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

Latest Product Recall Matches

Showing 551 - 575 of 3,318 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
1. TNVitamins Ultrapotent Complete Green Superfood Moringa Capsules (120 count) 2. Doctor s Pride Complete Green Superfood Ultra Potent Moringa 10,000 mg (120 capsules) Product may be contaminated with Salmonella.	FDA H-0942-2026	Food	High	Jun 17, 2026 Recall: May 22, 2026	Details
Rollitos de DulceLeche [image] Caramel Rolls The Original, Net Wt. 15 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852454 Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).	FDA H-0920-2026	Food	High	Jun 17, 2026 Recall: Apr 3, 2026	Details
Rollitos de Guava [image] Guava Rolls The Original, Net Wt. 15 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852454 Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).	FDA H-0919-2026	Food	High	Jun 17, 2026 Recall: Apr 3, 2026	Details
Marquesita de Chocolate y Vainilla [image] Delighted Flavored Cakes The Original, Net Wt. 16 oz, packaged in a transparent and rigid plastic clamshell container, one unit per container. KEEP REFRIGERATED. UPC 824790852706 Undeclared colors (Yellow #5, Yellow #6, and/or Red #40).	FDA H-0932-2026	Food	High	Jun 17, 2026 Recall: Apr 3, 2026	Details
CGuard Prime Carotid Stent System, 135cm, 10mmx30mm Model/Catalog Number: CND1030 Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.	FDA Z-2329-2026	Medical Device	High	Jun 17, 2026 Recall: May 1, 2026	Details
EXCOR Pediatric Ventricular Assist Device (VAD) System Blood Pump PU Valves: 10 ml, REF: P10P-001; 30 ml, REF: P30P-001x01 Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures.	FDA Z-2320-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 24, 2026	Details
Merlin" Patient Care System (PCS) software Merlin" PCS 3650 programmer Model 3330 software Software malfunction may occur during pacing capture threshold test of pacemaker resulting in programmer not successfully communicating the command to terminate the test.	FDA Z-2405-2026	Medical Device	High	Jun 17, 2026 Recall: May 12, 2026	Details
Allia IGS 7 Pulse angiographic X-ray system GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrical shock to service personnel performing installation, maintenance, or troubleshooting activities inside the C-FRT cabinet while power is ON.	FDA Z-2316-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 20, 2026	Details
Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-8216.50/1, 1/Pkg; Cannulated Compression Screws for bone fixation The cannulation of the CCS screw is not centered.	FDA Z-2361-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 24, 2026	Details
TDC VELOCE", 25G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT25, 9311.25G01, 9311.25G02, 9311.25K01, 9311.25K02, 9311.25K03, 9625.G0201; An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.	FDA Z-2323-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Plum Solo Precision IV Pump, 40001-0401 Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may potentially lead to under- or over-delivery.	FDA Z-2311-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 29, 2026	Details
Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28 Some units of Aluminum Chloride Gel contain the package insert for Ferric Sulfate Gel. The incorrect insert misidentifies the product and contains different first aid instructions, most critically in that the Ferric Sulfate insert instructs users to induce vomiting in the case of ingestion, while the correct Aluminum Chloride insert instructs users not to induce vomiting.	FDA Z-2400-2026	Medical Device	High	Jun 17, 2026 Recall: May 27, 2026	Details
Brand Name: CGuard Prime Carotid Stent System, 135cm, 9mx40mm Model/Catalog Number: CND0940 Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.	FDA Z-2328-2026	Medical Device	High	Jun 17, 2026 Recall: May 1, 2026	Details
Plum Duo Infusion Pump, 40002-0401 Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may potentially lead to under- or over-delivery.	FDA Z-2312-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 29, 2026	Details
CGuard¿ Prime Carotid Stent System, 135cm, 10mmx40mm Model/Catalog Number: CND1040 Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.	FDA Z-2330-2026	Medical Device	High	Jun 17, 2026 Recall: May 1, 2026	Details
Halyard, Eye Bag Pack. Kit Code: UIEB48-01. Inadvertent distribution of sealed pouches that had not undergone validated sterilization.	FDA Z-2410-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Hintermann Series Talar Implant, Left, Size 2 REF 302112 Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.	FDA Z-2399-2026	Medical Device	High	Jun 17, 2026 Recall: Mar 24, 2026	Details
Orca Single Use Air/Water and Suction Valves, Material Number (UPN) SUV-617-50; The Orca Air/Water Valve is intended to be used to control the air/water function on an endoscope during a GI (gastrointestinal) endoscopic procedure. Boston Scientific is initiating a medical device removal of Orca Sterile, Single Use Air/Water and Suction Valves due to a higher than anticipated occurrence of the suction button sticking.	FDA Z-2413-2026	Medical Device	High	Jun 17, 2026 Recall: May 12, 2026	Details
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW Model/Catalog Number: 7170-14 Product Description: Feeding Tube Kit Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.	FDA Z-2341-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035. System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.	FDA Z-2354-2026	Medical Device	High	Jun 17, 2026 Recall: May 1, 2026	Details
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PULL Model/Catalog Number: 8180-20 Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.	FDA Z-2351-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Bicarby" Dialysate; Model Numbers: RFP-400-G, RFP-401-G, RFP-402-G, RFP-404-G, RFP-407-G, and RFP-456-G; Given the increased number of leaks reported by users, it was determined to be the appropriate course of action to notify users of the potential for the occurrence of Bicarby luer-lock leaks during manipulation of the frangible and tubing when preparing the product for use for treatment. This issue presents the potential of a slip and fall hazard associated with fluid on the floor.	FDA Z-2321-2026	Medical Device	High	Jun 17, 2026 Recall: May 12, 2026	Details
Halyard, Drape Pack. Kit Code: LMDP36-01. Inadvertent distribution of sealed pouches that had not undergone validated sterilization.	FDA Z-2409-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL Model/Catalog Number: 7180-20 Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.	FDA Z-2345-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PULL Model/Catalog Number: 8180-14 Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.	FDA Z-2350-2026	Medical Device	High	Jun 17, 2026 Recall: Apr 30, 2026	Details

Showing 551 - 575 of 3,318 product recalls

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Food safety

Food Product Recall Search

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Vehicle Recall Lookup

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Family safety

Baby Product Recall Alerts

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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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