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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2001–2025 of 90251

  • SevereFDA (Devices)·Z-2248-2026·2026-06-10

    BD Quincke spinal trays recalled over Huons bupivacaine quality issues

    BD Spinal Trays with a Quincke 22 G needle are being recalled as a sub-recall of the Huons bupivacaine product recall. 990 units are affected.

    Product
    BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405609.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2276-2026·2026-06-10

    B. Braun spinal needle kits recalled over Huons bupivacaine quality issues

    Spinal needle procedure kits containing Bupivacaine Hydrochloride in Dextrose Injection are being recalled after the drug's manufacturer issued a voluntary recall. 582,030 units are affected.

    Product
    Spinal Needle procedure kits: Material Description (Material Number) 24GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333867); 25GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333862); GOVP24BK 24G PENCAN TRAY W/ BUP & DEXTROS (332607); P24BK 24G PENCAN TRAY W/BUP & DEXTROSE (333868)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2256-2026·2026-06-10

    BD spinal trays recalled as a sub-recall of Huons bupivacaine

    BD Spinal Trays with Whitacre needle, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405671.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0891-2026·2026-06-10

    a2 Platinum infant formula may be contaminated with cereulide toxin

    a2 Platinum Premium infant formula milk-based powder is being recalled over possible contamination with cereulide toxin. 51,202 units were distributed nationwide.

    Product
    a2 Platinum Premium infant formula Milk-based Powder with Iron 31.7oz (900g) Intended use: infant formula (0 12 months). Condition: shelf stable product Type of packaging: metal tin with plastic dust cap. Net weight: 31.7oz (900gm). UPC: 813267020335. Firm name listed on…
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2207-2026·2026-06-10

    Atlan A350 anesthesia workstations may fail during mechanical ventilation

    Atlan A350 anesthesia workstations are being recalled because units either indicated a piston ventilator failure before use or suffered a mechanical ventilation failure during use.

    Product
    Atlan A350. Model Number: 8211500. anesthesia workstation
    Category
    Medical Device
    Distribution
    11 states
  • SevereFDA (Devices)·Z-2252-2026·2026-06-10

    BD Whitacre 24 gauge spinal trays recalled over bupivacaine quality issues

    BD Spinal Trays with a Whitacre 24 G needle, catalog numbers 400868 and 405652, are being recalled as a sub-recall of the Huons bupivacaine product recall. 3,550 units affected.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400868, 405652.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2253-2026·2026-06-10

    BD combined Whitacre and Quincke spinal trays recalled over bupivacaine

    BD Spinal Trays containing both a Whitacre 25 G and a Quincke 22 G needle are being recalled as a sub-recall of the Huons bupivacaine product recall. 290 units affected.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in., BD¿Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405741.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0910-2026·2026-06-10

    Cold prep cream sauce contains dry milk recalled for Salmonella

    Cold Prep Cream Sauce in 20 lb bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.

    Product
    Cold Prep Cream Sauce, 20 lb., packaged in a tied poly bag and packed 1 bag per case, UPC 0039954922458
    Category
    Food
    Distribution
    41 states
  • SevereFDA (Food)·H-0886-2026·2026-06-10

    Sour Cream and Onion Popcorn Seasoning Recalled Due to Potential Salmonella Contamination

    JCB Flavors, LLC is recalling Sour Cream & Onion Flavored Popcorn Seasoning because it may be contaminated with Salmonella.

    Product
    Popping Topping, Sour Cream & Onion Flavored Popcorn Seasoning, Net Wt: 1.6oz. UPC 0 31851-01001 6. Distributed By: Butler's Pantry, 1224 Clark St. Watertown, WI 53094.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·H-0860-2026·2026-06-10

    Malazi Sudanese sesame tahina tested positive for Salmonella

    Malazi 100% Pure Sudanese Sesame Tahina is being recalled after the North Carolina Department of Agriculture notified the firm that the product tested positive for Salmonella.

    Product
    Malazi 100% PURE SUDANESE SESAME Tahina G.W.: 1K.g UPC 6 224011 088244 Produced by: AL-MALAZ COMPANY FOR TRADE AND INDUSTRY Piece No. 110-250 acres area Badr City - Egypt
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2257-2026·2026-06-10

    BD Whitacre 25G spinal trays recalled in Huons bupivacaine sub-recall

    BD Spinal Trays with Whitacre needle 25 G, catalog numbers 405637 and 405707, are being recalled as a sub-recall of the Huons bupivacaine product recall. 5,940 units are affected.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405637, 405707.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0899-2026·2026-06-10

    Hellas Meze Golden Smoked Whole Herring Recall Over Botulism Risk

    Terra Medi LLC is recalling Hellas Meze Golden Smoked Whole Herring due to potential contamination with Clostridium botulinum. The product was distributed in MA, NJ, IL, and NY.

    Product
    Hellas Meze Golden Smoked Whole Herring
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-2251-2026·2026-06-10

    BD Whitacre 22G spinal trays recalled in Huons bupivacaine sub-recall

    BD Spinal Trays with Whitacre needle 22 G, which contain bupivacaine with dextrose, are being recalled as a sub-recall of the Huons bupivacaine product recall. 330 units are affected.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405645.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0898-2026·2026-06-10

    Imported enoki mushrooms tested positive for Listeria monocytogenes in Florida

    Enoki mushrooms distributed by IQ Produce are being recalled after samples collected by the Florida Department of Health tested positive for Listeria monocytogenes.

    Product
    Enoki Mushroom, Net Weight 150g; Product of Korea; Distributed by IQ Produce UPC: 8809316 814286
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·H-0906-2026·2026-06-10

    Raw Shelled Peanuts Recalled for Undeclared Tree Nut Allergen

    Wilco Peanut Co is recalling raw shelled peanuts (Runner Type) because they may contain undeclared tree nuts, posing an allergen risk to consumers with nut allergies.

    Product
    Raw Shelled Peanuts (Runner Type) 2,200 lb. Poly Tote Bags and 50kg Poly Bags
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·H-0861-2026·2026-06-10

    Guittard cacao date sugar wafers recalled over potential Salmonella

    Guittard 72% Cacao Chocolate with Date Sugar Wafers in 25 lb cases are being recalled over potential contamination with Salmonella. 2,857 cases are affected.

    Product
    72% CACAO CHOCOLATE WITH DATE SUGAR WAFERS Ingredients: Cacao Beans, Organic Date Powder, Organic Cocoa Powder Net Wt 25lb (11.3kg) Made in the USA GUITTARD CHOCOLATE COMPANY Burlingame, CA 94010 Item: 0568C25 UPC: 00071818367654
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·H-0908-2026·2026-06-10

    Aramark cheese sauce contains dry milk powder recalled over Salmonella

    Aramark Cheese Sauce New & Improved in 25 lb bags is being recalled because it contains a dry milk powder ingredient recalled by the supplier over potential Salmonella contamination.

    Product
    Aramark Cheese Sauce New & Improved, 25 lb., packaged in a tied poly bag and packed 2 bags per case, UPC 0039954925121
    Category
    Food
    Distribution
    41 states
  • SevereFDA (Food)·H-0884-2026·2026-06-10

    Karlsburger garlic and cheese topper may contain Salmonella

    Karlsburger Kitchens Garlic N Cheese Topper in 20 oz jars is being recalled because the product may be potentially contaminated with Salmonella. 168 jars are affected.

    Product
    Karlsburger Kitchens Garlic N Cheese Topper, Net Wt: 20 oz. (567g). Distributed by: Karlsburger Foods, Inc., Monticello, MN 55362
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-2223-2026·2026-06-10

    Ivenix pump software may report false battery health and shut down

    The Ivenix Infusion System Large Volume Pump software is being recalled because a software anomaly can report a false battery-health value and trigger a shutdown alarm.

    Product
    LVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0887-2026·2026-06-10

    JCB Flavors sour cream and onion seasoning may contain Salmonella

    JCB Flavors Sour Cream & Onion seasoning in 10 lb bags is being recalled because the product may be potentially contaminated with Salmonella. Five cases are affected.

    Product
    #003020 Sour Cream & Onion, Net Wt: 10 lbs. JCB Flavors, 1224 Clark St. Watertown, WI 53094.
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·H-0903-2026·2026-06-10

    Birch Benders sweet potato pancake and waffle mix contains undeclared egg

    Birch Benders Sweet Potato Pancake and Waffle Mix, 12 oz, is being recalled because of undeclared egg. The recall covers 5,340 cases.

    Product
    Birch Benders Sweet Potato Pancake and Waffle Mix 12oz bag, UPC 8 1000156076 8, 6 bags per case
    Category
    Food
    Distribution
    20 states
  • HighFDA (Food)·H-0958-2026·2026-06-10

    Albertsons colossal Dubai cheesecake slice does not declare pistachio

    Albertsons store-made Cheesecake Slice Colossal Dubai is being recalled because the contains statement does not declare pistachio. 32 units are affected.

    Product
    UPC 25216200000 Cheesecake Slice Colossal Dubai. This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1022-2026·2026-06-10

    Albertsons fresh berry and chicken salad does not declare walnut

    Albertsons store-made Ready Meals Salad Fresh Berry & Chicken is being recalled because the contains statement does not declare walnut. 228 units are affected.

    Product
    UPC 21195200000 READY MEALS SALAD FRESH BERRY & CHICKEN SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0967-2026·2026-06-10

    Albertsons Dubai Boston creme cake does not declare pistachio

    Albertsons store-made Boston Creme Dubai 5-inch cake is being recalled because the contains statement does not declare pistachio. 25 units are affected.

    Product
    UPC 25814700000 CAKE BOSTON CREME DUBAI 5IN This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1028-2026·2026-06-10

    Albertsons assorted brownie platter does not declare walnut allergen

    Albertsons store-made Platter Brownies Assorted Seasonal is being recalled because the contains statement does not declare walnut. 15 units are affected.

    Product
    UPC 25511500000 PLATTER BROWNIES ASSORTED SEASONAL This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.
    Category
    Food
    Distribution
    Distributed nationwide