Official-source recall search for consumers · Updated daily

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

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.

Check The Item You Have

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.

4,975Total recalls
1,134Food recalls
741Vehicle recalls
4,641High risk

Latest Product Recall Matches

Showing 3,226 - 3,250 of 4,622 matching product recalls.
Open Latest Recalls
Product Recall Source Type Risk Date Action
FDA Z-1712-2026
Medical Device High
Apr 15, 2026 Recall: Feb 27, 2026
Details
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. ROBOTIC PACK, Medline SKU # DYNJ58475F; 2. URO/GEN ROBOTIC PACK, Medline SKU # DYNJ60803J.
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
FDA Z-1728-2026
Medical Device High
Apr 15, 2026 Recall: Feb 27, 2026
Details
FDA Z-1780-2026
Medical Device High
Apr 15, 2026 Recall: Mar 5, 2026
Details
FDA Z-1791-2026
Medical Device High
Apr 15, 2026 Recall: Mar 5, 2026
Details
COOK MEDICAL Cook¿ Strange Bile Duct Stone Exploration Set: Reference Part Number C-CSRC-7.5D-40-STRANGE, Order Number G09108
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
FDA Z-1784-2026
Medical Device High
Apr 15, 2026 Recall: Mar 5, 2026
Details
FDA Z-1785-2026
Medical Device High
Apr 15, 2026 Recall: Mar 5, 2026
Details
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: SPECIAL PROCEDURE TRAY, Medline SKU # DYNJ80513B
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
FDA Z-1720-2026
Medical Device High
Apr 15, 2026 Recall: Feb 27, 2026
Details
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: CVOR ANGIOGRAPHY PACK-LF, Medline SKU DYNJ42367B
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
FDA Z-1714-2026
Medical Device High
Apr 15, 2026 Recall: Feb 27, 2026
Details
FDA Z-1716-2026
Medical Device High
Apr 15, 2026 Recall: Feb 27, 2026
Details
FDA Z-1713-2026
Medical Device High
Apr 15, 2026 Recall: Feb 27, 2026
Details
FDA Z-1778-2026
Medical Device High
Apr 15, 2026 Recall: Mar 5, 2026
Details
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. NON VASCULAR PACK, Medline SKU # DYNJ68037C; 2. VEIN, Medline SKU # DYNJ89845; 3. VEIN, Medline SKU # DYNJ89845A.
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
FDA Z-1719-2026
Medical Device High
Apr 15, 2026 Recall: Feb 27, 2026
Details
XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm, Part Number X073-6555-DL.
Units from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is.
FDA Z-1773-2026
Medical Device High
Apr 15, 2026 Recall: Feb 18, 2026
Details
Brake Pedal May Detach from Brake Booster
Volkswagen Group of America, Inc. (Audi) is recalling certain 2019-2023 Audi E-Tron Quattro, 2020-2023 Audi E-Tron Sportback, 2024 Q8 E-Tron, Q8 Sportback E-Tron, SQ8 E-Tron, and SQ8 Sportback E-Tron vehicles. The fastener that connects the brake pedal and the brake booster may have been improperly assembled during manufacturing, which can cause the brake pedal to detach from the brake booster. Brake pedal detachment can cause a loss of brake function and increase the risk of a crash.
NHTSA 26V240000
Vehicle High
Apr 15, 2026 Recall: Apr 15, 2026
Details
Missing Side Reflectors/FMVSS 108
Winnebago Industries, Inc. (Winnebago) is recalling certain 2027 Suncruiser and 2026-2027 Sunflyer motorhomes. The side reflectors may not have been installed. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 108, "Lamps, Reflective Devices, and Associated Equipment." Missing reflectors can reduce the visibility of the vehicle to other drivers, increasing the risk of a crash.
NHTSA 26V241000
Vehicle High
Apr 15, 2026 Recall: Apr 15, 2026
Details
Missing Front Axle Hub Spindle Nut
Ford Motor Company (Ford) is recalling certain 2025-2026 F-59 and F-53 vehicles. The front axle hub assembly may be missing the spindle nut and cotter pin. A missing spindle nut may lead to brake system damage or wheel detachment, resulting in a loss of vehicle control and increasing the risk of a crash.
NHTSA 26V235000
Vehicle High
Apr 14, 2026 Recall: Apr 14, 2026
Details
Loss of Drive Power due to Transmission Misalignment
Ford Motor Company (Ford) is recalling certain 2021-2025 Bronco vehicles. The transmission to transfer case joint may be misaligned due to an incorrectly performed previous repair, which could lead to wear of the transmission output shaft splines and transfer case input splines. Excessive wear of the transmission and transfer case splines may result in a loss of drive power or vehicle rollaway, increasing the risk of a crash.
NHTSA 26V236000
Vehicle High
Apr 14, 2026 Recall: Apr 14, 2026
Details
Unexpected Downshift Can Cause Loss of Control
Ford Motor Company (Ford) is recalling certain 2015-2017 F-150 vehicles. A loss of signal between the transmission range sensor and the powertrain control module can cause the transmission to unexpectedly downshift into second gear. Unexpectedly downshifting into second gear may result in a loss of vehicle control, increasing the risk of a crash.
NHTSA 26V237000
Vehicle High
Apr 14, 2026 Recall: Apr 14, 2026
Details
Sun Visor Wiring May Cause Fire
Ford Motor Company (Ford) is recalling certain 2024-2026 Ranger vehicles. The sun visor or headliner wiring harnesses may be improperly positioned or have excessive tape thickness, which can result in damaged wires. Damaged wires can create an electrical short and cause a fire in the A-pillar area, increasing the risk of injury or a crash.
NHTSA 26V238000
Vehicle High
Apr 14, 2026 Recall: Apr 14, 2026
Details
Incorrect Seating Capacity on Label/FMVSS 110
Jayco, Inc. (Jayco) is recalling certain 2025-2026 Entegra Ethos recreational vehicles. The Occupant and Cargo Carrying Capacity (OCCC) and Tire Loading Information labels state an incorrect number of seat belt equipped seating positions, which can result in unbelted passengers. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 110, “Tire Selection and Rims.” Unbelted passengers may not be properly restrained in a crash, increasing their risk of injury.
NHTSA 26V233000
Vehicle High
Apr 13, 2026 Recall: Apr 13, 2026
Details
Loss of Rear Brakes
Harley-Davidson Motor Company (Harley-Davidson) is recalling certain 2025-2026 FLHC, FXBB, FXLRS, and FXLRST Softail motorcycles. The rear brake line may contact the Body Control Module (BCM), resulting in a hole in the brake line, a brake fluid leak, and loss of the rear brakes. Loss of the rear brakes increases the risk of a crash.
NHTSA 26V234000
Vehicle High
Apr 13, 2026 Recall: Apr 13, 2026
Details
Air Bag Inflator May Rupture or Detach from Steering Wheel
Nissan North America, Inc. (Nissan) is recalling certain 2009-2010 Cube vehicles. The driver’s air bag inflator may rupture or detach from the steering wheel during air bag deployment. A driver's air bag that ruptures or detaches can strike the driver or other occupants, increasing the risk of injury during a crash.
NHTSA 26V230000
Vehicle High
Apr 10, 2026 Recall: Apr 10, 2026
Details
Incorrect Weight Capacity on Label/FMVSS 110
Bentley Motors, Inc. (Bentley) is recalling certain 2026 Bentayga vehicles. The maximum vehicle capacity weight value on the tire placard label is incorrect. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 110, "Tire Selection and Rims." Incorrect weight information may lead to unintentionally overloading the vehicle, increasing the risk of a crash.
NHTSA 26V231000
Vehicle High
Apr 10, 2026 Recall: Apr 10, 2026
Details
Yeeluzan Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Yeeluzan
Yeeluzan Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Yeeluzan
This recall involves Yeeluzan-branded pool drain covers that are sold for use in swimming pools. The pool drain covers measure about 8.7 inches in diameter and weigh 1.7 pounds. They are white and made of ABS plastic and sold in two-packs.
CPSC 10704
Consumer Product High
Apr 10, 2026 Recall: Apr 9, 2026
Details
Vitaquest International Recalls Multiple Iron Supplement Bottles and Packets Due to Risk of Serious Injury or Death from Poisoning to Young Children; Violates Mandatory Standard for Child-Resistant Packaging
Vitaquest International Recalls Multiple Iron Supplement Bottles and Packets Due to Risk of Serious Injury or Death from Poisoning to Young Children; Violates Mandatory Standard for Child-Resistant Packaging
This recall involves Arey, Bari Life, Bird&Be, Biote, Dr. Fuhrman, NuLife, HMR, Bariatric Pal, Noevir, Zenbean and Sakara brand iron-containing dietary supplements without child-resistant packaging. Brand / Product Name Arey Not Today, Grey (60ct and 180ct) 0034I5 Sept. 2027 860007168901 0342B5 Feb. 2027 860007168901 0342B5A Feb. 2027 860007168901 0360G5 July 2027 860007168901 0442H4 Sept. 2026 860007168994 0442H4A Sept. 2026 860007168994 0442H4B Sept. 2026 860007168994 0483G5 July 2027 860007168994 Bari Life Complete Bariatric Vitamin - Watermelon (60ct) 0138G5 July 2028 860012913930 0177D3 April 2026 860012913930 0207A4 Jan. 2027 860012913930 0333K4 Nov. 2027 860012913930 Bird&Be The Prenatal Essentials for Females (30 pkts) 0005K4 Oct. 2026 860010126417 Bird&Be The Power Prenatal for Females (30 pkts) 0006K4 Aug. 2026 860010126479 Bird&Be The Power Prenatal for Females + CoQ10 Boost (30pkts) 0060L4 Aug. 2026 860010126493 Bird&Be Female Fertility Power Prenatal Pack (30 pkts) 0346C5 March 2027 860013460136 0354F5 May 2027 Bird&Be Complete Prenatal Pack (30 pkts) 0342C5 May 2027 860013460174 0345F5 0345F5A 0345F5B Bird&Be Female Fertility Power Prenatal + CoQ10 Pack (30 pkts) 0360F5A June 2027 860013460143 0360F5 June 2027 0350C5 March 2027 Biote Nutraceutical Iron+ (30ct) 0068F5 May 2027 0516K4 0516K4 Jan. 2027 0068F5 Dr. Fuhrman Gentle Prenatal Multivitamin + D3 (120ct) 0091A5 Feb. 2027 829584500061 Dr. Fuhrman Pixie Vites Children's Multivitamin (120ct) 0130K4 Dec. 2026 829584500153 NuLife Advanced Bariatrics Multivitamin Chewable Tablets (60ct) 0041C4 Feb. 2027 746888915028 0248J4 Oct. 2027 746888915028 0248J4A Oct. 2027 746888915028 0305F5 July 2027 746888915028 0342J3 Oct. 2026 746888915028 0363F3 June 2026 746888915028 0363F3A June 2026 746888915028 0416C5 April 2027 746888915028 0440H4 Sept. 2027 746888915028 0521D5 May 2027 746888915028 HMR Multi Daily Vitamin and Mineral Supplement (60ct) 0013H5 July 2027 00709355144413 Bariatric Pal Ultra Multi Bariatric Multivitamin (90ct) 0148I4 Sept. 2026 0038407566232 Noevir Inner Care Premium BioEssentials (120ct) 0134F4 July 2026 N/A Zenbean Kids Café Instant Coffee + Nutrition Latte, Original, Caramel, Chocolate, and Vanilla (30srv) 0028H4 Aug. 2026 810067444910 0051H5 Aug. 2028 850067341338 0052H5 Aug. 2028 850067341314 0050H5 Aug. 2028 850067341321 Sakara The Foundation (30pkts) 0340A5 Sept. 2026 858151008334 0340A5A Sept. 2026 858151008334 0340A5B Sept. 2026 858151008334 0340A5C Feb. 2027 858151008334 0340A5D Feb. 2027 858151008334 0540H4D June 2026 858151008334 Sakara The Foundation: Prenatal (30pkts) 0338A5A Feb. 2027 858151008341 0338A5B Feb. 2027 858151008341.
CPSC 10695
Child/Baby High
Apr 10, 2026 Recall: Apr 9, 2026
Details
Showing 3,226 - 3,250 of 4,622 product recalls

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.