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.
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.
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.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
|
Churro Mix; packed in a clear plastic 1lb, 5lb, 50lb unit sizes. no UPC
undeclared allergen ingredient (Egg, Wheat)
|
FDA
H-0117-2027
|
Food | High |
Oct 28, 2026
Recall: Aug 24, 2026
|
Details |
|
Horchata Drink Mix; packaged in 1lb, 5lb, 50lb clear plastic units. No UPC
undeclared allergen ingredient (Milk)
|
FDA
H-0136-2027
|
Food | High |
Oct 28, 2026
Recall: Aug 24, 2026
|
Details |
|
Soybeans; packed in a clear plastic 1lb, 5lb, 50lb unit sizes. No UPC
undeclared allergen ingredient (Soy)
|
FDA
H-0119-2027
|
Food | High |
Oct 28, 2026
Recall: Aug 24, 2026
|
Details |
|
Fritura Rueda Papa / Potato Wheel Snack; packed in a clear plastic 1lb, 5lb, 33lb unit sizes. No UPC
undeclared allergen ingredient (Wheat)
|
FDA
H-0123-2027
|
Food | High |
Oct 28, 2026
Recall: Aug 24, 2026
|
Details |
|
All-Purpose Flour; packaged in 1lb, 5lb, 50lb clear plastic units. No UPC
undeclared allergen ingredient (Wheat)
|
FDA
H-0132-2027
|
Food | High |
Oct 28, 2026
Recall: Aug 24, 2026
|
Details |
|
Voila! juice 100% SQUEEZED ORANGE VOILA! OAKLAND, CA 94601 16 OZ: UPC 701725001074 32 OZ: UPC 701725001081 64 OZ: UPC 701725001098 128 OZ: UPC 701725001104
Product not processed to achieve 5-log pathogen reduction.
|
FDA
H-0165-2027
|
Food | High |
Oct 28, 2026
Recall: Oct 2, 2026
|
Details |
|
Textured Soy Protein; packaged in 1lb, 5lb, 33lb clear plastic units. No UPC
undeclared allergen ingredient (Soy)
|
FDA
H-0155-2027
|
Food | High |
Oct 28, 2026
Recall: Aug 24, 2026
|
Details |
|
10X10 Wheat Snack; packaged in 2lb, 5lb, 33lb clear plastic units. No UPC
undeclared allergen ingredient (Wheat)
|
FDA
H-0159-2027
|
Food | High |
Oct 28, 2026
Recall: Aug 24, 2026
|
Details |
|
Black Sesame Seeds; packed in a clear plastic bag. 1lb, 5lb, 50lb unit size. No UPC
undeclared allergen ingredient (Sesame)
|
FDA
H-0104-2027
|
Food | High |
Oct 28, 2026
Recall: Aug 24, 2026
|
Details |
|
Fritura mixed dry fruit; packed in a clear plastic 1lb, 5lb, 25lb unit sizes. no UPC
undeclared allergen ingredient (Wheat, Yellow #5, Yellow #6)
|
FDA
H-0120-2027
|
Food | High |
Oct 28, 2026
Recall: Aug 24, 2026
|
Details |
|
Special Red Almond Mole Powder; packaged in 1lb, 5lb, 11lb clear plastic units. No UPC
undeclared allergen ingredient (Sesame, Peanuts, Wheat, Soy, Almonds, Walnuts, Yellow#5, Yellow#6, Red#40, Blue#2)
|
FDA
H-0141-2027
|
Food | High |
Oct 28, 2026
Recall: Aug 24, 2026
|
Details |
|
Whole wheat flour; packaged in 1lb, 5lb, 50lb clear plastic units. No UPC
undeclared allergen ingredient (Wheat)
|
FDA
H-0162-2027
|
Food | High |
Oct 28, 2026
Recall: Aug 24, 2026
|
Details |
|
Milk Chocolate Covered Raisins; packaged in 1lb, 5lb, 20lb clear plastic units. No UPC
undeclared allergen ingredient (Milk, Soy)
|
FDA
H-0158-2027
|
Food | High |
Oct 28, 2026
Recall: Aug 24, 2026
|
Details |
|
Jovy Gummy Worms Neon; packaged in 1lb plastic units. UPC 712199083411
undeclared allergen ingredient (Red#40, Yellow#5, Yellow#6, Blue#1)
|
FDA
H-0130-2027
|
Food | High |
Oct 28, 2026
Recall: Aug 24, 2026
|
Details |
|
Direxion Torqueable Microcatheter, NGMC/FATHOM/027/STRAIGHT/1RO/130; Material Number: M001195710
The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridges on nitinol sleeves due to laser cutting misalignment.
|
FDA
Z-0255-2027
|
Medical Device | High |
Oct 28, 2026
Recall: Sep 16, 2026
|
Details |
|
VOCSN+Pro, Model Number:PRT-00490-001, Package PN:PRT-00853-000. used for ventilatory support.
Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of ventilation therapy.
|
FDA
Z-0122-2027
|
Medical Device | High |
Oct 28, 2026
Recall: Sep 17, 2026
|
Details |
|
MEDLINE DRAPE C-SECTION W/POUCH ST 7/CS, Medline Product Number/SKU DYNJP6101
Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
|
FDA
Z-0269-2027
|
Medical Device | High |
Oct 28, 2026
Recall: Sep 9, 2026
|
Details |
|
Techno-Path Multichem AE Unassayed Level 3, REF:AE623X
A routine stability studies have identified a stability drift affecting the Ammonia (NH4+) analyte in specific lots of Multichem AE quality control material. Additional testing confirmed that the labelled shelf-life performance claim for the Ammonia analyte can no longer be supported for the affected lots. This issue is limited to the Ammonia analyte only. The impacted device may cause delay of issuing results to the physician. Delayed recognition and diagnosis of elevated levels may impact in timely treatment of life-threatening levels described within medical toxicity intervention decision points.
|
FDA
Z-0207-2027
|
Medical Device | High |
Oct 28, 2026
Recall: Aug 14, 2026
|
Details |
|
Direxion Torqueable Microcatheter, NGMC/SINGLE/021/STRAIGHT/1RO/130; Material Number: M001195210
The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridges on nitinol sleeves due to laser cutting misalignment.
|
FDA
Z-0224-2027
|
Medical Device | High |
Oct 28, 2026
Recall: Sep 16, 2026
|
Details |
|
VC+Pro Model Number: PRT-00900-001, Package PN:PRT-00973-000. used for ventilatory support.
Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of ventilation therapy.
|
FDA
Z-0124-2027
|
Medical Device | High |
Oct 28, 2026
Recall: Sep 17, 2026
|
Details |
|
Direxion Torqueable Microcatheter, NGMC/SINGLE/021/STRAIGHT/2RO/155; Material Number: M001195330
The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridges on nitinol sleeves due to laser cutting misalignment.
|
FDA
Z-0236-2027
|
Medical Device | High |
Oct 28, 2026
Recall: Sep 16, 2026
|
Details |
|
MEDLINE medical convenience kits labeled as: 1) BIRTHDAY KIT-DOUBLE BASIN-LF, Medline Kit Number/SKU DYNJ16127N; 2) NYGH-DELIVERY PACK-LF, Medline Kit Number/SKU DYNJ27206D; 3) OB/GYN, Medline Kit Number/SKU DYNJ911652.
Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
|
FDA
Z-0276-2027
|
Medical Device | High |
Oct 28, 2026
Recall: Sep 9, 2026
|
Details |
|
V*Home, Model Number: PRT-01444-000, Package PN:PRT-01445-000. used for ventilatory support.
Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of ventilation therapy.
|
FDA
Z-0133-2027
|
Medical Device | High |
Oct 28, 2026
Recall: Sep 17, 2026
|
Details |
|
V+Pro Model Number: PRT-01185-000, Package PN:PRT-01198-000; Model Number: PRT-01185-001, Package PN: N/A; Model Number: PRT-01185-002, Package PN:N/A. used for ventilatory support.
Ventilator's Internal Flow transducer cable connector may disconnect from internal board, potentially resulting in system reboot and interruption of ventilation therapy.
|
FDA
Z-0129-2027
|
Medical Device | High |
Oct 28, 2026
Recall: Sep 17, 2026
|
Details |
|
InterStim SureScan MRI Leads 978A1 & 978B1: LEAD 978A128 ISTM MICRO 28CM SSMRI TINED 978A128 LEAD 978A133 ISTM MICRO 33CM SSMRI TINED 978A133 LEAD 978A141 ISTM MICRO 41CM SSMRI TINED 978A141 LEAD 978B128 ISTM II 28CM SSMRI TINED 978B128 LEAD 978B133 ISTM II 33CM SSMRI TINED 978B133 LEAD 978B141 ISTM II 41CM SSMRI TINED 978B141
Wrong lead or percutaneous extension selected. Use of an incompatible lead or percutaneous extension will prevent the system from working as intended and may result in delay of surgery or need for surgical replacement of the product.
|
FDA
Z-0266-2027
|
Medical Device | High |
Oct 28, 2026
Recall: Sep 8, 2026
|
Details |
Use brand, product name, UPC, lot code, best-by date, package size, allergen, contamination issue or distribution state.
Cars & equipmentSearch campaigns by make, model, year, component or NHTSA number. Use NHTSA's VIN search for vehicle-specific open recall status.
Family safetyCheck cribs, loungers, strollers, toys, formula, baby food and child car seats by brand, model, date code or hazard.
Fresh updatesBrowse new and recently updated notices across consumer products, foods, vehicles, medical devices and household items.
Start broad with the product name, manufacturer, retailer brand or model family. This is usually the fastest way to find a possible notice.
For food, drugs, cosmetics and packaged goods, compare the UPC, lot code, product code, best-by date, use-by date and package size.
For appliances, electronics, toys, furniture and baby products, match the model number, serial range, date code, color, size and retailer listing.
This site can find vehicle recall campaigns. For your exact car, use the official NHTSA VIN lookup to confirm unrepaired recall status.
Consumer products, toys, furniture, appliances, electronics and baby products. CPSC remedy details can change after a notice is first posted.
FDA-regulated foods, drugs, cosmetics and medical devices. FDA notes that not every recall has a press release on the public recalls page.
Meat, poultry and egg product recalls and public health alerts. Check establishment numbers, lot codes, labels and affected states.
Vehicle, tire, equipment and child-seat campaigns. VIN or license plate lookup is needed to know whether your specific vehicle still needs repair.
Use the brand, product name, manufacturer or retailer. If the result list is long, add a code from the label or package.
Read the product description, recall reason, hazard, affected dates, source agency and official recall number before taking action.
Compare the UPC, lot, best-by date, establishment number, model, serial range, color, size, state, retailer and product photo.
The notice may say stop using, do not eat, discard, return for refund, request a repair kit, replace a part or schedule dealer service.
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.
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.
Use campaign results to understand the issue, then verify your VIN, car seat model or tire information with NHTSA or the manufacturer.
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.
A product recall is a safety or compliance notice saying a product may need to be corrected, removed, returned, repaired, replaced, refunded or discarded.
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.
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.
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.
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.
Yes. Lot codes are especially useful for food, drug, cosmetic and pet food recalls because only certain production batches may be affected.
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.
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.