Latest Product Recalls Today

Recent Product Recall Alerts List

Showing 26 - 50 of 4,975 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
Riad's Oliva to Go Spicy Baba Ghanouj contains undeclared sesame	FDA H-0180-2027	Food	High	Nov 4, 2026 Recall: Oct 9, 2026	Details
Gluten Free Truly AIP All Purpose Baking Mix Flour 15.3 oz Products are recalled due to potential undeclared wheat gluten	FDA H-0183-2027	Food	High	Nov 4, 2026 Recall: Sep 8, 2026	Details
Sunny Sky Non-Dairy French Vanilla Creamer, 96oz , bag in box, 3 per case, refrigerate after opening. Product sterility was potentially compromised.	FDA H-0182-2027	Food	High	Nov 4, 2026 Recall: Sep 2, 2026	Details
Gluten Free EAT G.A.N.G.S.T.E.R Pizza Crust and Flat Bread Mix, 5.8oz (165g) & 3.98 lbs. Products are recalled due to potential undeclared wheat gluten	FDA H-0185-2027	Food	High	Nov 4, 2026 Recall: Sep 8, 2026	Details
ZestiGreens Broccoli Seeds for Sprouting & Microgreens; 8 OZ; Heirloom Broccoli Seeds. SKU: X004IOM4AJ ZestiGreens Broccoli Seeds for Sprouting & Microgreens; 16 OZ; Heirloom Broccoli Seeds. SKU: B0D5289F94 Broccoli seeds potentially contaminated with Salmonella	FDA H-0176-2027	Food	High	Nov 4, 2026 Recall: Sep 29, 2026	Details
Riad's Oliva to Go Baba Ghanouj contains undeclared sesame	FDA H-0179-2027	Food	High	Nov 4, 2026 Recall: Oct 9, 2026	Details
Riad's Oliva to Go Hummus contains undeclared sesame	FDA H-0181-2027	Food	High	Nov 4, 2026 Recall: Oct 9, 2026	Details
Miyoko's Creamery European Style Salted Plant Milk Butter, Net Wt. 8 OZ (227G). UPC 857554005773. Distributed By: Prosperity Organic Foods, Inc. Boise, Idaho 83702. Product is perishable and stored refrigerated/frozen. Product is initially packaged in wax paper wrapping and into an SBS carton. Secondary packaging is the corrugated case for shipment, labeled as Miyoko's Creamery Organic European Style Plant Milk Butter, 6 pack, 8 oz units Net Wt 3.0 LB. Product recalled due to yeast, mold, and E. coli.	FDA H-0178-2027	Food	High	Nov 4, 2026 Recall: Sep 11, 2026	Details
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

Showing 26 - 50 of 4,975 product recalls

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Product Recalls Today

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CPSC

Latest Consumer Product Recalls

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FDA

Latest Food And Medical Device Recalls

Recent FDA notices can include Class I, Class II and Class III recalls, market withdrawals, safety alerts, code information and distribution areas.

USDA FSIS

Latest Meat And Poultry Recall Alerts

FSIS alerts cover meat, poultry and egg products, including public health alerts, undeclared allergens, pathogen risks and misbranding issues.

NHTSA

Latest Vehicle Recall Campaigns

New vehicle, tire, equipment and child-seat campaigns include defect summaries, affected units, remedy notes and NHTSA campaign numbers.

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Check The Publish Date First

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Prioritize High-Risk Notices

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Verify The Official Notice

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Latest Product Recalls FAQ

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How often is the latest product recall list updated?

The site syncs official recall sources daily and stores updated records by source agency, dataset and official recall ID.

Why do some recent recalls have older recall dates?

Some agencies publish or classify a recall after the company began the recall. Use both the published date and recall date when reviewing a notice.

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Match the brand, product name, package size, UPC, lot code, best-by date, allergen or contamination issue and distribution area before taking action.

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Yes. Use the risk filter or highest-risk sort to surface recalls marked critical or high risk across all official sources.

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