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.

9526–9550 of 9622

  • ModerateFDA (Devices)·Z-1819-2012·2012-06-27

    NIMS Recalls Exer-Rest Brochures for Unsubstantiated Claims

    Non-Invasive Monitoring Systems is voluntarily recalling 3,665 Exer-Rest marketing brochures nationwide because they contain unsubstantiated health claims.

    Product
    US-001 Rev A brochure is a two sided tri-fold printed marketing brochure describing the approved labeling indications for use, precautions and general operational information of the Exer-Rest device, Models AT3800 and AT4700. Ever-Rest US Brochure US-001 Rev A. Brochure:
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1820-2012·2012-06-27

    NIMS Recalls Exer-Rest Brochures for Unsubstantiated Claims

    Non-Invasive Monitoring Systems, Inc. is voluntarily recalling 91 Exer-Rest marketing brochures nationwide because they contain unsubstantiated health claims.

    Product
    USA-002 Rev A brochure is a two sided tri-fold printed marketing brochure describing the approved labeling indications for use, precautions and general operational information of the Exer-Rest device, Models AT3800 and AT4700. Brochure: "EXER-REST***A patented, FDA regist
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1420-2012·2012-06-20

    Cheese Coffee Cake Recalled for Undeclared Milk Allergen

    Super Mom's is recalling Country Fresh Ovens Cheese Coffee Cake because label audits found an undeclared milk allergen.

    Product
    Country Fresh Ovens Cheese Coffee Cake, Net Wt 5 oz (142g). Dist. by Country Fresh Ovens, St. Paul Park, MN 55071
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1405-2012·2012-06-20

    Bear Paws Pastry Recalled for Undeclared Wheat Allergen

    JDS Bakery LLC is recalling Bear Paws Microwaveable Pastry because the labels do not declare wheat, a major food allergen.

    Product
    Bear Paws MICROWAVEABLE A Pastry Ingredients: Flour (unbleached), powdered sugar, sugar, walnuts, water, vegetable shortening Net Wt 8oz Stahl's Bakery (586) 716-8500
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1389-2012·2012-06-20

    Best West Foods Recalls Cheese Lasagna Rolls Due to Missing Soy Labeling

    Best West Foods is recalling Cheese Lasagna Rolls because soy was not listed in the ingredient statement or allergen information on the label.

    Product
    Cheese Lasagna Rolls; Perishable, keep frozen; Net weight 15 pounds, 60 x 4 oz. For HRI Use Only. Cook Thoroughly per state food code standards. West Best Foods, inc. 3425 Wynn Road, Las Vegas, NV 89102
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1404-2012·2012-06-20

    JDS Bakery Recalls Cinnamon Rolls Due to Undeclared Wheat Allergen

    JDS Bakery LLC is recalling 60 packages of Cinnamon Rolls A Pastry because the labels fail to declare wheat as an ingredient.

    Product
    Cinnamon Rolls A Pastry Ingredients: Spring Flour (unbleached), water, powdered sugar sugar, vegetable shortening Net Wt 8oz Stahl's Bakery (586) 716-8500
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1403-2012·2012-06-20

    JDS Bakery Recalls White Brick Oven Bread Due to Undeclared Wheat

    JDS Bakery LLC is recalling 300 packages of White Brick Oven White Bread because the labels fail to declare wheat sub-ingredients.

    Product
    White brick oven WHITE BREAD INGREDIENTS: Spring Flour (unbleached), water vegetable shortning... Stahl's Bakery (586) 716-8500
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1388-2012·2012-06-20

    Best West Foods Recalls Lasagna Rolls Due to Undeclared Soy

    Best West Foods is recalling Cheese and Florentine Lasagna Rolls because soy was not listed on the label. The product was distributed in Nevada.

    Product
    Florentine Lasagna Rolls; Perishable, keep frozen; Net weight 15 pounds, 60 x 4 oz. For HRI Use Only. Cook Thoroughly per state food code standards. West Best Foods, inc. 3425 Wynn Road, Las Vegas, NV 89102
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1807-2012·2012-06-20

    Vygon Recalls Heparin Lock Flush Syringes and Dressing Change Kits

    Vygon Corporation is voluntarily recalling Heparin Lock Flush Syringes and kits containing them due to a related recall of VY Flush Heparin Lock Flush Syringes.

    Product
    Churchill Medical Systems, Inc. DRESSING CHANGE KIT Prefilled syringes included in the kit are used to maintain the patency of indwelling catheter lumens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1808-2012·2012-06-20

    Vygon Recalls Heparin Lock Flush Syringes and PICC Insertion Kits

    Vygon is recalling Heparin Lock Flush Syringes and kits containing them due to a voluntary recall of similar syringes by the manufacturer.

    Product
    Churchill Medical Systems, Inc. A VYGON COMPANY PICC INSERTION TRAY Prefilled syringes included in the kit are used to maintain the patency of indwelling catheter lumens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1402-2012·2012-06-20

    Stahl's Famous Original Bakery Cutout Cookies Recalled for Undeclared Ingredients

    JDS Bakery LLC is recalling 80 packages of 14-oz Stahl's Famous Original Bakery Cutout Cookies because the labels fail to declare specific sub-ingredients.

    Product
    Stahl's Famous Original Bakery CUTOUT COOKIES 14oz. INGREDIENTS: Pastry Flour, Sugar, Shortening...Contains Wheat, Eggs, Milk and Soy.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1401-2012·2012-06-20

    Panera Cream Cheese Spread Recalled for Ingredient Labeling Error

    Panera Bread LLC is recalling Reduced Fat Hazelnut Cream Cheese Spread because the ingredient statement on the label was reversed. The product name on the label is correct.

    Product
    Panera ,HAZELNUT CREAM CHEESE SPREAD Reduced Fat, 8 0z , Refrigerated
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1803-2012·2012-06-20

    Vygon Recalls Heparin Lock Flush Syringes and Kits

    Vygon Corporation is voluntarily recalling Heparin Lock Flush Syringes and kits containing them due to a related recall of VY Flush Heparin Lock Flush Syringes.

    Product
    Churchill Medical Systems, Inc. PORT-A-CATH Tray Kit Prefilled syringes included in the kit are used to maintain the patency of indwelling catheter lumens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1805-2012·2012-06-20

    Vygon Recalls Heparin Lock Flush Syringes and Kits

    Vygon Corporation is recalling Heparin Lock Flush Syringes and kits due to a voluntary recall of related VY Flush Heparin Lock Flush Syringes.

    Product
    Churchill Medical Systems, Inc. VAD ACCESS TRAY Kit Prefilled syringes included in the kit are used to maintain the patency of indwelling catheter lumens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1381-2012·2012-06-20

    Endo Pharmaceuticals Recalls Endocet Tablets Due to Foreign Tablet Contamination

    Endo Pharmaceuticals is recalling specific bottles of Endocet 10 mg/650 mg tablets because some contained mixed 10 mg/325 mg tablets.

    Product
    Endocet (oxycodone and acetaminophen) tablets, USP, 10 mg/650 mg, 100-count tablets per bottle, Rx only, Manufactured for: Endo Pharmaceuticals Inc., Chadds Ford, PA, By: Novartis, Lincoln, NE 68501; NDC 60951-797-70.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1795-2012·2012-06-20

    Integra Mozaik Strip Recalled for Incorrect Instructions for Use Translation

    Integra LifeSciences Corp. is recalling Integra Mozaik Strip units because the Instructions for Use contain incorrect Spanish and French translations of the term "bone marrow aspirate."

    Product
    Integra Mozaik Strip 10 cc Product Usage: The product is a bone graft substitute composed of collagen (Type 1) and ceramic (I3-Tricalcium phosphate) matrix in putty and strip forms. The product is intended for use as a bone void filler to fill voids or gaps of the skeletal
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-1796-2012·2012-06-20

    Integra Mozaik Putty Recalled for Incorrect Instructions for Use Translation

    Integra LifeSciences Corp. is recalling 42 units of Mozaik Putty because the Instructions for Use contain incorrect Spanish and French translations of the term 'bone marrow aspirate'.

    Product
    Integra Mozaik Putty 2.5cc, 5 cc, 10 cc Product Usage: The product is a bone graft substitute composed of collagen (Type 1) and ceramic (IP3-Tricalcium phosphate) matrix in putty and strip forms. The product is intended for use as a bone void filler to fill voids or gaps
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·12V255000·2012-06-05

    Toyota Recalls 2013 Scion FR-S for Inaccurate Owner's Manual Air Bag Info

    Toyota is recalling 2013 Scion FR-S vehicles because the owner's manual contains inaccurate descriptions of the front passenger air bag system, which could increase injury risk in a crash.

    Product
    SCION — SCION FR-S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·12V254000·2012-06-05

    Subaru Recalls 2013 BRZ Vehicles for Inaccurate Owner's Manual Information

    Subaru is recalling 1,886 model year 2013 BRZ vehicles because the owner's manual contains inaccurate descriptions of the front passenger occupant classification and air bag systems.

    Product
    SUBARU — SUBARU BRZ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12V183000·2012-04-27

    Jayco Recalls 2012 Jay Flight Trailers for Incorrect Tire Labels

    Jayco is recalling certain 2012 Jay Flight Bungalow travel trailers because incorrect tire labels could lead to improper inflation or loading, increasing crash risk.

    Product
    JAYCO — JAYCO JAY FLIGHT
    Category
    Vehicle
    Distribution
    Distributed nationwide