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

Latest Product Recall Matches

Showing 2,426 - 2,450 of 3,085 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
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
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
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
Medline medical convenience kits packaged as: STERILE RESUTURE PACK, Kit SKU DYNDL1980A 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-1335-2026	Medical Device	High	Feb 18, 2026 Recall: Dec 24, 2025	Details
ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 266-01-000-10-N UDI-DI code: 00190376476179; GMDN 12844 The ATEC Navigation Disc Prep Instruments are intended for use in surgical procedures. These instruments are non-sterile or sterile packaged, re-usable or single-use instruments designed to function with the Medtronic StealthStation System and NavLock Tracker. Due a design issue where the navigated array connection geometry is incorrect.	FDA Z-1342-2026	Medical Device	High	Feb 18, 2026 Recall: Jan 2, 2026	Details
Surepulse VS Cap Extra Large REF: SP-163-A1 component of VS Newborn Heart Rate Monitor Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.	FDA Z-1360-2026	Medical Device	High	Feb 18, 2026 Recall: Jan 20, 2023	Details
Intubation Tray (Adult) containing Suction Catheter Kits SKU DYNJAA245B A smaller open suction catheter, the 8 Fr Suction Catheter, may have been packed within the kit instead of the required 14 Fr Suction Catheter. Use of the smaller size catheter may result in hypoxia and/or respiratory failure related to partial or full airway obstruction. Airway obstruction may require immediate emergent medical intervention to prevent respiratory failure or death. Other potential outcomes include prolonged procedure, airway irritation, or prolonged dyspnea.	FDA Z-1313-2026	Medical Device	High	Feb 18, 2026 Recall: Dec 24, 2025	Details
Surepulse VS Cap Extra Small REF: SP-159-A1 component of VS Newborn Heart Rate Monitor Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.	FDA Z-1356-2026	Medical Device	High	Feb 18, 2026 Recall: Jan 20, 2023	Details
Azurion 5 M20 System Model Numbers: (1)722228, (2)722232, (3)722281(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.	FDA Z-1351-2026	Medical Device	High	Feb 18, 2026 Recall: Jan 26, 2026	Details

Showing 2,426 - 2,450 of 3,085 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.

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

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FDA

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USDA FSIS

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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.

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