by date, are subject to the recall. View full product list . View all labels . Editor’s Note: Mar. 3, 2026 – Ajinomoto Foods North America, Inc., expanded its recall on March 3, 2026 (See Recall 005-2026-EXP ). The establishment recalled approximately 33,617,045 additional pounds of various ready-to-eat and not ready-to-eat chicken and pork fried rice, ramen, and shu mai dumpling products, for a combined total of 36,987,575 pounds subject to the recall. View full product list . View all labels . WASHINGTON, FEB. 19, 2026 – Ajinomoto Foods North America, Inc., a Portland, Ore. establishment, is recalling approximately 3,370,530 pounds of frozen not ready-to-eat (NRTE) chicken fried rice products that may be contaminated with foreign material, specifically glass, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The NRTE chicken fried rice items were produced between September 8, 2025, and November 17, 2025. The following products are subject to recall [ view labels ]: 1.53-kg. cardboard packages containing 6 bags of frozen “AJINOMOTO YAKITORI CHICKEN WITH JAPANESE-STYLE FRIED RICE” with BEST BEFORE/MEILLEUR AVANT dates 26 SE 09 through 26 NO 12. 20-oz. (1 lb. 4 oz.) plastic bag packages containing frozen “TRADER JOE’S Chicken Fried Rice with stir fried rice, vegetables, seasoned dark chicken meat and eggs” with BEST BY dates 9/8/2026 through 11/17/2026. The products subject to recall bear establishment number P-18356 inside the USDA mark of inspection. The Trader Joe’s item was shipped to Trader Joe’s retail locations nationwide. The Ajinomoto item was exported only to Canada. The problem was discovered after the establishment notified FSIS that it received four consumer complaints regarding glass found in product. There have been no confirmed reports of injury due to consumption of this product. Anyone concerned about an injury should contact a healthcare provider. FSIS is concerned that some product may be in retailers’ or consumers’ freezers. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls . Members of the media with questions about the recall can contact Corporate PR at [email protected] or call (909) 477-4800. Consumers with questions about the recall can contact Consumer Affairs, Ajinomoto Foods North America, at (855) 742-5011 or email at [email protected] . Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to [email protected] . For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/ .
|
FSIS
005-2026
|
Food | High |
Feb 19, 2026
Recall: Feb 19, 2026
|
Details |
|
Exterior Driver Side Mirror May Detach
Prevost Car (US) Inc. (Prevost) is recalling certain exterior driver side mirrors with part number 990648. The mirror exhibits excessive play and may detach. A detached mirror can reduce the driver's visibility and become a road hazard for other vehicles, increasing the risk of a crash.
|
NHTSA
26E008000
|
Vehicle | High |
Feb 19, 2026
Recall: Feb 19, 2026
|
Details |
|
Exterior Driver Side Mirror May Detach
Prevost Car (US) Inc. (Prevost) is recalling certain 2026 H3-45 and H3-45 VIP vehicles equipped with aftermarket exterior driver side mirrors. The mirror exhibits excessive play and may detach. A detached mirror can reduce the driver's visibility and become a road hazard for other vehicles, increasing the risk of a crash.
|
NHTSA
26V095000
|
Vehicle | High |
Feb 19, 2026
Recall: Feb 19, 2026
|
Details |
|
A/C Wiring Harness May Short-Circuit
BMW of North America, LLC (BMW) is recalling certain 2025 M5 Sportswagon, 2025-2026 M5, 2024-2025 750e xDrive, 2025-2026 550e xDrive, 2023-2025 I7, 2023-2025 7 Series, 2024-2026 i5, and 5 Series vehicles. The electrical wiring harness for the air conditioning system may become damaged during replacement of the cabin air filter. A damaged wiring harness can short-circuit, increasing the risk of a fire.
|
NHTSA
26V096000
|
Vehicle | Unknown |
Feb 19, 2026
Recall: Feb 19, 2026
|
Details |
|
Panoramic Sunroof Side Trim May Detach
Jaguar Land Rover North America, LLC (Land Rover) is recalling certain 2023-2026 Range Rover Sport and Range Rover vehicles. The panoramic sunroof side finisher trim may not be properly secured and can detach. A detached panoramic sunroof side trim can become a road hazard, increasing the risk of injury or crash.
|
NHTSA
26V097000
|
Vehicle | High |
Feb 19, 2026
Recall: Feb 19, 2026
|
Details |
Vive Health Recalls Adult Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails
This recall involves Vive Health Bed Rails, model LVA1024 and LVA3031BLK. The model LVA1024 bed rail comes in a white frame with a black handle and measures 20 inches wide by 32 inches tall. The model LVA3031BLK bed rail comes in a black frame with a black handle and measures 13 inches wide by 18 inches tall.
|
CPSC
10617
|
Consumer Product | High |
Feb 19, 2026
Recall: Feb 19, 2026
|
Details |
SAMIT Youth Multi-Purpose Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets; Sold on Amazon by SAMIT Outdoor
This recall involves SAMIT multi-purpose helmets for children. The recalled helmets were sold in one size and fit a head circumference of about 21 to 23 inches. The helmets are sold in "crack" blue, "crack" red, and "crack" black with a cracked paint design. They were also sold in pure black. The helmets have gray padding, black straps, a black and red buckle with a black chin strap, and a black plastic knob at the back of the helmet for adjusting the fitting.
|
CPSC
10623
|
Consumer Product | High |
Feb 19, 2026
Recall: Feb 19, 2026
|
Details |
Prismatic 3D Prints Recalls Book Nooks Due to Risk of Serious Injury or Death Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries and Statute for Battery Packaging
This recall involves Prismatic 3D Prints Book Nooks with Lights. The book nooks are bookshelf decorations meant to be placed in between books. The book nooks come in three designs: Fantasy Window, Gothic Cathedral Window, and Gothic Cathedral Window that are a set of three. The book nooks were sold in a variety of different colors for the frame and window. Frame colors include antique gold, pewter, black granite, white marble, and black. Window colors include purple, red, yellow, green, and blue. The base of the book nooks has a circular recess behind the window for holding spare CR2032 coin cell batteries. The words "extra battery" is embedded in the plastic in the recess.
|
CPSC
10622
|
Child/Baby | High |
Feb 19, 2026
Recall: Feb 19, 2026
|
Details |
Meijer Recalls Lullaby Lane and MCS Children's Sleepwear Due to Burn Hazard; Violates Mandatory Standard for Children's Sleepwear
This recall involves 10 different styles in various colors and patterns of 12-, 18-and 24-month size MCS and Lullaby Lane branded one-piece footed sleepwear. The brand, size and "Made in Thailand" are printed on the neck of the garment. The sleepwear has the following style number located on a sewn-in, side-seam label: Brand Style/Name MCS 7903815 - Heart MCS 7903816 - XOXO MCS 7903824 - Lucky Shamrock MCS 7903830 - Bunny Lullaby Lane 7904011 - Airplane; Animal Print; Animals; Apples; Camping; Daisies; Dinos; Duckies; Elephants; Forest; Highland Cow; Safari Lilac; Safari White; Sheep; Toile Floral; Bees Lullaby Lane 7904012 - Meadow; Sharks; Star and Moon; Strawberries Lullaby Lane 7904013 - Chalk Blue; Green; Heather Grey; Pastel Lilac; Pink A Boo; Powder Blue MCS 7904907 - Beige Heather Halloween Lullaby Lane 7905217 - Dinos Blue; Dinos Pink; Fair Isle; Heart; Multi Check; Penguin Pink; Penguin Iced Aqua; Polar Bear; Trees Lullaby Lane 7905217 - Buffalo Check; Reindeer Heads; Gingerbread; Trees Lullaby Lane 7905218 - Arctic Scene; Bows MCS 7905646 - Cupids Bows; Shamrocks
|
CPSC
10621
|
Child/Baby | Unknown |
Feb 19, 2026
Recall: Feb 19, 2026
|
Details |
Joly's Recalls 80% Vinegar Due to Risk of Serious Injury or Death from Poisoning and Chemical Burns; Violates FHSA Labeling Requirements
This recall involves Joly's 80% Vinegar (32-ounce, pack of two). The vinegar comes in a white capped transparent bottle with an orange and red label with white lettering that has "Joly's" brand, "80% Vinegar" and "Dilutes to 5 Gallons". There are no other markings on the container.
|
CPSC
10619
|
Consumer Product | High |
Feb 19, 2026
Recall: Feb 19, 2026
|
Details |
JJGoo LED Balloon Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries
This recall involves JJGoo- branded balloon lights. The recalled, submersible lights were sold in packs of 100 LED color-changing lights. Each multi-color, blinking light measures about 0.6 inches in diameter and has 200 preinstalled LR41 batteries. "MY1005E-Colorfu1-100" is printed on a label on the product packaging.
|
CPSC
10620
|
Child/Baby | High |
Feb 19, 2026
Recall: Feb 19, 2026
|
Details |
Huaker Magnetic Balls and Rods Sets Recalled Due to Risk of Serious Injury or Death from Choking; Violates the Small Ball Ban
This recall involves Huaker Magnetic Balls and Rods sets. The sets include 88 pieces and come in a plastic box with a handle. "Magnetic Sticks" and "Model:20A-13" are printed on the box. There are no identifying marks on the magnetic toys.
|
CPSC
10618
|
Child/Baby | High |
Feb 19, 2026
Recall: Feb 19, 2026
|
Details |
|
Spectral CT 7500 on Rails; Product Code (REF): 728334;
As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners are not torqued to specification, the rotor or rotor parts may become unsecured or displaced. While there has been no reported or observed event of expelled parts during gantry rotation, unsecured rotor parts may potentially be expelled.
|
FDA
Z-1318-2026
|
Medical Device | High |
Feb 18, 2026
Recall: Jan 7, 2026
|
Details |
|
Medline medical convenience kits packaged as: MERCY CIRCUMCISION TRAY, Kit SKU CIT6135B
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
|
FDA
Z-1336-2026
|
Medical Device | High |
Feb 18, 2026
Recall: Dec 24, 2025
|
Details |
|
Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE Catheter 9F x 90cm D087031RH 20197344019554¿
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025
|
FDA
Z-1323-2026
|
Medical Device | High |
Feb 18, 2026
Recall: Dec 22, 2025
|
Details |
|
Medline medical convenience kits packaged as: ADULT CATH SECUREMENT DRSG, Kit SKU DYNDC3109
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
|
FDA
Z-1327-2026
|
Medical Device | High |
Feb 18, 2026
Recall: Dec 24, 2025
|
Details |
|
Medline medical convenience kits packaged as: BLOOD CULTURE KIT NS, Kit SKU DYNDH2088
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
|
FDA
Z-1333-2026
|
Medical Device | High |
Feb 18, 2026
Recall: Dec 24, 2025
|
Details |
|
Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheters: Livewire Steerable Electrophysiology Catheter,10 Elec. 2-5-2mm 401582RH 401940RH; Livewire Steerable Electrophysiology Catheter,20 Elec. 2-10-2mm 401904RH; Livewire Steerable Electrophysiology Catheter,20 Elec. 2-5-2mm 401914RH; Livewire Steerable Electrophysiology Catheter,20 Elec. 2-8-2-60-2-8-2mm 401932RH; Livewire Steerable Electrophysiology Catheter,8 Elec. 2-2-2mm 401652RH;
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025
|
FDA
Z-1321-2026
|
Medical Device | High |
Feb 18, 2026
Recall: Dec 22, 2025
|
Details |
|
1) UNIVERSAL KIT, Kit SKU DT22010B; 2) VAD ACCESS KIT, Kit SKU DT22790C; 3) VAD ACCESS KIT, Kit SKU DT22790C; 4) PROCEDURE TRAY, Kit SKU DYNDA2966A; 5) PROCEDURE TRAY, Kit SKU DYNDA2966A; 6) PEDIATRIC CENTRAL LINE SMALL, Kit SKU DYNDC2208C; 7) PORT DRESSING KIT, Kit SKU DYNDC3107; 8) NON STERILE DIALYSIS KIT, Kit SKU DYNDH1029C; 9) UMBILICAL TRAY W/3.5&5FR CATH, Kit SKU UVT1250; 10) UMBILICAL VESSEL TRAY, Kit SKU UVT835; 11) HEMODIALYSIS TRAY, Kit SKU VAR101HVAA.
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
|
FDA
Z-1330-2026
|
Medical Device | High |
Feb 18, 2026
Recall: Dec 24, 2025
|
Details |
|
Medline medical convenience kits packaged as: 1) CANCER SERVICE PORT KIT, Kit SKU DT22710; 2) LINE KIT, Kit SKU DYNDA1857A; 3) PICC REMOVAL KIT, Kit SKU DYNDC1978A; 4) PORT ACCESS TRAY, Kit SKU DYNDC2367; 5) NICU CENTRAL LINE TRAY, Kit SKU DYNDC2407B; 6) CVC DRESSING CHANGE W/ TEG CHG, Kit SKU DYNDC3222A; 7) PICC PROCEDURE PACK, Kit SKU DYNJ59067A; 8) PICC PROCEDURE PACK, Kit SKU PHS950205004B.
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
|
FDA
Z-1329-2026
|
Medical Device | High |
Feb 18, 2026
Recall: Dec 24, 2025
|
Details |
|
Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheters: Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter Use on GE Systems 10439072RH; Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter Use on Siemens Systems 10438577RH; Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter, Use on Siemens Systems 10439011RH
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025
|
FDA
Z-1324-2026
|
Medical Device | High |
Feb 18, 2026
Recall: Dec 22, 2025
|
Details |
|
Brevera Breast Biopsy System Disposable 9 Gauge Needle. Biopsy Instrument.
Presence of particulates in affected devices that can be deposited into breast tissue during use.
|
FDA
Z-1314-2026
|
Medical Device | High |
Feb 18, 2026
Recall: Dec 15, 2025
|
Details |
Use brand, product name, UPC, lot code, best-by date, package size, allergen, contamination issue or distribution state.
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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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FDA-regulated foods, drugs, cosmetics and medical devices. FDA notes that not every recall has a press release on the public recalls page.
Meat, poultry and egg product recalls and public health alerts. Check establishment numbers, lot codes, labels and affected states.
Vehicle, tire, equipment and child-seat campaigns. VIN or license plate lookup is needed to know whether your specific vehicle still needs repair.
Use the brand, product name, manufacturer or retailer. If the result list is long, add a code from the label or package.
Read the product description, recall reason, hazard, affected dates, source agency and official recall number before taking action.
Compare the UPC, lot, best-by date, establishment number, model, serial range, color, size, state, retailer and product photo.
The notice may say stop using, do not eat, discard, return for refund, request a repair kit, replace a part or schedule dealer service.
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.
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.
Use campaign results to understand the issue, then verify your VIN, car seat model or tire information with NHTSA or the manufacturer.
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.
A product recall is a safety or compliance notice saying a product may need to be corrected, removed, returned, repaired, replaced, refunded or discarded.
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.
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.
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.
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.
Yes. Lot codes are especially useful for food, drug, cosmetic and pet food recalls because only certain production batches may be affected.
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.
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.