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 |
|---|---|---|---|---|---|
|
Tail lights May Fail/FMVSS 108
Chrysler (FCA US, LLC) is recalling certain MOPAR tail lights with part numbers 68272126AC, and 68272127AC. The terminals in the tail light wiring harness may be damaged and cause the tail lights to fail. As such, this equipment fails to comply with the requirements of Federal Motor Vehicle Safety Standard number 108, "Lamps, Reflective Devices, and Associated Equipment." Tail lights that fail to illuminate properly reduce the vehicle's visibility to other drivers, increasing the risk of a crash.
|
NHTSA
26E076000
|
Vehicle | High |
Oct 22, 2026
Recall: Oct 22, 2026
|
Details |
VQQQ Gas Patio Heaters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards
This recall involves VQQQ-branded natural gas patio heaters, models VQQQ-A1 and VQQQ-001. They have a bronze pole with a round base and a silver mushroom-shaped top with an adjustable height of 55 inches to 78 inches. A 24-foot-long gray gas hose is attached to the heater's base. The brand and model numbers are printed on the product's purchase receipt.
|
CPSC
11028
|
Consumer Product | High |
Oct 22, 2026
Recall: Oct 22, 2026
|
Details |
FoShanShiNanHaiQuNuoAiTongZhuangShangHang Recalls CIYTI Light-Up Princess Costumes Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys
This recall involves CIYTI Light-Up Princess Costumes. The costumes include a blue dress with a crown and wand that light up, and a remote control. The crowns, scepters, and remote controls contain button batteries. There are no markings on the product. The package has "CIYTI" on the front.
|
CPSC
11032
|
Child/Baby | High |
Oct 22, 2026
Recall: Oct 22, 2026
|
Details |
Costway Recalls Convertible High Chairs Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violate Mandatory Standard for High Chairs
This recall involves Costway high chairs designed to convert into a table and chair set. They were available in several color combinations, including purple and white, red and white, blue and white, and brown and white. There is no tracking information located on the products.
|
CPSC
11030
|
Child/Baby | High |
Oct 22, 2026
Recall: Oct 22, 2026
|
Details |
BAMAMON Recalls LED Projecting Finger Light Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys
This recall involves Bamamon LED Projecting Finger Light toys which contain three button cells batteries. The finger lights come in 32 pieces in a box in red, orange, blue, black, purple, clear, green and yellow. The finger lights project eight space themed patterns such as astronauts, rockets, UFO, galaxy and solar systems printed on labels located on the front of the package.
|
CPSC
11031
|
Electronics | High |
Oct 22, 2026
Recall: Oct 22, 2026
|
Details |
|
Fuel Filter Hoses May Disconnect and Leak Fuel
PACCAR Incorporated (PACCAR) is recalling certain 2022-2023 Kenworth T370, T270, 2022-2027 Kenworth T280, Peterbilt 548, 2023-2027 Kenworth T480, T380, Peterbilt 536, 537, and 2025 Peterbilt 567 vehicles. The remote fuel filter hoses may separate from the fitting, causing a fuel leak and an engine stall. A fuel leak in the presence of an ignition source increases the risk of a fire. An engine stall increases the risk of a crash.
|
NHTSA
26V700000
|
Vehicle | High |
Oct 21, 2026
Recall: Oct 21, 2026
|
Details |
|
FDA
H-0092-2027
|
Food | High |
Oct 21, 2026
Recall: Sep 23, 2026
|
Details | |
|
Holsum Spinach Flour Tortillas Large, 8 count (20 oz.) UPC: 810023430629
Undeclared colors (FD&C Blue No. 1 and FD&C Yellow No. 5)
|
FDA
H-0089-2027
|
Food | High |
Oct 21, 2026
Recall: Sep 28, 2026
|
Details |
|
Stewarts Shops Vanilla chocolate Strawberry Ice Cream 1/2 gallon (1.89 L), UPC: 0 82086 44377 3
Foreign object: May contain pieces of metal
|
FDA
H-0093-2027
|
Food | High |
Oct 21, 2026
Recall: Oct 2, 2026
|
Details |
|
Made From Plants; Daring; Plant Steak Bites; Ready in 4 Mins Microwaveable Pouch; UPC: 86001124319
defective packaging; packaging can rupture/explode during cooking.
|
FDA
H-0091-2027
|
Food | High |
Oct 21, 2026
Recall: Sep 24, 2026
|
Details |
|
Pur Aqua Sparkling Frost Cherry Limeade 17 oz., UPC: 4099100167023
May contain undeclared aspartame.
|
FDA
H-0095-2027
|
Food | High |
Oct 21, 2026
Recall: Oct 7, 2026
|
Details |
|
FDA
H-0090-2027
|
Food | High |
Oct 21, 2026
Recall: Sep 15, 2026
|
Details | |
|
Stewarts Shops Vanilla Heavenly Medley 1/2 Gallon (1.89 L), UPC Codes: 0 82086 44371 1
Foreign object: May contain pieces of metal
|
FDA
H-0094-2027
|
Food | High |
Oct 21, 2026
Recall: Oct 2, 2026
|
Details |
|
RAPICIDE PA Part A High-Level Disinfectant, Model/Catalog Number: ML020116
If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid chemistry may escape from the bottle when the cap is twisted during opening, which could result in user exposure if required personal protective equipment (PPE) is not properly used. Such exposure may result in injury to the user or others in close proximity.
|
FDA
Z-0155-2027
|
Medical Device | High |
Oct 21, 2026
Recall: Sep 21, 2026
|
Details |
|
NeuroStar Advanced Therapy System. Contains the NeuroStar HP Coil Assembly Part Number 81-01000-200. Affects the below NeuroStar Advanced Therapy Systems: 1. NeuroStar 2.0 US; Part Number: 81-01315-000. 2. NeuroStar 3.0 US; Part Number: 81-02315-000. 3. NeuroStar 2.X to 3.2 Upgrade Kit; Part Number: 81-25000-100. 4. NeuroStar Upgrade Kit 3.0 US; Part Number: 81-35000-000. 5. NeuroStar Mobile Console 3.6, 120V, US; Part Number: 81-03315-000. 6. NeuroStar Mobile Console 3.7, 120V, US; Part Number: 81-04315-000. 7. NeuroStar Mobile Console 3.8, 120V, US; Part Number: 81-05315-000.
Cables are not in conformance with the product specifications required in the production of the HP Coil Assembly.
|
FDA
Z-0142-2027
|
Medical Device | High |
Oct 21, 2026
Recall: Aug 24, 2026
|
Details |
|
Medline surgical convenience kits labeled as: 1) EAR, Medline product number/SKU DYNJ909020B; 2) EAR, Medline product number/SKU DYNJ909020A; 3) CAROTID PACK, Medline product number/SKU DYNJ42922C; 4) EAR, Medline product number/SKU DYNJ909020; 5) FEM CAROTID PACK, Medline product number/SKU DYNJ65706; 6) CAROTID CDS-LF, Medline product number/SKU CDS983139B.
Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.
|
FDA
Z-0173-2027
|
Medical Device | High |
Oct 21, 2026
Recall: Sep 2, 2026
|
Details |
|
NaviFlex LW Pusher; Advx Panc. Stent 4/5F; Material Number (UPN): M00535030;
Device was incorrectly manufactured with a guidewire exit port (referred to in the IFU as the RX port), which is not a design feature associated with this device configuration.
|
FDA
Z-0143-2027
|
Medical Device | High |
Oct 21, 2026
Recall: Sep 10, 2026
|
Details |
|
Generic Name: FilmArray¿ Pneumonia Panel Generic Name: FilmArray¿ Pneumonia Panel Model/Catalog Number: RFIT-ASY-0144 (30 pack), RFIT-ASY-0145 (6 pack), FLM1-ASY-0150 (Verification Kits). Verification kit lots (FLM1-ASY-0150) are a sales configuration that consume kits from panel lots (RFIT-ASY-0144). Software Version: N/A Product Description: Multiple-type respiratory pathogen nucleic acid IVD, kit, nucleic acid technique (NAT) Component: N/A
Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results
|
FDA
Z-0148-2027
|
Medical Device | High |
Oct 21, 2026
Recall: Aug 12, 2026
|
Details |
|
TS Misc. Instruments Tray, Triathlon. Catalog Number: 6543-6-519.
Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the 30-minute dry time may lead to a small amount of residual moisture remaining after sterilization.
|
FDA
Z-0167-2027
|
Medical Device | High |
Oct 21, 2026
Recall: Sep 16, 2026
|
Details |
|
BD Phoenix Panel NMIC-306. Catalog Number: 449292.
Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature.
|
FDA
Z-0140-2027
|
Medical Device | High |
Oct 21, 2026
Recall: Aug 13, 2026
|
Details |
|
JenaValve Trilogy Delivery Catheter, Size 23MM REF: TRILOGY-DC-S
Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device.
|
FDA
Z-0134-2027
|
Medical Device | High |
Oct 21, 2026
Recall: Jul 31, 2026
|
Details |
|
Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135 LAP CHOLE DYNJ911660 LAP NISSEN DYNJ911560 UROLOGY LAPAROSCOPIC - 51638 DYNJ908720A
Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures.
|
FDA
Z-0180-2027
|
Medical Device | High |
Oct 21, 2026
Recall: Aug 31, 2026
|
Details |
|
Medline surgical convenience kits labeled as: CABG AUXILIARY PACK, Medline Product Number/SKU DYNJ44925D
Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.
|
FDA
Z-0168-2027
|
Medical Device | High |
Oct 21, 2026
Recall: Sep 2, 2026
|
Details |
|
Scout MD, REF MDS05A-01, MDS05C-01, MDS10C-01 Contents: (1) Scout MD Delivery System, Standard for use with the SCOUT MD Surgical Guidance System, Rx Only, Sterile-EO
The implantable clip may experience difficulties deploying, which could prevent the reflector from functioning as intended during use.
|
FDA
Z-0187-2027
|
Medical Device | High |
Oct 21, 2026
Recall: Aug 27, 2026
|
Details |
|
Vinyl Instrument Guards, labeled as: 1) VENTED INSTRUMENT GUARD 1/16 X 3/4H - WHITE, Model Number 09-1-011; 2) WHITE VENTED INSTRUMENT GUARD 1/16 X 3/4, Model Number 09-1-011; 3) VENTED INSTRUMENT GUARD 5/64 X 3/4 - BLUE, Model Number 09-1-012; 4) BLUE VENTED INSTRUMENT GUARD 5/64 X 3/4, Model Number 09-1-012; 5) VENTED INSTRUMENT GUARD 7/64 X 3/4 - GREEN, Model Number 09-1-013; 6) GREEN VENTED INSTRUMENT GUARD 7/64 X 3/4, Model Number 09-1-013; 7) VENTED INSTRUMENT GUARD 1/8 X 1 - RED, Model Number 09-1-014; 8) RED VENTED INSTRUMENT GUARD 1/8 X 1, Model Number 09-1-014; 9) VENTED INSTRUMENT G
Labeling not compliant with 21 CFR 801 and steam sterilization IFU has been updated.
|
FDA
Z-0188-2027
|
Medical Device | High |
Oct 21, 2026
Recall: Sep 7, 2026
|
Details |
Use brand, product name, UPC, lot code, best-by date, package size, allergen, contamination issue or distribution state.
Cars & equipmentSearch campaigns by make, model, year, component or NHTSA number. Use NHTSA's VIN search for vehicle-specific open recall status.
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Fresh updatesBrowse new and recently updated notices across consumer products, foods, vehicles, medical devices and household items.
Start broad with the product name, manufacturer, retailer brand or model family. This is usually the fastest way to find a possible notice.
For food, drugs, cosmetics and packaged goods, compare the UPC, lot code, product code, best-by date, use-by date and package size.
For appliances, electronics, toys, furniture and baby products, match the model number, serial range, date code, color, size and retailer listing.
This site can find vehicle recall campaigns. For your exact car, use the official NHTSA VIN lookup to confirm unrepaired recall status.
Consumer products, toys, furniture, appliances, electronics and baby products. CPSC remedy details can change after a notice is first posted.
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.