The Recall Desk

Hazard

Mis Labeling recalls

9,606 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,606
Critical
160
Severe
588
Most recent
2026-09-09

Of the 9,606 mis labeling recalls we have scored against our rubric, 160 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 588 (6%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all mis labeling recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

476–500 of 9606

  • SevereFDA (Food)·F-1224-2024·2024-05-15

    D-LO's Pistachio Cheesecake Recalled for Undeclared Allergens and Food Coloring

    D-LO's Delightful Gourmet Cheesecake in pistachio flavor is being recalled due to undeclared wheat and soy allergens and undeclared food colors. The product poses a health risk to consumers with allergies to these ingredients.

    Product
    D-LO's Delightful Gourmet Cheesecake, Pistachio, 142g single serve UPC 8 60007 40398 9, and 678g six serving UPC 8 60007 40395 8, both serving sizes in clear plastic container with hinged lid
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1219-2024·2024-05-15

    FDA Recalls Sacramento Cookie Factory Wine Wafers for Undeclared Milk Allergen

    Sacramento Cookie Factory recalls Original Wine Wafer - Lemon Vanilla cookies in multiple states due to undeclared milk allergen. Consumers with milk allergies should not consume this product.

    Product
    Original Wine Wafer - Lemon Vanilla [Two sizes: retail package of 8 wafers (7 oz) and retail gift package of 2 wafers (2 oz)]
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-1785-2024·2024-05-15

    Stryker Dynamic Mesh Mislabeled with Incorrect Catalog Number

    Stryker shipped 63 units of cranial mesh labeled as catalog 56-90614 (Gold) but actually containing 56-90314 (Blue) mesh. The mislabeling may cause procedural delays.

    Product
    Stryker 1,5/1,7MM DYNAMIC MESH- STD-MEDIUM-Intended for the reconstruction, stabilization and rigid fixation of the bony areas of the cranial skeleton. Catalog Number: 56-90614
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V333000·2024-05-14

    Mack MD and Terrapro trucks recalled for incorrect weight rating

    Mack is recalling certain 2024-2025 MD and Terrapro vehicles because the Gross Axle Weight Rating (GAWR) on the certification label is incorrect, allowing vehicles to be overloaded and increasing crash risk. Dealers will replace the label free of charge.

    Product
    MACK — MACK TERRAPRO (TE), MD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V327000·2024-05-10

    2024-2025 BMW X5 Tire Placard May Display Incorrect Size and Pressure

    BMW is recalling certain 2024-2025 X5 xDrive40i models because the tire information placard may display incorrect tire size and pressure, potentially leading to improper tire installation or inflation and increased crash risk.

    Product
    BMW — BMW X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1245-2024·2024-05-08

    International Bread Pita Chips Recalled for Undeclared Wheat Allergen

    International Bread Pita Chips are being recalled because the product label lists flour as an ingredient but fails to disclose that wheat is a sub-ingredient of the flour, a major allergen.

    Product
    International Bread Pita Chips Retail Clamshell Container: 10oz., Bulk bag: 10lbs. Garlic Baked Pita Chips: 6 81942 22111 3
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1211-2024·2024-05-08

    Johnny's Parmesan Garlic Seasoning recalled for undeclared sesame allergen

    Johnny's Parmesan Garlic Seasoning contains undeclared sesame seeds that are visible through the bottle but not listed on the label. The product may pose a risk to consumers with sesame allergies.

    Product
    Bottle is labeled as Johnny's Parmesan Garlic Seasoning, 5oz (141g), packaged in poly bottle with green spice cap, UPC 0 70381 10060 6. Distributed by Johnny s Fine Foods Inc. 319 E. 25th St. Tacoma, WA 98421. Label declares: CONTAINS: MILK. MANUFACTURED IN A FACILITY THAT ALSO
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-1244-2024·2024-05-08

    International Bread Pita Chips Recalled for Undeclared Wheat Allergen

    International Bread Pita Chips are recalled because the label declares flour as an ingredient but does not identify wheat as a sub-ingredient. This poses a risk to consumers with wheat allergies.

    Product
    International Bread Pita Chips Retail Clamshell Container: 10oz., Bulk bag: 10lbs. UPC: Plain Baked Pita Chips: 6 81942 22110 6
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0481-2024·2024-05-08

    Prescription Valacyclovir Tablets Recalled Due to Missing Imprint

    Viatris Inc is recalling 143,230 bottles of Valacyclovir Hydrochloride 500 mg tablets due to missing imprints on some tablets. The recall is nationwide and affects two lot numbers expiring in June 2024 and May 2025.

    Product
    VALACYCLOVIR HYDROCHLORIDE — VALACYCLOVIR HYDROCHLORIDE (VALACYCLOVIR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0480-2024·2024-05-08

    Fentanyl Injection Bags Recalled Due to Incorrect Barcode Labels

    Hikma Injectables USA Inc. has recalled 1,895 bags of Fentanyl 1000mcg/100mL injection (lot CH0324001) due to incorrect barcodes on the product labeling.

    Product
    Fentanyl 1000mcg/100mL (10mcg/mL) in 0.9% Sodium Chloride Injection, packaged in 100mL bags, Rx only, Compounded by: Hikma Injectables USA Inc. 2 Esterbrook Lane, Cherry Hill, NJ 08003, Distributed by: Hikma Injectables USA Inc. 36 Stults Road, Dayton, NJ 08810, NDC 63037-100-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateNHTSA·24V315000·2024-05-03

    Heartland Recalls 2024 Eddie Bauer Travel Trailers for Incorrect Tire Placards

    Heartland is recalling 2024 Eddie Bauer travel trailers because tire placards list the wrong tire size. This labeling error could lead to incorrect tire installation and increased crash risk.

    Product
    HEARTLAND — HEARTLAND EDDIE BAUER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1204-2024·2024-05-01

    Roly Poly Bakery Multigrain Bread Recalled for Undeclared Egg

    Roly Poly Bakery is recalling multigrain bread sold in Connecticut and Massachusetts because it contains undeclared egg, a major food allergen. Consumers with egg allergies should not consume this product.

    Product
    Roly Poly Bakery brand MULTIGRAIN bread; INGREDIENTS: Whole Wheat Flour, High Gluten Flour, Ryechops, Sesame, Caraway, Brownflex, Soybean, Pearl Wheat, Sunflower, Salt, Water.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0449-2024·2024-05-01

    Honey product recalled nationwide for undeclared sildenafil and tadalafil

    Pyramids Wholesale Inc. is recalling Weiner Boner Honey due to undeclared sildenafil and tadalafil. The product was distributed nationwide without FDA approval.

    Product
    Weiner Boner Honey, 12g packet, 100% Organic Formula.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1635-2024·2024-05-01

    Palindrome Precision H Chronic Catheter Kit may lack labeled heparin coating

    Covidien is recalling 878 units of Palindrome Precision H Chronic Catheter Kits that may lack the heparin anticoagulant coating indicated on the label, potentially reducing clot prevention during hemodialysis.

    Product
    Palindrome Precision H Chronic Catheter Kit 14.5 Fr/Ch (4.8mm) x 23 cm (Symmetrical Tip, Heparin Coating and Tal VenaTrac Stylet- Intended for acute and chronic hemodialysis, apheresis, and infusion. Model Number (CFN): 8888145044CP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1203-2024·2024-05-01

    PepsiCo Root Beer Mislabeled; Regular Mug Sold as Zero Sugar

    PepsiCo is recalling 2,801 cases of 12-pack Mug root beer that were mislabeled as Mug Zero Sugar but contain regular Mug. The error affects product distributed across six states.

    Product
    12 oz Aluminum cans of root beer packaged 12 cans per carton. 2/12pks per case
    Category
    Food
    Distribution
    6 states
  • CriticalUSDA FSIS·015-2024·2024-04-26

    802 VT Frozen Recalls Meat Pizza for Undeclared Soy Allergen

    802 VT Frozen is recalling approximately 8,221 pounds of frozen meat pizza because the product contains soy, a known allergen, that is not declared on the label.

    Product
    VT Pie and Pasta Co. — 802 VT Frozen Recalls Frozen Meat Pizza Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-1522-2024·2024-04-24

    Marketing brochures for Baxter surgical vessel occluders contain inaccurate information

    Baxter Healthcare is recalling marketing brochures for surgical vessel occluders and related devices because the brochures contain information that does not match the official product instructions for use.

    Product
    Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-210004 Surgical Tools Website v1, and US-AS46-230002 CV Specialty Brochure US version which affect: Flo-Rester Disposable Internal Vessel O
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1523-2024·2024-04-24

    Surgical and Cardiovascular Device Marketing Brochures Recalled for Documentation Errors

    Baxter Healthcare is recalling surgical and cardiovascular device marketing brochures that contain information conflicting with the official Instructions for Use. The inaccurate content could lead to incorrect device use.

    Product
    Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-210004 Surgical Tools Website v1, and US-AS46-230002 CV Specialty Brochure US version which affect: Flo-Thru Intraluminal Shunt, Item Numbe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1524-2024·2024-04-24

    Baxter surgical tool marketing brochures contain inaccurate Instructions for Use

    Baxter Healthcare Corporation recalled marketing brochures for surgical tools that contain inaccurate information conflicting with the product Instructions for Use. Over 82,000 units were distributed worldwide.

    Product
    Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-210004 Surgical Tools Website v1, and US-AS46-230002 CV Specialty Brochure US version which affect: Vascular Probe, Item Numbers: a) 708101
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1153-2024·2024-04-24

    Aromitalia Malasia Coconut Paste Recalled for Missing Coconut Allergen in Contains Statement

    Aromitalia Malasia Coconut Paste is being recalled because coconut is listed in the ingredients but not declared in the contains statement, potentially affecting consumers with coconut allergies.

    Product
    Aromitalia Malasia Coconut Paste + 35.27 oz milk-based mix, Net Weight 123.46 oz, plastic container.
    Category
    Food
    Distribution
    7 states
  • CriticalFDA (Food)·F-1140-2024·2024-04-17

    Robeson Enterprises Mo' Money Pie Recalled for Undeclared Soy Allergen

    Robeson Enterprises is recalling Mo' Money Pie due to undeclared soy allergen on the label. The product was distributed to Georgia, North Carolina, and South Carolina.

    Product
    PIES & SIDES MO' MONEY PIE INGREDIENTS: BLACK EYED PEAS, COLLARDS, ELBOW PASTA, CHEESES, CORNMEAL, BLEACHED FLOUR, MILK PRODUCTS, SPICES. CONTAINS: MILK, EGG, WHEAT PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1136-2024·2024-04-17

    Deep South Tomato Pie Recalled for Undeclared Eggs

    Robeson Enterprises is recalling Deep South Tomato Pie because the label does not list sub-ingredients, and pimento cheese in the product may contain undeclared eggs. Consumers with egg allergies should not consume this product.

    Product
    PIES & SIDES DEEP SOUTH TOMATO PIE, INGREDIENTS: SLICED TOMATOES, PIMENTO CHEESE, BLEACHED FOUR, MILK PRODUCTS, SPICES. CONTAINS: SOY, FISH, WHEAT, MILK PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1133-2024·2024-04-17

    PIES & SIDES Broccoli Casserole Recalled for Missing Ingredient Labels

    PIES & SIDES Broccoli Casserole by Robeson Enterprises is recalled because the product label does not list ingredients. The product contains wheat, eggs, milk, soy, and fish.

    Product
    PIES & SIDES Broccoli Casserole Contains: Wheat, Eggs, Milk, Soy, Fish PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1132-2024·2024-04-17

    Egg Salad Sandwich Recalled for Undeclared Fish Allergen Mislabeling

    Tuna salad sandwiches were mislabeled as egg salad, creating an undeclared fish allergen risk for consumers. The recall affects 551 units distributed to institutions and retailers across ten states.

    Product
    Egg salad sandwich packaged in clamshell for individual sale. 7.22oz (205g) UPC 766375938415
    Category
    Food
    Distribution
    10 states