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

Latest Product Recall Matches

Showing 26 - 50 of 4,622 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
EDEN BROTHERS Broccoli Seeds - Calabrese. Sold in packets, Net Wt. 1oz pouches, UPC SVBRO111 -qb2 & 1 Pound pouches UPC SVBRO111 -qb4. Salmonella	FDA H-0177-2027	Food	High	Nov 4, 2026 Recall: Oct 7, 2026	Details
Gluten Free Truly AIP Rustic Bread Mix, 14 oz Products are recalled due to potential undeclared wheat gluten	FDA H-0184-2027	Food	High	Nov 4, 2026 Recall: Sep 8, 2026	Details
Philips Azurion 3 M15. Model Number: 722064, 722222, 722280. Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance characteristics, which may include reduced reliability over time such as loss of imaging functionality or motorized movement, a blank or black display, and/or the inability to store newly acquired images or access previously acquired images.	FDA Z-0293-2027	Medical Device	High	Nov 4, 2026 Recall: Oct 6, 2026	Details
Orthoscan VERSA Accessory Cart, REF: 1000-0021 and Versa Mini C-Arm System, REF: 1000-0020 The accessory cart weldment does not conform to weld dimensional specifications which may result in separation of the monitor arm mounting structure from the cart.	FDA Z-0286-2027	Medical Device	High	Nov 4, 2026 Recall: Sep 3, 2026	Details
Philips Azurion 7 B12. Model Numbers: 722067, 722225. Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance characteristics, which may include reduced reliability over time such as loss of imaging functionality or motorized movement, a blank or black display, and/or the inability to store newly acquired images or access previously acquired images.	FDA Z-0296-2027	Medical Device	High	Nov 4, 2026 Recall: Oct 6, 2026	Details
PENTAX Medical Ultrasound Endoscope. Model Numbers. EG38-J10UT, EG34-J10U. Warnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during the procedure.	FDA Z-0307-2027	Medical Device	High	Nov 4, 2026 Recall: Sep 9, 2026	Details
Philips Azurion 7 M20. Model Numbers: 722079, 722224, 722282. Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance characteristics, which may include reduced reliability over time such as loss of imaging functionality or motorized movement, a blank or black display, and/or the inability to store newly acquired images or access previously acquired images.	FDA Z-0299-2027	Medical Device	High	Nov 4, 2026 Recall: Oct 6, 2026	Details
Carevo, Height-adjustable shower trolley, Model Number BAC1111-01 The side support of the shower trolley may open unintentionally when the handles are not fully locked and additional force is applied during patient handling. If the side support is not fully locked and an additional force is applied by the caregiver on the handle (e.g., during turning or repositioning), the panel may open unintentionally, which can lead to a resident/patient fall and serious injury, such as head injury, fractures, or other trauma resulting from a patient fall.	FDA Z-0315-2027	Medical Device	High	Nov 4, 2026 Recall: Sep 25, 2026	Details
PENTAX Medical Ultrasound Endoscope. Model Number. EG-3270UK. Warnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during the procedure.	FDA Z-0309-2027	Medical Device	High	Nov 4, 2026 Recall: Sep 9, 2026	Details
PENTAX Medical Ultrasound Endoscope. Model Number. EG36-J10UR. Warnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during the procedure.	FDA Z-0306-2027	Medical Device	High	Nov 4, 2026 Recall: Sep 9, 2026	Details
Philips Azurion 3 M12. Model Numbers: 722063, 722221. Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance characteristics, which may include reduced reliability over time such as loss of imaging functionality or motorized movement, a blank or black display, and/or the inability to store newly acquired images or access previously acquired images.	FDA Z-0292-2027	Medical Device	High	Nov 4, 2026 Recall: Oct 6, 2026	Details
Precision Pointer Electromagnetic (8000-050-001) Device may fracture during use at the laser welded joint on the pointer tube. If this happens, loose parts may fall out of the product while the device is inside the patient.	FDA Z-0314-2027	Medical Device	High	Nov 4, 2026 Recall: Sep 24, 2026	Details
PENTAX Medical Water bottle assembly. Model Number. OS-H5. Warnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during the procedure.	FDA Z-0310-2027	Medical Device	High	Nov 4, 2026 Recall: Sep 9, 2026	Details
Model Number: 712010. Potential for the device to fail immediately after an exposure, causing the system to remain stationary.	FDA Z-0288-2027	Medical Device	High	Nov 4, 2026 Recall: Sep 18, 2026	Details
Philips Azurion 7 M12. Model Numbers: 722078, 722223. Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance characteristics, which may include reduced reliability over time such as loss of imaging functionality or motorized movement, a blank or black display, and/or the inability to store newly acquired images or access previously acquired images.	FDA Z-0298-2027	Medical Device	High	Nov 4, 2026 Recall: Oct 6, 2026	Details
ALPHENIX INTERVENTIONAL ANGIOGRAPHY SYSTEM REF: INFX-8000V Due to software issue, X-ray interventional system may experience internal error if F-Store or imagine acquisition is performed while clinical analysis function is use.	FDA Z-0291-2027	Medical Device	High	Nov 4, 2026 Recall: Oct 12, 2026	Details
Philips Azurion 7 B20. Model Numbers: 722068, 722226. Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance characteristics, which may include reduced reliability over time such as loss of imaging functionality or motorized movement, a blank or black display, and/or the inability to store newly acquired images or access previously acquired images.	FDA Z-0297-2027	Medical Device	High	Nov 4, 2026 Recall: Oct 6, 2026	Details
CareLink SmartSync Device Manager App, Model M01A02, Pulse generator, permanent, implantable Software problem has the potential for an inaccurate displayed longevity estimate.	FDA Z-0304-2027	Medical Device	High	Nov 4, 2026 Recall: Sep 24, 2026	Details
PENTAX Medical Ultrasound Endoscope. Model Numbers. EG-3870UTK, EG-3670URK. Warnings added to the IFU for ultrasound endoscopes and water bottle assembly to ensure there is deaerated sterile water in the assembly prior to and during the procedure.	FDA Z-0308-2027	Medical Device	High	Nov 4, 2026 Recall: Sep 9, 2026	Details
ETHILON Nylon Suture, Product Code 697G Nylon suture indicated for use in general soft tissue approximation and/or ligation may have needles with distorted curvature, that may break during use, or could cause additional soft tissue or vessel injury, including tearing or bleeding intraoperatively.	FDA Z-0284-2027	Medical Device	High	Nov 4, 2026 Recall: Sep 23, 2026	Details
EMAG system Model/Catalog Number: 418591/418591U Product Description: Nucleic acid sample preparation instrument IVD, automated Delayed or no result when analyzing clinical samples with EMAG system (ref: 418591/418591U) due to a randomly occurring software error, Error 10003 Heater timeout after updating to recent firmware SP4 Patch 2	FDA Z-0301-2027	Medical Device	High	Nov 4, 2026 Recall: Sep 11, 2026	Details
CareLink SmartSync, RF Head Patient Connector, Model 24967, Pulse generator, permanent, implantable Software problem has the potential for an inaccurate displayed longevity estimate.	FDA Z-0303-2027	Medical Device	High	Nov 4, 2026 Recall: Sep 24, 2026	Details
Nalu TD2 Therapy Disc with firmware, REF: 34014-001, and TD2 Patient Kit, REF: 74011, part of the Nalu Neurostimulation System Therapy Disc (TD) that powers and sends stimulation signals to an Implantable Pulse Generator (IPG), part of a neurostimulation system, has a firmware issue that causes the TD to attempt to restart, then fail, leading it to become non-functional, and if a secondary TD is unavailable, this may lead IPG to become non-functional, thus unable to inhibit transmission of pain signals.	FDA Z-0311-2027	Medical Device	High	Nov 4, 2026 Recall: Sep 30, 2026	Details
ALPHENIX INTERVENTIONAL ANGIOGRAPHY SYSTEM REF: INFX-8000C Due to software issue, X-ray interventional system may experience internal error if F-Store or imagine acquisition is performed while clinical analysis function is use.	FDA Z-0289-2027	Medical Device	High	Nov 4, 2026 Recall: Oct 12, 2026	Details
Philips Azurion S. Model Number: 722285. Solid-State Drives (SSDs) that are not specified in the Medical Device File may have been installed in various PCs. These SSDs may have different performance characteristics, which may include reduced reliability over time such as loss of imaging functionality or motorized movement, a blank or black display, and/or the inability to store newly acquired images or access previously acquired images.	FDA Z-0300-2027	Medical Device	High	Nov 4, 2026 Recall: Oct 6, 2026	Details

Showing 26 - 50 of 4,622 product recalls

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Food safety

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Fresh updates

Latest Product Recalls Today

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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