The Recall Desk

Hazard

Mis Labeling recalls

9,610 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,610
Critical
161
Severe
588
Most recent
2026-09-16

Of the 9,610 mis labeling recalls we have scored against our rubric, 161 (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.

6176–6200 of 9610

  • ModerateNHTSA·15V571000·2015-09-11

    Land Rover Recalls 2014 Range Rover Sport for Air Bag Handbook Error

    Jaguar Land Rover is recalling 5,914 vehicles because the owner's handbook incorrectly describes the Air Bag Status Indicator Lamp, potentially increasing injury risk in a crash.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3074-2015·2015-09-09

    Kilwin's Recalls Sugar Free Milk Chocolate Caramels Due to Undeclared Cashew

    Kilwin's is recalling 5-ounce containers of Sugar Free Milk Chocolate Caramels because they may contain undeclared cashew, posing a risk to those with allergies.

    Product
    5 ounce containers of SUGAR FREE Milk Chocolate Caramels. The 5 oz container is a cardboard box with clear plastic window on the front. Retail packages are packed 4 per shipping case.
    Category
    Food
    Distribution
    12 states
  • ModerateFDA (Food)·F-3075-2015·2015-09-09

    think Thin Oatmeal Recalled for Incorrect Honey Peanut Butter Labeling

    Interpac Technologies is recalling think Thin oatmeal cups that have the correct lid but an incorrect Honey Peanut Butter label. The product contains visible nuts.

    Product
    think Thin Protein & Fiber Oatmeal, Madagascar Vanilla, Almonds, Pecans; 10 g Protein, 5 g Fiber, 190 calories; Net wt 1.76 oz. (50g); (Nuts are visible in product when lid is opened. Tray - 12 x 1.76 oz cups UPC 753656711881: Individual cup UPC 753656 711874 Ingredients:
    Category
    Food
    Distribution
    16 states
  • ModerateFDA (Devices)·Z-2486-2015·2015-09-09

    FDA Recalls Bright Embrace Bili Light Due to Incorrect Temperature Labeling

    Physician Engineered Products, Inc. is recalling 97 Bright Embrace Single Bili Lights because the upper limit for ambient temperature was printed incorrectly in the instructions.

    Product
    Bright Embrace, a Single Bili Light for newborn phototherapy Distributed by: Physician Engineered Products, Inc., Model SBL60
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Food)·F-3077-2015·2015-09-09

    Big Train Vanilla Chai Tea Mix Recalled for Mislabeling Sugar Content

    Big Train Inc. is recalling one lot of Vanilla Chai Tea Latte mix because it is labeled 'No Sugar Added' but actually contains sugar.

    Product
    Big Train Chai Tea Vanilla Chai, Naturally and Artificially Flavored Drink Mix, No Sugar Added, NET WT 56 oz (3 LB 8 OZ) 1.59kg lb), UPC 6 42628 10359 8. Case UPC code: 10642628103526 Soft sided 3.5 lb. pouch style package. Each case has 4 pouches.
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-2730-2015·2015-09-09

    Neuro Kinetics I-Portal NOTC System Recalled for Incorrect Investigational Labeling

    Neuro Kinetics is recalling 45 I-Portal NOTC systems because the OVAR research test was sold with an incorrect investigational label.

    Product
    Neuro Kinetics, Inc. (NKI) I-Portal¿ NOTC system with the OVAR research test; a rotary chair system used in vestibular and neuro-otologic diagnostic testing. This device provides no diagnoses nor does it provide diagnostic recommendations.The OVAR test has not yet been cleared by
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2725-2015·2015-09-09

    Transonic Flow Probe Recalled Due to Software Defect

    Transonic Systems Inc is recalling 3 mm Flow Probes due to a software defect that causes flow meters to display incorrect status messages.

    Product
    Transonic Flow Probe, 3 mm, Catalog Number HQC3MP -- Product Usage: to measure flow intra-operatively.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2478-2015·2015-09-09

    Abbott FIRMap 60mm Catheter Recalled for Incorrect Expiration Date Labeling

    Abbott Electrophysiology is recalling 86 units of FIRMap 60mm Catheters because the expiration date was incorrectly printed on the labels.

    Product
    FIRMap 60mm Catheter; Size: 60 mm; Length 50.4 inches French Size Diameter: 8.5F (2.84mm) Model number : USAR064060 Sterile, Rx only Cardiovascular: For use in cardiac electrophysiology procedures to assist in the diagnosis of complex arrhythmias that may be difficult to
    Category
    Medical Device
    Distribution
    19 states
  • LowFDA (Drugs)·D-1416-2015·2015-09-09

    Silarx Lamivudine Oral Solution Recalled for Mismatched Expiration Dates

    Silarx Pharmaceuticals is recalling 576 bottles of Lamivudine Oral Solution because the expiration date on the carton does not match the bottle label.

    Product
    Lamivudine Oral Solution, USP, 10 mg per 1 mL, 240 mL bottle (8 ounces), Rx only, Manufactured by: Silarx Pharmaceuticals, Inc. Carmel, NY 10512, NDC 54838-0566-70
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·120-2015·2015-09-08

    Olli Salumeria Americana Recalls Pork Salami Due to Misbranding

    Olli Salumeria Americana is recalling pork salami products because the packaging lacks an ingredient list, failing to disclose the presence of sulfites from wine.

    Product
    OLLI SALUMERIA AMERICANA — Olli Salumeria Americana, LLC Recalls Pork Products Due To Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1366-2015·2015-09-02

    Mucinex Fast-Max Liquid Recalled for Missing Drug Facts Labeling

    Reckitt Benckiser is recalling Mucinex Fast-Max liquid bottles because the back label is missing active ingredients and safety warnings.

    Product
    Mucinex Fast Max Day Time Severe Cold and Fast-Max Night Time Cold & Flu Two - 6 fl oz (180 mL) bottles Total -12 fl oz (360 mL), For Age 12+, Dist. By: Reckitt Benckiser Parsippany, NJ 07054-0224 Made in India, NDC 63824-526-22
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1367-2015·2015-09-02

    Mucinex Fast Max Liquid Recalled for Missing Drug Facts Labeling

    Reckitt Benckiser is recalling Mucinex Fast Max liquid bottles where the back label is missing active ingredients and safety warnings.

    Product
    Mucinex Fast Max Severe Congestion & Cough, Maximum Strength, Dextromethorphan HBr Cough Suppressant, Guaifenesin Expectorant, Phenylephrine HCl Nasal Decongestant, 6 fl oz (180 mL) Bottle, For Age 12+, Dist. By: Reckitt Benckiser Parsippany, NJ 07054-0224, Made in India, NDC 638
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1363-2015·2015-09-02

    Mucinex Fast-Max Recalled for Missing Drug Facts Labeling

    Reckitt Benckiser is recalling Mucinex Fast-Max liquid bottles because the back label is missing active ingredients and safety warnings.

    Product
    MUCINEX FAST-MAX — MUCINEX FAST-MAX (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1365-2015·2015-09-02

    Mucinex Fast-Max Cold & Sinus Recalled for Missing Drug Facts Labeling

    Reckitt Benckiser is recalling Mucinex Fast-Max Cold & Sinus liquid because the back of the bottle is missing active ingredients and safety warnings.

    Product
    Mucinex Fast-Max Cold & Sinus, Maximum Strength, Acetaminophen Pain Reliever/Fever Reducer, Guaifenesin Expectorant, Phenylephrine HCl Nasal Decongestant, 6 fl oz (180 mL) Bottle, For Ages 12+, Dist. by: Reckitt Benckiser Parsippany, NJ 07054-0224 Made in India, NDC 63824-016-66,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3053-2015·2015-09-02

    Fresh Unlimited Recalls Kale Caesar Pasta Salad Due to Undeclared Eggs

    Fresh Unlimited Inc. is recalling Kale Caesar Pasta Recovery Salad because the product labels failed to declare the allergen eggs.

    Product
    Kale Caesar Pasta Recovery Salad, 3.375# (1530g) INGREDIENTS: COOKED TRI-ROTINI PASTA***CAESAR DRESSING (Soybean Oil, Water, Distilled Vinegar, Romano Cheese*** ALLERGENS: FISH, MILK, WHEAT
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-2451-2015·2015-09-02

    Synthes Trauma Ex-Fix System Recalled for MR Labeling Corrections

    Synthes (USA) Products LLC is recalling the Trauma Ex-Fix System to correct MRI safety labeling. The recall identifies additional part numbers as MR Conditional and notes one serious injury.

    Product
    Synthes Trauma Ex-Fix System (Small, Medium, Distraction Osteogenesis (DO) and Large) ; (S) intended to stabilize and provide treatment for fractures of the small bones, such as the hand, wrist, forearm, foot, and ankle; (M) for the construction of an external fixation frame for
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1364-2015·2015-09-02

    Mucinex Fast Max Liquid Recalled for Missing Drug Facts Labeling

    Reckitt Benckiser is recalling Mucinex Fast Max Night Time Cold & Flu liquid bottles because the back label is missing active ingredients and safety warnings.

    Product
    Mucinex Fast Max Night Time Cold & Flu, Maximum Strength, Acetaminophen Pain Reliever/Fever Reducer, Diphenhydramine HCl Antihistamine/Cough Suppressant, Phenylephrine HCl Nasal Decongestant, 6 fl oz. (180 mL) Bottle, For Ages 12+, Dist. By: Reckitt Benckiser Parsippany, NJ 07054
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1368-2015·2015-09-02

    Mucinex Fast Max Liquid Recalled for Missing Drug Facts Labeling

    Reckitt Benckiser is recalling Mucinex Fast Max liquid bottles because the back label is missing active ingredients and safety warnings.

    Product
    Mucinex Fast Max Day Time Severe Congestion & Cough Night Time Cold & Flu, Maximum Strength, Two - 6 fl oz (180 mL) bottles Total - 12 fl oz (360 mL), For Ages 12+, Dist. by Reckitt Benckiser Parsippany, NJ 07054-0224, Made in India, NDC 63824-528-22-01, NDC 63824-528-22-00, UPC
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2458-2015·2015-09-02

    Medline Recalls Central Line Kits Due to Incorrect Age Labeling

    Medline Industries is recalling Central Line kits due to a printing error that mislabels the intended patient age. The error could lead to use on the wrong patient population.

    Product
    Central Line >34 Weeks Kit. Cardiology department. The Central Line >34 Weeks Kit (DYNDC1987A) is intended for use on patients greater than 34 weeks of age. The central venous catheter, also called a central line, is a long, thin, flexible tube used to give medicines, fluids, n
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-3051-2015·2015-09-02

    Fresh Unlimited Caesar Salad Recalled for Undeclared Egg Allergen

    Fresh Unlimited Inc is recalling Caesar Salad kits because the labels failed to declare the presence of eggs, a major food allergen.

    Product
    Caesar Salad, #5.56 (2,522g) "INGREDIENTS: Romaine Lettuce, Caesar Dressing (Soybean oil, water, distilled vinegar, Romano cheese (pasteurized part skim milk, cheese culture, salt, enzymes),*****" *ALLERGENS** Fish, Milk, Wheat
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-2446-2015·2015-09-02

    Roche cobas b 123 Fluid Pack Recall for Low PO2 Results

    Roche is recalling 82 cobas b 123 Fluid Packs due to a calibration issue that may cause erroneously low PO2 results in patient samples.

    Product
    cobas b 123 Fluid Pack COOX REF 05169992001 200 Product Usage: The cobas b 123 POC system is a fully automated POC system for whole blood in vitro measurement of pH, blood gases (B3G), electrolytes NAT, K+, iCaWt (ISE), hematocrit (THct), metabolites (GLu, Lac) total hemoglob
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3049-2015·2015-09-02

    Veggie Evolution Kale Crisps Recalled for Undeclared Milk Allergen

    It Takes A Village Foods is recalling Veggie Evolution Kale Crisps Lemon Parmesan because the label lists Parmesan cheese but fails to declare milk as an allergen.

    Product
    Kale Crisps Lemon Parmesan sold under brand Veggie Evolution, each plastic package has a net weight 1.5 oz. There are six packages per case. UPC is 7 94504 69431 4. The product's label is read in part: "***VEGGIE EVOLUTION***KALE CRISPS***LEMON PARMESAN***INGREDIENTS: KALE,
    Category
    Food
    Distribution
    22 states
  • HighFDA (Food)·F-3050-2015·2015-09-02

    Veggie Evolution Vegetable Crisps Recalled for Undeclared Milk Allergen

    It Takes A Village Foods, LLC is recalling Vegetable Crisps Lemon Parmesan because the label declares Parmesan cheese but fails to declare milk as an allergen.

    Product
    Vegetable Crisps Lemon Parmesan sold under brand Veggie Evolution, each poly pouch has a net weight 2 oz. There are 6 packages per case. UPC is 7 36211 15015 8. The product's label is read in part: "***VEGGIE EVOLUTION***VEGETABLE CRISPS***LEMON PARMESAN***INGREDIENTS: CARROTS
    Category
    Food
    Distribution
    22 states
  • HighFDA (Food)·F-3048-2015·2015-09-02

    Veggie Evolution Kale Crisps Recalled for Undeclared Soy

    It Takes A Village Foods is recalling Veggie Evolution Kale Crisps Zen Nori because the product contains soy, which is not declared on the label.

    Product
    Kale Crisps Zen Nori product is seaweed flavored dehydrated kale chip, sold under brand Veggie Evolution, each poly pouch has a net weight 1.5 oz. There are six packages per case. UPC is 7 13757 57480 8. The product's label is read in part: "***VEGGIE EVOLUTION***KALE CRISPS*
    Category
    Food
    Distribution
    22 states