The Recall Desk

Severity 4 of 5

Severe recalls

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

851–875 of 32252

  • SevereFDA (Food)·H-0881-2026·2026-06-10

    JCB Flavors fiery hot seasoning may contain Salmonella

    JCB Flavors Fiery Hot Seasoning (Reduced Salt) in 25 lb bags is being recalled because the product may be potentially contaminated with Salmonella. 50 lbs are affected.

    Product
    #007560 Fiery Hot Seasoning (Reduced Salt), Net Wt: 25 lbs. JCB Flavors, 1224 Clark Street, Watertown, WI 53094
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-2278-2026·2026-06-10

    Design Options spinal trays recalled over Huons bupivacaine quality issues

    Design Options spinal needle anesthesia procedure kits are being recalled because they contain Bupivacaine Hydrochloride in Dextrose Injection subject to the Huons recall.

    Product
    Design Options Spinal Tray Spinal Needle Anesthesia procedure kits: Material Description (Material Number): SSK H M C 20061890 (560074), SSK S C H (560214), SSK BJC H S (ORIGINAL CUST) (560272), SSK CA P M C (ORIGINAL CUST) (560327), SSK T M H (560394), SSK S O 20070208…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2254-2026·2026-06-10

    BD Whitacre 25 gauge spinal trays recalled over bupivacaine quality issues

    BD Spinal Trays with a Whitacre 25 G needle, catalog number 405658, are being recalled as a sub-recall of the Huons bupivacaine product recall. 150 units affected.

    Product
    BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 2 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405658.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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
  • SevereNHTSA·26V376000·2026-06-09

    Ford Recalls Focus and Fusion Vehicles for Transmission Clutch Fracture Risk

    Ford is recalling 2015-2018 Focus and 2013-2016 Fusion vehicles previously repaired incorrectly under prior recalls. The clutch may fracture, causing transmission damage and fluid leaks that increase fire risk.

    Product
    FORD — FORD FOCUS, FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide