The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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3151–3175 of 114837

  • SevereFDA (Food)·H-0844-2026·2026-05-27

    Ghirardelli white chocolate ground powder recalled over potential Salmonella contamination

    Ghirardelli Sweet Ground Powder White Chocolate Flavored, 50 oz, is being recalled over potential Salmonella contamination. 13,602 units are affected.

    Product
    GHIRARDELLI SWEET GROUND POWDER WHITE CHOCOLATE FLAVORED NET WT 50oz (3lbs 2oz) 1.41kg Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A. UPC: 747599620386
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Devices)·Z-2218-2026·2026-05-27

    Medtronic DLP Retrograde Cannula Recalls for Sterile Barrier Breach Risk

    Medtronic is recalling certain lots of its DLP Retrograde Cannula (Model 94725), a cardiopulmonary bypass catheter, because the sterile barrier may be breached, potentially allowing contamination. The cannulas were distributed worldwide.

    Product
    Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94725; Cardiopulmonary bypass vascular catheter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V344000·2026-05-27

    Ford Expedition and Lincoln Navigator seat belts may lock inadvertently

    Ford is recalling certain 2018-2022 Expedition and Lincoln Navigator vehicles because the front seat belt pretensioner may inadvertently lock the belt so it cannot retract or extend.

    Product
    FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0818-2026·2026-05-27

    PS Seasoning Save A Lot bind made with recalled milk powder

    PS Seasoning PSW21585 Save A Lot Bind 50# is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination. 992.5 lbs are affected.

    Product
    PSW21585 Save A Lot Bind 50#, Part #: 20009709. PS Seasoning & Spices 216 W Pleasant St Iron Ridge, WI 53035.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V343000·2026-05-27

    Ford Explorer, Ranger and Bronco engines may fail during driving

    Ford is recalling certain 2025-2026 Explorer, Ranger and Bronco vehicles because the engine may fail, resulting in a loss of drive power. 1,536 vehicles are affected.

    Product
    FORD — FORD EXPLORER, RANGER, BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0838-2026·2026-05-27

    Ghirardelli frozen hot cocoa frappe mix recalled over potential Salmonella

    Ghirardelli Perfectly Premium Frappe Mix Frozen Hot Cocoa, 50 oz, is being recalled over potential Salmonella contamination. 18,612 units are affected.

    Product
    GHIRARDELLI PERFECTLY PREMIUM FRAPPE MIX FROZEN HOT COCOA NET WT 50oz (3lbs 2oz) 1.42kg Ingredients: *** nonfat dry milk *** Distributed by Ghirardelli Chocolate Company, San Leandro, CA 94578, U.S.A. UPC: 747599662133
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Food)·H-0814-2026·2026-05-27

    Ellsworth sour cream and onion seasoning made with recalled milk powder

    Ellsworth Sour Cream + Onion Seasoning from PS Seasoning is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination.

    Product
    Ellsworth Sour Cream + Onion Seasoning, Part #: 180000113. Net Wt 25.00 lbs (11.3kg). PS Seasoning & Spices 216 W Pleasant St Iron Ridge WI 53035
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0813-2026·2026-05-27

    Fontana natural parmesan cheese flavor made with recalled milk powder

    Fontana Foods Natural Parmesan Cheese Flavor in 50 lb bags is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination.

    Product
    C7139D1 Natural Parmesan Cheese Flavor, Net Weight: 50 lbs. bags. Item #: 202405. For Further Processing. Fontana Foods, Janesville, WI.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·H-0821-2026·2026-05-27

    Solina bayou blackened ranch seasoning may be contaminated with Salmonella

    Solina Bayou Blackened Ranch Seasoning in 25 lb bags is being recalled because the product has the potential to be contaminated with Salmonella. 327 bags are affected.

    Product
    Solina 6035687 Bayou Blackened Ranch Seasoning, 25lb bag
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·H-0793-2026·2026-05-27

    Flat Belly Bully tonic may be under-processed, allowing botulinum growth

    Flat Belly Bully in 16 oz and 32 oz bottles is being recalled because it may be under-processed, which could allow growth of Clostridium botulinum, and because it lists health claims.

    Product
    Flat Belly Bully 16 oz and 32 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0795-2026·2026-05-27

    VitaminAlly Joint Nourish liquid recalled over manufacturing practice deviations

    VitaminAlly Joint Nourish oral liquid is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen contamination and possible C. botulinum concerns.

    Product
    Joint Nourish. Dosage:2 tablespoons (30mL). Liquid. For Oral use. Packaging: Plastic Bottle. Net Volume:480 ml. Firm Address: VitaminAlly LLC Chandler, AZ 85225.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2210-2026·2026-05-27

    Oncology Kit With Extension Sets May Leak During Infusion Therapy

    ICU Medical is recalling Oncology Kits with extension sets due to potential leaks that could interrupt chemotherapy infusion and expose hazardous substances to patients, caregivers, and pharmacy technicians.

    Product
    Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros; ChemoLock; Syringe Transfer Set w/MicroClave, ChemoLock Port, REF: CL3960
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2227-2026·2026-05-27

    Azurion X-ray System Deaeration Hose May Degrade and Cause Oil Leakage

    The deaeration hose in Philips Azurion X-ray tube cooling units may degrade over time and leak oil, affecting cooling performance and automatically triggering low-dose fluoroscopy mode.

    Product
    Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063), Azurion 3 M15 (722064), Azurion 7 B12 (722067), Azurion 7 B20 (722068), Azurion 7 M12 (722078), Azurion 7 M20 (722079, 722224).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0541-2026·2026-05-27

    Liraglutide Injection Recalled Due to Particulate Matter in Cartridges

    Lupin Pharmaceuticals is recalling Liraglutide Injection due to the presence of white thread-like structures (particulate matter) found in cartridges. The recall affects 217,621 pen injectors distributed nationwide.

    Product
    LIRAGLUTIDE — LIRAGLUTIDE (LIRAGLUTIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2229-2026·2026-05-27

    Integris-Allura X-ray systems with degraded deaeration hoses recalled

    Philips is recalling Integris-Allura X-ray systems because deaeration hoses in X-ray tube cooling units may degrade, causing oil leakage that reduces cooling performance and triggers a system shutdown to low-dose mode.

    Product
    Integris-Allura system; System Code Description (Model Numbers): Integris CV Cesar-Powerpack-Visub-Nicol (722030), Integris Allura 15 & 12 (monoplane) (722043), INTEGRIS Allura 15-12 (biplane) (722044), Integris-Allura 9 (722018), Integris-Allura 9 (Biplane) (722021), Integris…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V341000·2026-05-27

    Toyota and Lexus instrument clusters may fail to display warnings

    Toyota is recalling certain Lexus UX Hybrid, Lexus GX, Toyota Mirai and Land Cruiser Hybrid vehicles because the instrument panel cluster may fail to display certain warnings or indicators.

    Product
    TOYOTA — TOYOTA, LEXUS MIRAI, LAND CRUISER HYBRID, UX HYBRID, GX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0797-2026·2026-05-27

    VitaminAlly womens 50+ multivitamin drops recalled over manufacturing deviations

    VitaminAlly Liposomal Womens 50+ Liquid Multivitamin Drops are being recalled over cGMP deviations that could lead to bacterial pathogen and possible C. botulinum concerns.

    Product
    Liposomal Womens 50+ Liquid Multivitamin Drops. Dosage: 3ml Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2221-2026·2026-05-27

    Medtronic DLP Retrograde Cannula cardiopulmonary bypass catheter

    Medtronic is recalling certain lots of its DLP Retrograde Cannula (Model 94915), a cardiopulmonary bypass vascular catheter, due to potential sterile barrier breach.

    Product
    Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94915; Cardiopulmonary bypass vascular catheter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2217-2026·2026-05-27

    Medtronic DLP Retrograde Cannula 15FR Model 94665 Sterile Barrier

    Medtronic Perfusion Systems is recalling certain lots of the DLP Retrograde Cannula Model 94665 due to potential sterile barrier breach. The product is used in cardiopulmonary bypass procedures worldwide.

    Product
    Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94665; Cardiopulmonary bypass vascular catheter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0802-2026·2026-05-27

    VitaminAlly kids liquid multivitamin drops recalled over manufacturing deviations

    VitaminAlly Liposomal Kids Liquid Multivitamin Drops are being recalled over cGMP deviations that could lead to bacterial pathogen and possible C. botulinum concerns.

    Product
    Liposomal Kids Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2203-2026·2026-05-27

    Swan-Ganz Jr Catheter models recalled due to lumen hub leakage

    Becton, Dickinson and Company is recalling Swan-Ganz Jr Catheters (models SGPT54, SGPT64P, SGPT755P) because the blue proximal injectate lumen hub may leak or break due to manufacturing changes, risking infection, medication loss, and blood loss.

    Product
    Swan-Ganz Jr Catheter, Models: SGPT54, SGPT64P, SGPT755P
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2204-2026·2026-05-27

    Swan-Ganz Pacing Catheter Model D200F7 Recall Due to Leak Risk

    Becton, Dickinson and Company is recalling Swan-Ganz Pacing Catheter Model D200F7 due to a manufacturing defect that may cause the proximal injectate lumen hub to leak or break, potentially leading to infection, medication loss, or blood loss.

    Product
    Swan-Ganz Pacing Catheter, Models: D200F7;
    Category
    Medical Device
    Distribution
    Distributed nationwide