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

Latest Product Recall Matches

Showing 2,001 - 2,025 of 3,085 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
AirClub Convertible Bassinets Recalled Due to Risk of Serious Injury or Death from Fall Hazard; Violates Mandatory Standard for Bedside Sleepers This recall involves AirClub convertible bassinets which convert into a bedside sleeper. The bassinets come in light grey, beige, and purple colors with quilted padding. "Product Model QX-831" is on a label located on the bottom of the convertible bassinets underneath the mattress pad.	CPSC 10672	Consumer Product	High	Mar 27, 2026 Recall: Mar 26, 2026	Details
4our Kiddies Tip Restraint Kits Recalled Due to Tip-Over Hazard; Risk of Serious Injury and Death This recall involves defective plastic tip restraint kits (also referred to as furniture straps) manufactured by 4our Kiddies. The recalled tip restraint kits contain two white plastic brackets/mounts (one for connection to furniture and the other for connection to the wall), a white plastic cable zip tie, two different pairs of screws (one longer than the other) and two drywall anchors. The plastic in the brackets/mounts and the cable zip tie can break or degrade over time, which could lead to furniture tipping over if a consumer interacts with furniture that was secured by the recalled product. CPSC testing revealed that the recalled plastic tip restraints failed to meet the requirements of the industry standard for tip restraints. CPSC's Anchor It! website, www.anchorit.gov/, has educational materials available to the public, including important instructions for properly anchoring furniture to prevent tip-overs.	CPSC 10670	Child/Baby	High	Mar 27, 2026 Recall: Mar 26, 2026	Details
Park Outside: High Voltage Battery Modules May Short Circuit Nissan North America, Inc. (Nissan) is recalling certain 2026 LEAF vehicles. The high voltage battery may have internal damage that can cause a short circuit within the battery module. A short circuit in a high voltage battery module increases the risk of a fire.	NHTSA 26V188000	Vehicle	High	Mar 26, 2026 Recall: Mar 26, 2026	Details
Improperly Sealed Side Curtain Air Bags/FMVSS 226 Chrysler (FCA US, LLC) is recalling certain 2022-2026 Pacifica and Voyager vehicles. The right and left side curtain air bags may have insufficient pressure retention from improperly sealed seams. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 226, "Ejection Mitigation." Air bags with insufficient pressure retention increase the risk of ejection and injury during a crash.	NHTSA 26V189000	Vehicle	High	Mar 26, 2026 Recall: Mar 26, 2026	Details
Improperly Sealed Side Curtain Air Bags/FMVSS 226 Chrysler (FCA US, LLC) is recalling certain Mopar side curtain air bags with part numbers 68224526AJ and 68224527AH. The right and left side curtain air bags may have insufficient pressure retention from improperly sealed seams. As such, this equipment fails to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 226, "Ejection Mitigation." Air bags with insufficient pressure retention increase the risk of ejection and injury during a crash.	NHTSA 26E014000	Vehicle	High	Mar 26, 2026 Recall: Mar 26, 2026	Details
GAWR on Federal Placard May Exceed Tire Load Rating/FMVSS 120 Gillig, LLC (Gillig) is recalling certain 2023-2024 Low Floor transit buses equipped with Michelin X InCity Grip D rear tires. The rear Gross Axle Weight Rating (GAWR) on the federal placard may exceed the tire load rating. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 120, "Wheels and Rims - Other Than Passenger Cars." Referencing an incorrect GAWR can lead to unintentionally overloading the rear tires, increasing the risk of a crash.	NHTSA 26V190000	Vehicle	High	Mar 26, 2026 Recall: Mar 26, 2026	Details
Incorrect Glaze May Reduce Visibility Though Door/FMVSS 205 ABC BUS Inc is recalling certain 1999-2013 Van Hool C2045, 2004-2013 Van Hool T2145, 2013-2022 Van Hool TX45, 2013-2023 Van Hool CX45, and 2016-2022 Van Hool CX35 vehicles. The front entrance door may have the incorrect glaze on the lower curb view window. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 205, "Glazing Materials." The incorrect glaze may reduce the driver's visibility, increasing the risk of a crash.	NHTSA 26V191000	Vehicle	High	Mar 26, 2026 Recall: Mar 26, 2026	Details
Incorrect Weld May Cause Seat Bracket Failure/FMVSS 207/210 Lucid USA, Inc. (Lucid) is recalling certain 2025-2026 Gravity vehicles. The lap belt anchor brackets on the second row seats may have insufficient welds, which can cause bracket failure. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard numbers 207, “Seating Systems” and 210, “Seat Belt Assembly Anchorages.” Seat bracket failure can increase the risk of injury during a crash.	NHTSA 26V192000	Vehicle	High	Mar 26, 2026 Recall: Mar 26, 2026	Details
Disconnected Half-Shaft May Cause Loss of Drive Power Lucid USA, Inc. (Lucid) is recalling certain 2024-2026 Air vehicles equipped with Pure Rear-Wheel Drive. Improperly secured bolts may allow the half-shaft to disconnect from the drive unit. A disconnected half shaft can result in a loss of drive power, increasing the risk of a crash.	NHTSA 26V193000	Vehicle	High	Mar 26, 2026 Recall: Mar 26, 2026	Details
Fuel Hose May Disconnect and Leak Fuel Honda (American Honda Motor Co.) is recalling certain 2025 CB1000SP motorcycles. The fuel feed hose may disconnect from the fuel tank, causing a fuel leak. A fuel leak near the rear tire can increase the risk of a crash or injury. In addition, a fuel leak in the presence of an ignition source increases the risk of a fire.	NHTSA 26V194000	Vehicle	High	Mar 26, 2026 Recall: Mar 26, 2026	Details
Convatec, EsteemBody Drainable Pouch REF:423657 10-35mm Drainable large pouch may leak due to manufacturing issue.	FDA Z-1584-2026	Medical Device	High	Mar 25, 2026 Recall: Feb 16, 2026	Details
Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 5826659-027, 5826659-029, 5826659-032, 5826659-033, 5826659-028, 5826659-034, 5826659-030, 5826659-019, 5826659-022, 5826659-026, 5826659-023, 5826659-031, 5826659-025, 5826659-002, 5826659-021, 5826659-037, 5826659-014, 5826659-016, 5826659-013 There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.	FDA Z-1569-2026	Medical Device	High	Mar 25, 2026 Recall: Jan 30, 2026	Details
Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software Version: Software version 3.2.0.1 Product Description: Welch Allyn Spot Vision Screener VS100, FDA product code name: Refractometer, ophthalmic One unit per package Display screen may unintentionally flicker due to a software issue. Exposure to flickering lights may induce photosensitive seizure activity in susceptible individuals.	FDA Z-1573-2026	Medical Device	High	Mar 25, 2026 Recall: Feb 18, 2026	Details
Product Name: ID NOW" Influenza A & B 2 Model/Catalog Number: 427-000 Software Version: Not Applicable Product Description: Influenza A/B virus nucleic acid IVD, kit, nucleic acid technique Component: Not Applicable It was confirmed that the impacted lot has a higher occurrence of invalid rates when compared to the product Instructions for Use.	FDA Z-1565-2026	Medical Device	High	Mar 25, 2026 Recall: Feb 9, 2026	Details
Centricity Universal Viewer Software Versions 5.0 SP6 through UV 5.0 SP7.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-026, 2088026-115, 2088026-043, K2042VJED, 2088026-132, 2088026-003, 2088026-110, 2089629-003, 2066908-136, 2066908-150 There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.	FDA Z-1571-2026	Medical Device	High	Mar 25, 2026 Recall: Jan 30, 2026	Details
Brand Name: Aptima HPV Assay Product Name: Aptima HPV Assay Model/Catalog Number: 303585 Product Description: Aptima HPV assay Component: No Due to product exhibiting potential to generate either invalid or false negative results.	FDA Z-1586-2026	Medical Device	High	Mar 25, 2026 Recall: Feb 18, 2026	Details
Cub Pediatric Crib, Model FL19H Cribs sold in the USA are missing two access door warning labels.	FDA Z-1580-2026	Medical Device	High	Mar 25, 2026 Recall: Feb 18, 2026	Details
Artegraft Vascular Graft; REF#: AG740; Labeling mix-up resulting in the incorrect lot outer packaging of product.	FDA Z-1574-2026	Medical Device	High	Mar 25, 2026 Recall: Feb 10, 2026	Details
Convatec, EsteemBody Drainable Pouch REF:423653 10-35mm Drainable large pouch may leak due to manufacturing issue.	FDA Z-1583-2026	Medical Device	High	Mar 25, 2026 Recall: Feb 16, 2026	Details
Convatec, EsteemBody Drainable Pouch REF:423643, 10-45mm Drainable large pouch may leak due to manufacturing issue.	FDA Z-1582-2026	Medical Device	High	Mar 25, 2026 Recall: Feb 16, 2026	Details
Brand Name: STA Liatest D-Di Product Name: STA Liatest D-Di Model/Catalog Number: REF 00515 Product Description: The STA¿ - Liatest ¿ D-Di kit is an immuno-turbidimetric assay for the quantitative determination of D-dimer in venous plasma (in 3.2 % sodium citrate) for use on STA-R¿, STA Compact¿ and STA Satellite¿ analyzers by professional laboratory personnel. The STA¿ - Liatest¿ D-Di is intended for use in conjunction with a clinical pretest probability (PTP) assessment model to exclude pulmonary embolism (PE) and deep venous thrombosis (DVT) in outpatients suspected of PE or DVT. Component: After receiving customer complaints, investigations confirmed the presence of a positive bias in D-Dimer measurements throughout the entire analytical range.	FDA Z-1585-2026	Medical Device	High	Mar 25, 2026 Recall: Feb 5, 2026	Details
Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-406, 2100169-001, 2088026-985, 2088026-971, 2088026-614, 2088026-713, 2088026-994, 2100491-006, 2088026-723, 2088026-308, 2104867-044, 2100491-012, 2088026-962, 2088026-969, 2102676-001, 2088026-936, 2088026-960, K1220JWED, 2088026-806, 2088026-506, 2088026-026, 2088026-970, 2088026-943, 2088026-990, 2088026-940, 2088026-959, 2088026-967, 2088026-989, 2104867-045, 2088026-993, 2088026-306, 2102675-010, There is a potential cybersecurity vulnerability affecting certain versions of Centricity Universal Viewer. User login credentials may be exposed on the local client workstation, which could allow an unauthorized individual to potentially impact system availability and/or manipulate data.	FDA Z-1570-2026	Medical Device	High	Mar 25, 2026 Recall: Jan 30, 2026	Details
Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion Leksell Gamma Knife¿ Icon" Leksell Gamma Knife¿ Elekta Esprit Leksell Gamma Knife¿ (available models Elekta Esprit, Icon", and Perfexion") is a radiosurgery system for use in the stereotactic irradiation of head structures. Surgery is achieved by delivering a prescribed dose as one or more shots of ionizing radiation to the exact site of the target. Due to adapter not being properly aligned or locked in place.	FDA Z-1581-2026	Medical Device	High	Mar 25, 2026 Recall: Feb 18, 2026	Details
MICS3 Angled Sagittal Saw Attachment; Part Number: 210490 A potential issue was identified with the torque strength on the external screws of the MICS3 Angled Sagittal Saw Attachment. These screws, which secure the cover to the Angled Saw Housing, may loosen during use and detach from the attachment.	FDA Z-1572-2026	Medical Device	High	Mar 25, 2026 Recall: Feb 2, 2026	Details
Battery Charging Station; Model: 0998-00-0802; The Battery Charging Station is an optional dual-bay charger used to charge the Cardiosave IABP Lithium- Ion batteries when they are not being used to operate the IABP. Getinge has identified that a protruding screw in the left battery bay limits full insertion of certain batteries and prevents proper charging. The right bay of the Battery Charging Station is not affected by this issue.	FDA Z-1587-2026	Medical Device	High	Mar 25, 2026 Recall: Feb 6, 2026	Details

Showing 2,001 - 2,025 of 3,085 product recalls

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Fresh updates

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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

Consumer products, toys, furniture, appliances, electronics and baby products. CPSC remedy details can change after a notice is first posted.

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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