The Recall Desk

Hazard

Mis Labeling recalls

9,607 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,607
Critical
160
Severe
588
Most recent
2026-09-10

Of the 9,607 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.

4701–4725 of 9607

  • HighFDA (Food)·F-1956-2017·2017-05-03

    Pastry Foods Recalls Corn Sticks with Cheese for Undeclared Wheat

    Pastry Food Products Inc. is recalling 1 lb packages of Corn Sticks with Cheese because wheat is not declared on the ingredient list.

    Product
    Trigal Sorullos de Maiz con Queso (Corn Sticks with Cheese), Peso Neto (Net Weight) 1lb (454g), Manufacturado Por: Pastry Foods, Inc., Calle Elver #932, 1 Ext. Country Club, Rio Piedras, PR
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-2132-2017·2017-05-03

    Valley Bakery Almond Tea Ring Recalled for Undeclared Egg

    Valley Bakery Wholesalers Inc is recalling Almond Tea Rings because they contain egg but do not declare it on the label.

    Product
    Almond Tea Ring, Valley Bakery, Rock Valley, IA, 1 count. UPC 290401508001, packaged in clear plastic bags
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-2129-2017·2017-05-03

    Valley Bakery Apple Tea Ring Recalled for Undeclared Egg Allergen

    Valley Bakery Wholesalers Inc. is recalling Apple Tea Ring products because they contain egg but do not declare it on the label.

    Product
    Apple Tea Ring, Valley Bakery, Rock Valley, IA, 1 count. UPC 290400306006, packaged in clear plastic bags
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-2137-2017·2017-05-03

    Malgor Recalls Cedeira Octopus Tins Due to Mislabeling

    Malgor & Co. is recalling Cedeira Octopus in Oil Spiced Piquant tins because the label says octopus but the ingredients list jumbo squid.

    Product
    Cedeira Octopus in Oil Spiced Piquant, Net Weight 4.4oz (125g)
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-2143-2017·2017-05-03

    Econo Octopus Style Marinera Sauce Recalled for Squid Mislabeling

    Supermercado Econo Inc. is recalling Econo Octopus Style Marinera Sauce because the product contains squid but is labeled as octopus.

    Product
    Econo, Estilo Pulpo a la Marinera, Octopus Style Marinera Sauce, Net Wt. 4oz (115g)
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-2142-2017·2017-05-03

    Econo Octopus Style Product Recalled for Squid Mislabeling

    Supermercado Econo Inc. is recalling Econo Estilo Pulpo al Ajillo because the product contains squid but is labeled as octopus.

    Product
    Econo, Estilo Pulpo al Ajillo, Octopus Style with Garlic Flavor, Net Wt. 4oz (115g)
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1884-2017·2017-05-03

    XTANT Medical Recalls 5.5mm CoCr Straight Rods Due to Labeling Error

    XTANT Medical Inc. is recalling 97 units of 5.5mm CoCr Straight Rods because the labels may incorrectly identify the material as Ti6Al-4V ELI instead of Cobalt Chromium.

    Product
    5.5mm Diameter x 500mm CoCr Straight Rod, Model number X077-0420. The product is packaged in plastic bags with one piece per bag. Product Usage: The 5.5mm dia. X 500 mm CoCr Straight Rod is an accessory to the Fortex Pedicle Screw System. It is a straight rod connected betwe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1885-2017·2017-05-03

    Amendia Recalls Mislabeled Nitinol Guide Wires for Spinal Surgery

    Amendia is recalling 15 units of K-Wires labeled as stainless steel but made of nitinol. The wires were distributed to Georgia, Kansas, and Texas.

    Product
    01.4mm x 457mm (18in) K-Wire, Threaded Blunt, Ref 9080B-18T, Qty: 1 per pack, Material: SS 316L, Full Temper, per ASTM F138, Amendia, 1755 West Oak Parkway, Marietta, GA 30062 Guide Wires are used to establish a pathway into the bony pedicle to place implants during spinal s
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Food)·F-2094-2017·2017-04-26

    NuGo Slim Crunchy Peanut Butter Protein Bar Recalled for Undeclared Milk

    NuGo Nutrition is recalling specific lots of Slim Crunchy Peanut Butter Protein Bars because they were packaged in wrappers that do not list milk as an allergen.

    Product
    NuGo Slim Crunchy Peanut Butter Protein Bar, 5g net carbs, A gluten-free, soy protein bar with overall peanut butter and chocolate taste covered in dark chocolate, Best Buy 07/28/2017, manufactured for: NuGo Nutrition 520 second Street, Oakmont, PA 15139 INGREDIENTS: SLIM PROTE
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1871-2017·2017-04-26

    C.R. Bard Recalls SURESTEP Drainage Bags Due to Latex Mislabeling

    C.R. Bard is recalling 5,030 SURESTEP Drainage Bags because they are labeled as latex-free but may contain natural rubber latex.

    Product
    SURESTEP Tray, Bardex I.C. Complete Care Drainage Bag, 2000 ml Drainage Bag, 16 Fr., Sterile.
    Category
    Medical Device
    Distribution
    24 states
  • HighFDA (Food)·F-2082-2017·2017-04-26

    Sunshine Bakery Recalls Mixed Nut Mooncakes Due to Undeclared Sunflower Seeds

    Sunshine Bakery is recalling 280 units of Mixed Nut Mooncakes because the labels fail to declare sunflower seeds. The products were distributed to retail stores in California, Texas, and Nevada.

    Product
    MIXED NUT MOONCAKES (Trung Thu Thap Cam), individually packaged in clear wrap, with a printed label on top. Best by date is printed on the label. 5 oz/142 grams per unit with UPC code 015200401274
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1852-2017·2017-04-26

    Verathon Recalls GVL 2 Stat Blades Packaged with Incorrect Size

    Verathon is recalling GVL 2 Stat blades (lot GC32825) because they were physically packaged with the incorrect size device, GVL 1 Stat blades.

    Product
    It is recommended for patients with weight/size between 4-22 lbs (1.8-10 kg). Part Number 0270-0429: GVL 2 Stat (box of 10 Stats). Part Number 0574-0027: GVL 2 Stat (single pouched Stat). Part Number 0270-0662: GlideScope AVL Video Baton 1-2 Kit (where one box of 10, part nu
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1857-2017·2017-04-26

    Smith & Nephew Recalls D-RAD Locking Screws Due to Incorrect Expiration Dates

    Smith & Nephew is recalling 197 units of D-RAD locking screws because the expiration dates on the labels are incorrect and later than the actual expiration dates.

    Product
    D-RAD, S.T. LOCKING SCREWS, T7, QTY: (1), STERILE R, in the following sizes: (a) 2.4MM X 10MM, RES 74692410 (b) 2.4MM X 12MM, RES 74692412 (c) 2.4MM X 16MM, RES 74692416 (d) 2.4MM X 22MM, RES 74692422 (e) 2.4MM X 24MM, RES 74692424
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1835-2017·2017-04-26

    Ace Surgical Supply Recalls Incorrectly Packaged Dental Abutments

    Ace Surgical Supply Co., Inc. is recalling 87 INFINITY Internal Hex Healing Abutments because the incorrect device was packaged.

    Product
    INFINITY Internal Hex Healing Abutment, 4.5mm Platform, 4.7mm CW-3mm CH Straight; Product Code: 20145473 Product Usage: Non implantable dental abutment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1854-2017·2017-04-26

    Smith & Nephew Recalls Peri-Loc VLP Self-Tapping Cortex Screws Due to Labeling Error

    Smith & Nephew is recalling specific Peri-Loc VLP self-tapping cortex screws because the expiration dates printed on the labels are incorrect and later than the actual dates.

    Product
    Peri-Loc(R) VLP 3.5 MM X 6 MM SELF-TAPPING CORTEX SCREW, QTY: (1), STERILE R, REF 71801306 Orthopedic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1855-2017·2017-04-26

    Smith & Nephew Recalls D-RAD Locking Pegs Due to Incorrect Expiration Dates

    Smith & Nephew is recalling 19 units of D-RAD locking pegs because the expiration dates on the labels are incorrect and later than the actual dates.

    Product
    D-RAD, 1.8MM X 16MM, LOCKING PEG, QTY: (1), STERILE R, RES 74671816 Orthopedic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1856-2017·2017-04-26

    Smith & Nephew Recalls D-RAD Orthopedic Screws Due to Incorrect Expiration Dates

    Smith & Nephew is recalling 100 units of D-RAD orthopedic screws because the expiration dates on the labels are incorrect and later than the actual expiration dates.

    Product
    D-RAD, 2.4MMX 20MM, S.T. CORTEX SCREW, QTY: (1), STERILE R, RES 74682420 Orthopedic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1865-2017·2017-04-26

    Avid Medical Recalls Vacutainer Tubes Due to Mixed Component Lots

    Avid Medical is recalling 25,308 Vacutainer tubes because an expired component was found in a kit with a later expiration date, leading to incorrect lot and expiration labeling.

    Product
    Vacutainer Tubes Vacutainer tubes are intended for clinical laboratory hematology studies including but not limited to lead level testing, FEP level testing, and CBC testing.
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·17V273000·2017-04-25

    Ram ProMaster Recall for Incorrect Air Bag Labeling

    Chrysler is recalling 2014-2017 Ram ProMaster vehicles because labels incorrectly state they have frontal air bags. This mislabeling may increase injury risk in a crash.

    Product
    RAM — RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1958-2017·2017-04-19

    Dolcetta White Chocolate Coconut Snowman Recalled for Undeclared Soy and Milk

    Dolcetta Artisan Sweets is recalling White Chocolate Coconut Snowman products due to undeclared soy lecithin and milk allergens.

    Product
    White Chocolate Coconut Snowman. White chocolate with coconut shaped like a snowman, net wt. 45g (1.6 oz). Product packaged in clear plastic bag with a twist tie closure. The label declared "***White Chocolate Coconut Snowman***34% white chocolate, coconut, coconut milk powd
    Category
    Food
    Distribution
    2 states