The Recall Desk

Hazard

Mis Labeling recalls

9,611 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,611
Critical
161
Severe
589
Most recent
2026-09-24

Of the 9,611 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 589 (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.

6951–6975 of 9611

  • ModerateFDA (Food)·F-0466-2015·2014-11-12

    Mama Tere Arepa de Moto Hominy Patties Recalled for Mislabeling

    Family Food Distributors, Inc. is recalling Mama Tere Arepa de Moto Hominy Patties because the product was found to be mislabeled.

    Product
    Mama Tere Arepa de Moto Hominy Patty 14.1 oz / 400 g 5 units Product of Colombia Importado Por: Family Food Distributors, Inc. 969 Newark Turnpike, Kearny, NJ 07032 UPC 812828011652
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-0164-2015·2014-11-12

    Siemens Calibrator E Recalled for Positive Bias in Cortisol and Progesterone Assays

    Siemens Healthcare Diagnostics is recalling Calibrator E kits due to positive bias in Cortisol and Progesterone assays on ADVIA Centaur Systems.

    Product
    Siemens Calibrator E; SMN 10309079 (2 pack), SMN 10321075 (6 pack), SMN 10335532 (6 pack Ref)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·077-2014·2014-11-09

    Kulana Foods Recalls Frozen Pork Products Due to Undeclared Wheat Allergen

    Kulana Foods is recalling approximately 4,465 pounds of frozen, fully cooked pork products because they contain wheat, a known allergen, that is not declared on the label.

    Product
    Kulana Foods, Ltd. — Hawaii Firm Recalls Frozen Pork Products Due To Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·14V711000·2014-11-07

    Dodge Journey Recall for Inaccurate Tire Placard Weight Information

    Chrysler is recalling 2014-2015 Dodge Journey vehicles because tire placard labels may contain inaccurate weight and seating information, increasing crash risk.

    Product
    DODGE — DODGE JOURNEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0085-2015·2014-11-05

    Pillsbury Biscuits Recalled for Undeclared Milk Ingredient

    General Mills is recalling specific cases of Pillsbury Biscuits Buttermilk 4pk due to incorrect overwrap labeling that fails to declare milk.

    Product
    Cases of refrigerated Pillsbury Biscuits Buttermilk 4pk. (6 - 4pk / case)
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-0130-2015·2014-11-05

    Siemens Recalls ADVIA Centaur Ferritin Calibrator C Due to Realignment Issue

    Siemens Healthcare Diagnostics is recalling ADVIA Centaur Calibrator C kits due to a realignment issue with Ferritin Analytical Sensitivity. The recall affects 234 kits distributed worldwide.

    Product
    ADVIA Centaur Calibrator C-Used with the ADVIA Centaur Ferritin assay on the ADVIA Centaur CP system only. (In-Vitro Diagnostic) Catalog Number: 672182005 (US Reference 6 pack)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0096-2015·2014-11-05

    Real Foods Recalls Mexican Cheddar Dip for Missing Egg Labeling

    Real Foods of Seattle is recalling 96 units of Mexican Cheddar Dip because egg is missing from the ingredient statement.

    Product
    Mexican Cheddar Dip 10oz non-flex plastic, distributed by Taylor Farms Salinas, CA 93902. The label will show UPC 0 3022300960 9 or UPC 0 30223 00952 8
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0086-2015·2014-11-05

    Pillsbury Biscuit Flaky Layers Recalled for Undeclared Milk Ingredient

    General Mills is recalling Pillsbury Biscuit Flaky Layers 4-packs because the outer packaging incorrectly lists the product, creating a risk of undeclared milk for consumers.

    Product
    Pillsbury refrigerated Biscuit Flaky Layers retail 4pk package.
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-0145-2015·2014-11-05

    Parker Eclipse Probe Covers Recalled for Incorrect Expiration Date Labeling

    Parker Laboratories is recalling Eclipse Probe Covers due to incorrect expiration dates on inner boxes and plastic bags.

    Product
    Parker Eclipse Probe Cover, Latex Free, REF 38-01, 10 Eclipse Probe Covers, Size: 2.37/1.75"W x 9.5"L (60/44 mm x 241 mm), Lot #D424, Expiry date 04/2016, Pre-gelled inside with Aquasonic 100 Ultrasound Transmission Gel Product Usage: For use as a protective cover for medical
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0135-2015·2014-11-05

    Abbott HbA1c Calibrators Recalled for Potential Incorrect Value Sheets

    Abbott Laboratories is recalling HbA1c Calibrators that may contain value sheets for a different lot, which could cause falsely elevated test results.

    Product
    HbA1c Calibrators LN 4P52-02 consists of: 4P52-02 Hemoglobin A1c 1 x 1.6 mL and 1 x 1.6 mL. A1c Calibrators (lyophilized) contain hemoglobin and glycated hemoglobin from human whole blood. Prior to lyophilization, the calibrator matrix is an MES-buffered solution. Preservative: O
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0136-2015·2014-11-05

    Animas Vibe Insulin Pump Recalled for Incorrect Hebrew Translation

    Animas Corporation is recalling 1,028 Vibe Insulin Infusion Pumps in Israel due to incorrect Hebrew language translations and omitted text on the display screen.

    Product
    Animas Vibe Insulin Infusion Pump. This product is indicated for continuous subcutaneous infusion of insulin for the treatment of diabetes and has a continuous glucose monitoring feature.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0131-2015·2014-11-05

    Abbott Lipase Reagent Recalled for Incorrect Package Insert Parameters

    Abbott Laboratories is recalling Lipase Reagent 7D80 because package inserts contain incorrect SmartWash parameters for Triglyceride.

    Product
    Lipase Reagent, 7D80. Used to measure lipase in human serum on the Architect system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0147-2015·2014-11-05

    CooperSurgical Recalls Blunt Hurd Cannula Due to Incorrect Package Insert

    CooperSurgical is recalling 90 units of Blunt Hurd Cannula because the wrong package insert was included in the shipping materials.

    Product
    Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Reducer simplifies open laparoscopy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0153-2015·2014-11-05

    Zimmer Dental Recalls Spline Twist Implants Due to Labeling Error

    Zimmer Dental is recalling 1,044 Spline Twist Implants because the incorrect diameter size was printed on the inner vial.

    Product
    Spline Twist Implant, HA 3.25mmD X 15mmL; Part No. 2135. Zimmer Dental Spline implant systems are designed for use in edentulous mandibles or maxillae for attachment of complete denture prostheses for immediate or conventional loading, or as a terminal or intermediary abutment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0139-2015·2014-11-05

    Biosense Webster Recalls ThermoCool SmartTouch Navigation Catheters for Labeling

    Biosense Webster is recalling ThermoCool SmartTouch Navigation Catheters to provide additional labeling for safe and effective use.

    Product
    ThermoCool SmartTouch Navigation Catheters, Catalog No. D132701, D132702, D132703, D132704, D132705, D133601, D133602, D133603.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0154-2015·2014-11-05

    Zimmer Dental Recalls Tapered Screw-Vent Implants Due to Labeling Error

    Zimmer Dental is recalling specific Tapered Screw-Vent Implants because the incorrect diameter size was printed on the inner vial.

    Product
    Tapered Screw-Vent Implant, MTX, 4.1mmD X 10mmL X 3.5mm Platform Part No. TSV4B10 Tapered Screw-Vent Implant, MTX, 4.1mmD X 11.5mmL X 3.5mm Platform Part No. TSV4B11 The Tapered Screw-Vent Implants are designed for use in the maxilla or mandible for immediate loading or f
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0051-2015·2014-11-05

    Valeant Recalls APLENZIN Tablets Due to Missing Package Insert

    Valeant Pharmaceuticals is recalling 20,499 bottles of APLENZIN (bupropion hydrobromide) 174 mg tablets because the package insert is incorrect or missing.

    Product
    APLENZIN¿ (bupropion hydrobromide), extended-release tablets, 174 mg, 7-count HDPE bottle, Rx Only, Manufactured by Valeant Pharmaceuticals International, Inc. Steinbach MB, Canada R5G 1Z7, NDC 0024-5810-07.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0052-2015·2014-11-05

    Valeant Recalls APLENZIN Tablets Due to Missing Package Insert

    Valeant Pharmaceuticals is recalling APLENZIN extended-release tablets because the package insert is incorrect or missing. Consumers should contact their healthcare provider.

    Product
    APLENZIN¿ (bupropion hydrobromide), extended-release tablets, 348 mg, a) 7-count HDPE bottle (NDC 0024-5811-07), b) 30-count HDPE bottle (NDC 0024-5811-30), Rx Only, Manufactured by Valeant Pharmaceuticals International, Inc. Steinbach MB, Canada R5G 1Z7
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0053-2015·2014-11-05

    Valeant Recalls APLENZIN Tablets Due to Missing Package Insert

    Valeant Pharmaceuticals is recalling APLENZIN (bupropion hydrobromide) extended-release tablets because the package insert is incorrect or missing.

    Product
    APLENZIN¿ (bupropion hydrobromide), extended-release tablets, 522 mg, a) 7-count HDPE bottle (NDC 0024-5812-07), b) 30-count HDPE bottle (NDC 0024-5812-30), Rx Only, Manufactured by Valeant Pharmaceuticals International, Inc. Steinbach MB, Canada R5G 1Z7
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0138-2015·2014-11-05

    Coloplast Recalls Mislabeled Biatain Super Non-Adhesive Wound Dressing Lot

    Coloplast is recalling one lot of Biatain Super Non-Adhesive wound dressings due to mislabeling. The affected units were distributed to Missouri and Rhode Island.

    Product
    Biatain Super Non-Adhesive, Catalog number 46300, 10 pcs, REF 0463001400. Country of Origin:HU. Biatain Super Non-Adhesive dressing is primarily indicated for the treatment of high, medium and low exuding leg ulcers surrounded by fragile skin. The dressings may be used through
    Category
    Medical Device
    Distribution
    2 states
  • HighNHTSA·14V697000·2014-11-04

    Jayco Recalls 2015 Jay Flight Trailers Due to Incorrect Load Labels

    Jayco is recalling 2015 Jay Flight trailers because cargo capacity labels may overstate load limits, creating a risk of tire failure and crashes.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FLIGHT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V696000·2014-11-03

    Jayco Recalls 2015 Eagle Fifth Wheel Trailers for Incorrect Weight Labels

    Jayco is recalling 268 model year 2015 Eagle fifth wheel trailers because incorrect weight calculations on the cargo label could lead to overloading and tire failure.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0076-2015·2014-10-29

    Lotte European Waffles Recalled for Undeclared Eggs

    Lotte International America Corp is recalling Lotte European Waffles because they contain undeclared eggs, posing a risk to consumers with egg allergies.

    Product
    Lotte European Waffle, Net Wt. 40g, 160g UPC 8801062518111, 8801062518135
    Category
    Food
    Distribution
    Distributed nationwide