The Recall Desk

Hazard

Mis Labeling recalls

9,622 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,622
Critical
163
Severe
590
Most recent
2026-09-24

Of the 9,622 mis labeling recalls we have scored against our rubric, 163 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 590 (6%) are Severe.

Which agencies issued them

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.

9476–9500 of 9622

  • LowFDA (Devices)·Z-1990-2012·2012-07-18

    PSC Industries Recalls Button Switch Pen Electrodes Due to Labeling Errors

    PSC Industries is recalling 50 units of Button Switch Pen Electrodes due to a labeling error where the manufacturer symbol replaced the expiration date symbol.

    Product
    Button Switchpens, w/Extendable Needle Electrode 2 mm Exposure Single Use Electrosurgical./Extendable Pencils, 510(k) #K936304, Model Number: 75820. The device is packaged in a sterile Tyvek peel pouch within a cardboard box which contains 24 pouches per box. Pens/Pencils an
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1996-2012·2012-07-18

    PSC Industries Recalls Bayonet Forceps Due to Incorrect Expiration Date

    PSC Industries is recalling 80 units of Bayonet Forceps because the outer carton lists an incorrect sterile expiration date, though the individual pouch labels are correct.

    Product
    Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Insulated Tips, Sterile Single Use Surgical/Bipolar Forceps, Model #20-1360I, 510 (k) #K884656. The surgical device is package one (s) per plastic Tyvek peel pouch, 10 plastic Tyvek peel pouches per box. Bipolar Forceps and Cords - Ol
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1991-2012·2012-07-18

    PSC Industries Recalls Button Switchpens Due to Labeling Errors

    PSC Industries is recalling Button Switchpens because the packaging labels incorrectly state the devices include a holster. The recall covers 725 units distributed nationwide.

    Product
    Button Switchpens, w/Extendable Needle Electrode 10 mm Exposure, Single Use device, Electrosurgical./Extendable Pencils, 510(k)#K936304, Model Number: 75800. The device is packaged in a sterile Tyvek peel pouch within a cardboard box. The cartons contain 25 pouches per box.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1691-2012·2012-07-11

    Mexicantown Wholesale Recalls Muffins with Pecans for Undeclared Soy Allergen

    Mexicantown Wholesale is recalling specific muffin products containing pecans due to undeclared soy ingredients. The recall affects products distributed in Canada.

    Product
    Muffins with Pecans: 1) MUFFIN W/PECANS (MEXICAN BREAD) IMPORTED BY EL CAMPEON LEAMINGTON 519-324-2616 4oz; UPC 9564000029, item #002; 2) MUFFIN W/PECANS MEXICAN SWEET BREAD IMPORTED BY MAX PRODUCTS LEAMINTON 519-325-1176 MEXICANTOWN BAKERY DETROIT MI 48210 4.0oz, UPC 9564000029;
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1708-2012·2012-07-11

    Ultradent Recalls Cinnamon Xylishield Gum Due to Missing Soy Allergen Labeling

    Ultradent is recalling 36 lots of Cinnamon Xylishield gum because the packaging fails to list soy as an ingredient. The gum was distributed globally.

    Product
    Cinnamon Xylishield xylitol gum, net wt 84 g, Ultradent Products, South jordan, UT 84095 60 pieces of gum per pack. Packaging is red, white, and black with black, red and white print writing. The product is advertised for use in fighting against tooth decay. Part number 8419.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1709-2012·2012-07-11

    Ultradent Recalls Cinnamon Xylishield Gum Due to Missing Soy Allergen Labeling

    Ultradent is recalling 36 lots of cinnamon Xylishield gum because the ingredients label failed to list soy, a major allergen.

    Product
    Xylishield Dental Care Kit containing 60 pieces of Cinnamon Xylishield gum. The product is packaged in blue and white packaging with black and white print writing. The product is advertised as a defense against cavities. Part number 8405.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1711-2012·2012-07-11

    Cedar's Bakery White Pita Bread Recalled for Wheat Allergen Mislabeling

    Cedar's Bakery is recalling White Pita Bread because the wheat flour ingredient is not labeled as an allergen.

    Product
    Cedar's Bakery Pita Bread, 10 loaves, White; ingredients flour water,yeast, sugar, salt. Nt. Wt. 22 oz.(1 lb. 6 oz. - 624 GMs)
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1710-2012·2012-07-11

    Ultradent Recalls Xylishield Gum for Missing Soy Allergen Labeling

    Ultradent is recalling specific lots of Xylishield gum because the packaging failed to list soy as an ingredient. A separate lot of spearmint gum was also recalled due to accidental cinnamon flavoring.

    Product
    Spearmint Xylishield xylitol gum, net wt 84 g, Ultradent Products, South jordan, UT 84095 60 pieces of gum per pack. Packaging is aqua, blue and white with black, aqua and white print writing. The product is advertised for use in fighting against tooth decay. Part number 8418.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1701-2012·2012-07-11

    Mexican Sweet Bread Recalled for Undeclared Yellow 6

    Mexicantown Wholesale is recalling 26 units of Empanadas de Pina (Mexican Sweet Bread) due to undeclared Yellow 6.

    Product
    1) EMPANADAS DE PINA (MEXICAN SWEET BREAD) IMPORTED BY EL CHARRO MEXICANTOWN BAKERY DETROIT MI 48210 3.4oz 21-MAY-12, UPC: 9564000009 2) EMPANADAS DE PINA (MEXICAN SWEET BREAD/pain sucre) IMPORTED BY FIESTA WHOLESALE 226-440-3033 MY LITTLE MEXICO 3.4oz
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-1712-2012·2012-07-11

    Rosati Watermelon Water Ice Recalled for Undeclared Yellow Dye

    SR Rosati, Inc. is recalling Rosati Cry Baby Sour Watermelon water ice because the label does not declare FD&C Yellow #5.

    Product
    Rosati Cry Baby Sour Watermelon water ice, 6 fl oz
    Category
    Food
    Distribution
    7 states
  • LowFDA (Drugs)·D-1399-2012·2012-07-11

    Watson Loxapine Capsules Recalled for Outdated Patient Outsert

    Watson Laboratories is recalling 8,254 bottles of Loxapine Capsules 5mg because an outdated patient outsert was used during packaging.

    Product
    Loxapine Capsules USP, 5mg, 100 count bottle, Rx only Manufactured By: Watson Laboratories Inc., Corona, CA 92880 NDC # 00591-0369-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1406-2012·2012-07-11

    Health Plus Super Colon Cleanse Recalled for Labeling Error

    Health Plus Incorporated is recalling Super Colon Cleanse capsules because the Drug Facts label incorrectly describes the active ingredient per dose instead of per capsule.

    Product
    Super Colon Cleanse, stimulant laxative, 140 mg of Senna per capsule, 25 doses, 100 capsules, Manufactured by: healthPLUS Inc. Chino, CA 91710 USA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1403-2012·2012-07-11

    Watson Recalls Loxapine Succinate Capsules Due to Outdated Patient Outsert

    Watson Laboratories is recalling 7,262 bottles of Loxapine Succinate Capsules because an outdated patient outsert was used during packaging.

    Product
    Loxitane Capsules, Loxapine Succinate Capsules, 10mg base, 100 count bottle, Rx only, Watson Laboratories Inc., Corona, CA 92880 NDC # 52544-495-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1402-2012·2012-07-11

    Watson Recalls Loxapine Capsules Due to Outdated Patient Outsert

    Watson Laboratories is recalling 18,902 bottles of Loxapine 50mg capsules because an outdated patient outsert was used during packaging.

    Product
    LOXAPINE — LOXAPINE (LOXAPINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1654-2012·2012-07-04

    PGP International Recalls iForce Nutrition Protein Powder for Undeclared Wheat

    PGP International is recalling iForce Nutrition PROTEAN Lean Protein powder because it contains undeclared wheat. The product was distributed in California, North Carolina, and Wisconsin.

    Product
    iForce Nutrition Xtreme Series, PROTEAN, Lean Protein, Strawberry Creamsicle, Dietary Supplement, 4 lbs. Mfg. for Dist by, Tribravus Enterprises, LLC, Vista, CA 92081
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1677-2012·2012-07-04

    Crispy Pistachio Cookies Recalled for Undeclared Milk and Almond

    Indian Foods & Spices, LLC is recalling Crispy by TWI Foods Pistachio Cookies because they may contain undeclared milk and almond.

    Product
    Crispy by TWI Foods Pistachio Cookies, Biscuit, Net Wt 400 g, Product of Canada Manufactured by TWI Foods Inc. 2600 Drew Road, Mississauga, Ont, Canada L4T3M5.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1868-2012·2012-07-04

    MedComp 8F Plastic Pro-Fuse CT Low Profile Port Recall

    Medical Components, Inc. is recalling 30 kits of the MedComp 8F Plastic Pro-Fuse CT Low Profile Port because the kits contain the wrong port model.

    Product
    MRCTT80041 MedComp 8F Plastic Pro-Fuse(R) CT Low Profile Port with Attachable Chronoflex(R) Polyurethane Catheter. Power Injectable Implantable Infusion Port insertion kit.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1636-2012·2012-07-04

    Young Ocean Recalls Salted Pollock Roe Due to Undeclared Artificial Colors

    Young Ocean, Inc. is recalling approximately 1,920 pounds of salted pollock roe sold in Washington due to the use of undeclared artificial colors Red #5, Yellow #5, and Red #40.

    Product
    Salted/marinated Pollock roe packaged in white plastic trays with either a clear or opaque plastic lid. Product is packaged in 1.0 lb., 2.2 lb., and 5 lb. sizes and is labeled in part: "Marinated Pollock Roe***Weight: 5.0lb***Production Date: March 2012 Packed by: Young Ocean In
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1666-2012·2012-07-04

    Mexicantown Wholesale Recalls Tacos de Pina for Undeclared Dye

    Mexicantown Wholesale is voluntarily recalling Tacos de Pina due to undeclared FD&C Yellow #5. The recall affects 11 products distributed in Michigan.

    Product
    TACOS DE PINA QTY: 120 MEXICANTOWN BAKERY 313-894-2000
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1895-2012·2012-07-04

    Zimmer Recalls Shoulder Surgery Drill Due to Labeling Error

    Zimmer, Inc. is recalling 87 units of a shoulder surgery drill because the catalog number on the packaging did not match the actual product.

    Product
    Bigliani/Flatow The Complete Shoulder Solution Trabecular Metal Glenoid Instrument Drill with Stop, 6 mm; the products are medical instruments intended for use when performing surgery of the shoulder.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1659-2012·2012-07-04

    Mexicantown Wholesale Recalls Concha Chocolate for Undeclared Dye

    Mexicantown Wholesale is voluntarily recalling Concha Chocolate products due to the presence of undeclared FD&C Yellow #6.

    Product
    CONCHA CHOCOLATE QTY: 90 MEXICANTOWN BAKERY 313-894-2000
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1661-2012·2012-07-04

    Mexicantown Wholesale Recalls Concha Rosa for Undeclared Yellow Dye

    Mexicantown Wholesale is voluntarily recalling Concha Rosa products distributed in Michigan due to the presence of undeclared FD&C Yellow #6.

    Product
    CONCHA ROSA QTY: 90 MEXICANTOWN BAKERY 313-894-2000
    Category
    Food
    Distribution
    1 state