Recent recall alerts · Updated daily

Latest Product Recalls Today

Track recent product recall alerts from official U.S. sources. Filter by recall date, source agency, risk level and product category to find newly published food, vehicle, baby product, medical device and consumer product recalls.

Find Recent Product Recall Alerts

Search recent recall notices by product name, brand, UPC, lot code, model number, source agency or official recall number.

Recent Product Recall Alerts List

Showing 1,026 - 1,050 of 3,085 matching product recalls.
Product Recall Search
Product Recall Source Type Risk Date Action
FDA Z-2137-2026
Medical Device High
May 20, 2026 Recall: Mar 19, 2026
Details
Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038200; Cardiopulmonary bypass adaptor, stopcock, manifold, or fitting.
Medline has identified the presence of particulate within the fluid path of the Manifolds.
FDA Z-2138-2026
Medical Device High
May 20, 2026 Recall: Mar 24, 2026
Details
FDA Z-2161-2026
Medical Device High
May 20, 2026 Recall: Apr 13, 2026
Details
FDA Z-2179-2026
Medical Device High
May 20, 2026 Recall: Apr 10, 2026
Details
FDA Z-2190-2026
Medical Device High
May 20, 2026 Recall: Apr 10, 2026
Details
FDA Z-2173-2026
Medical Device High
May 20, 2026 Recall: Apr 10, 2026
Details
Revolution Apex Plus, X-ray Computed Tomography, Model Number 5590000-25
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain Revolution Apex, Revolution Ascend, and Revolution CT systems.
FDA Z-2152-2026
Medical Device High
May 20, 2026 Recall: Mar 26, 2026
Details
FDA Z-2168-2026
Medical Device High
May 20, 2026 Recall: Apr 8, 2026
Details
FDA Z-2135-2026
Medical Device High
May 20, 2026 Recall: Mar 19, 2026
Details
FDA Z-2186-2026
Medical Device High
May 20, 2026 Recall: Apr 10, 2026
Details
Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038301; Cardiopulmonary bypass adaptor, stopcock, manifold, or fitting.
Medline has identified the presence of particulate within the fluid path of the Manifolds.
FDA Z-2139-2026
Medical Device High
May 20, 2026 Recall: Mar 24, 2026
Details
Revolution Apex, X-ray Computed Tomography, Model Number 5590000-20
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain Revolution Apex, Revolution Ascend, and Revolution CT systems.
FDA Z-2154-2026
Medical Device High
May 20, 2026 Recall: Mar 26, 2026
Details
Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name: Dexcom ONE+ iOS CGM App Model/Catalog Number: SW14244 Software Version: versions 1.5.0 and 1.6.0 Product Description: Dexcom ONE+ iOS CGM App Component: Dexcom ONE+ Continuous Glucose Monitoring System
A software defect in which a low-priority file I/O check blocks the higher-priority thread responsible for processing estimated glucose values (EGVs) and trend arrows. When the app is running in the background, EGV notifications may queue up and then "replay" sequentially when the user brings the app to the foreground, causing the Glucose Compass to flicker through previous EGVs. In more severe instances, the app may perceive signal loss and deploy signal loss mitigations. This delay in EGV and alert processing creates a risk that users may miss detection of a hypoglycemic or hyperglycemic event, or make treatment decisions based on outdated glucose information.
FDA Z-2165-2026
Medical Device High
May 20, 2026 Recall: Apr 14, 2026
Details
FDA Z-2180-2026
Medical Device High
May 20, 2026 Recall: Apr 10, 2026
Details
FDA Z-2189-2026
Medical Device High
May 20, 2026 Recall: Apr 10, 2026
Details
Edwards EVOQUE tricuspid delivery system REF:9850TDS Sterile EO
Labeling update to provide warning if functionality of the valve replacement delivery system is compromised.
FDA Z-2172-2026
Medical Device High
May 20, 2026 Recall: Mar 27, 2026
Details
FDA Z-2199-2026
Medical Device High
May 20, 2026 Recall: Apr 10, 2026
Details
FDA Z-2170-2026
Medical Device High
May 20, 2026 Recall: Mar 31, 2026
Details
FDA Z-2144-2026
Medical Device High
May 20, 2026 Recall: Mar 24, 2026
Details
FDA Z-2188-2026
Medical Device High
May 20, 2026 Recall: Apr 10, 2026
Details
FDA Z-2194-2026
Medical Device High
May 20, 2026 Recall: Apr 10, 2026
Details
FDA Z-2145-2026
Medical Device High
May 20, 2026 Recall: Mar 24, 2026
Details
FDA Z-2183-2026
Medical Device High
May 20, 2026 Recall: Apr 10, 2026
Details
Diowave Laser System, REF: Diowave 250W
Software update is needed for laser systems, for topical infrared heating to provide temporary relief of minor muscle and joint pain, spasms, stiffness associated with minor arthritis, and to temporarily increase local blood circulation, operating at a maximum average power output of 70W, which is beyond the FDA cleared 60W.
FDA Z-2162-2026
Medical Device High
May 20, 2026 Recall: Jan 9, 2026
Details
ZYMUTEST HIA IgG, in vitro diagnostic ELISA kit, Ref. RK040A
Kits from lot FD1265 had been packaged on 17 October 2024 and put on the market with an outdated flyer (8 October 2024), containing incorrect values for the positive control.
FDA Z-2171-2026
Medical Device High
May 20, 2026 Recall: Apr 1, 2026
Details
Showing 1,026 - 1,050 of 3,085 product recalls

Product Recalls Today

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Recent Product Recall Alerts

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Latest Recalls By Source Agency

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CPSC

Latest Consumer Product Recalls

New alerts for toys, furniture, appliances, electronics, baby products, household goods and products with injury, choking, fire or fall hazards.

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.

What should I check on a recent food recall?

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

Can I get only high-risk recalls?

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