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.

5201–5225 of 9610

  • ModerateFDA (Devices)·Z-0331-2017·2016-11-09

    Arrow Hands-Off Infusion Port Thermodilution Catheter Recalled for Labeling Inconsistency

    Arrow International Inc is recalling specific lots of Hands-Off Infusion Port Thermodilution Catheters due to a labeling inconsistency. The recall covers 330 units in the US and 1,031 units outside the US.

    Product
    HANDS-OFF Infusion Port Thermodilution Catheter consists of the Arrow IPTD thermodilution catheter enclosed in a contamination shield (Arrow Cath-Gard) with integral flushing/balloon test chamber, enabling the practitioner to prepare, test, and insert the catheter without exposin
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0118-2017·2016-11-09

    Actavis Recalls Ramipril Capsules Due to Incorrect Expiration Date Labeling

    Actavis is recalling 15,984 bottles of Ramipril Capsules because they were labeled with an incorrect expiration date of 03/18 instead of 09/17.

    Product
    Ramipril Capsules, USP, 1.25 mg, 30-count bottle, Rx only, Manufactured by: Arrow Pharm (Malta) Ltd., Birzebbugia, BBG3000, Malta; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054, NDC 16252-570-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·102-2016·2016-11-03

    Flavor Trade Recalls Beef Jerky Produced Without Federal Inspection

    Flavor Trade, LLC. is recalling approximately 113 pounds of beef jerky produced without federal inspection and bearing unauthorized USDA marks.

    Product
    Flavor Trade, LLC. Recalls Beef Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0300-2017·2016-11-02

    Ortho-Clinical Diagnostics Recalls enGen Laboratory Automation System Due to Sample Error

    Ortho-Clinical Diagnostics is recalling the enGen Laboratory Automation System because a software error may cause sample identification to be mismatched with assay results.

    Product
    enGen Laboratory Automation System (Product Code ENGEN) configured with Thermo Scientific Centrifuge Module and TCAutomation Software Version 3.6.1 and Below; IVD. --- Thermo Scientific Centrifuge Module has Product Code 952040-EG 6844097. The VITROS 5,1 FS Chemistry System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0281-2017·2016-11-02

    Bob's Red Mill Guar Gum Recalled for Misidentified Ingredient

    Bob's Red Mill is voluntarily recalling one lot of Guar Gum due to the inclusion of a misidentified ingredient, hydroxyethylcellulose.

    Product
    Label reads in part "*** Bob's Red Mill *** PREMIUM GUAR GUM SUPERB GLUTEN FREE THICKENER & BINDER *** NET WT 8 OZ ***" Product is packaged in multilayered flexible film with multiple colors. Firm brand name is printed in red. Case contains 8/8 oz. packages. UPC 0 39978
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0298-2017·2016-11-02

    TZ Medical Recalls Mis-Labeled Neptune Plus Hemostatic Pads

    TZ Medical is recalling Neptune Plus hemostatic pads because the labels incorrectly state they include an antimicrobial barrier.

    Product
    Neptune Plus (Hemostatic Pad), Part Numbers: 8870-03 Neptune Pad is used to promote the rapid control of bleeding and provide hemostasis for lacerations, abrasions, vascular access sites and following surgical incision. It can be used to achieve hemostasis at the skin surface fo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0319-2017·2016-11-02

    Siemens CMV IgM Assay Recalled for Increased Imprecision

    Siemens Healthcare Diagnostics is recalling IMMULITE CMV IgM Assay kits due to reported increases in imprecision and high coefficient of variation (CV) values.

    Product
    IMMULITE/ IMMULITE 1000 Systems CMM CMV IgM Assay, REF/Catalog Number LKCM1(D) - 100 tests (US), Siemens Material Number (SMN) 10370301 (US), Unique Device Identification Number (UDI) 00630414985718 (US); and REF/Catalog Number LKCM1 - 100 tests (OUS); SMN 10381296 (OUS), UDI 00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0312-2017·2016-11-02

    Becton Dickinson Recalls PhoenixSpec AP Calibrator Due to Labeling Error

    Becton Dickinson is recalling 94 units of PhoenixSpec AP Calibrator because the expiration date year is incorrectly labeled on the kit.

    Product
    PhoenixSpec AP Calibrator is used to calibrate the PhoenixSpec & Phoenix AP Instruments. The instruments are then used to measure the turbidity of microbial suspensions equivalent to McFarland standards 0.10 to 4.50.
    Category
    Medical Device
    Distribution
    17 states
  • LowFDA (Devices)·Z-0311-2017·2016-11-02

    Becton Dickinson Recalls PhoenixSpec Calibrator Kits Due to Labeling Error

    Becton Dickinson is recalling specific lots of BBL PhoenixSpec Calibrator kits because the kits are labeled with an incorrect expiration year, although the individual tubes have correct dates.

    Product
    PhoenixSpec Calibrator & Kit is used to calibrate the PhoenixSpec &#38 Phoenix AP Instruments. The instruments are then used to measure the turbidity of microbial suspensions equivalent to McFarland standards 0.10 to 4.50.
    Category
    Medical Device
    Distribution
    17 states
  • LowFDA (Drugs)·D-0115-2017·2016-11-02

    Invokamet Recalled for Incorrect or Missing Package Insert Labeling

    Janssen Ortho L.L.C. is recalling Invokamet tablets because Xarelto prescribing information outserts may be affixed to the bottles instead of the correct Invokamet inserts.

    Product
    INVOKAMET — INVOKAMET (CANAGLIFLOZIN AND METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·16V786000·2016-10-28

    Starcraft RV Recalls 2017 AR-ONE Trailers for Incorrect Load Labels

    Starcraft RV is recalling 94 model year 2017 AR-ONE trailers because incorrect Federal Placard and Cargo Carrying Capacity labels may lead to overloading and increased crash risk.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT AR-ONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V787000·2016-10-28

    Forest River Recalls 2017 Salem and Wildwood Trailers for Labeling Errors

    Forest River is recalling 92 model year 2017 Salem and Wildwood recreational trailers because the Federal Placard Label and VIN incorrectly state the vehicles have two axles instead of one.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0209-2017·2016-10-26

    New Seasons Market Recalls Almond Butter Labeled Incorrectly as Peanut Butter

    New Seasons Market is recalling Creamy Almond Butter because some jars labeled as almond butter actually contain peanut butter. This labeling error poses a risk to consumers with peanut allergies.

    Product
    New Seasons Market Creamy Almond Butter 16oz; Label reads in part "***NEW SEASONS WILD FRIENDS FOODS PORTLAND, OR *** IT'S A JAR OF ALMOND BUTTER CREAMY A hint of Jacobsen Sea Salt***" UPC 4060010401;
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0113-2017·2016-10-26

    Mei Shun Rice Noodles Recalled for Undeclared Allergens

    Louis Hong Inc Dba Mei Shun Noodle Inc is recalling 6 Five Rice Noodles due to undeclared shrimp, soybean oil, and green onions.

    Product
    6 Five, Rice Noodles, Keep Refrigerated, Ingredients: Rice flour, water, salt and corn oil. Weight: 12 oz, Manufactured by: Mei Shun Noodle Inc, 610 W. 26th Street Chicago IL 60613, (312) 842-6500. Noodles on styrofoam tray visible through clear plastic wrap.
    Category
    Food
    Distribution
    1 state
  • CriticalUSDA FSIS·101-2016·2016-10-26

    Gaiser's Recalls Chicken and Pork Bologna Due to Undeclared Milk Allergen

    Gaiser's European Style Provision Inc. is recalling approximately 3,895 pounds of chicken and pork bologna products due to misbranding, undeclared milk allergens, and uninspected meat.

    Product
    Gaiser's European Style Provisions Inc. — Gaiser's European Style Provision Inc. Recalls Chicken and Pork Bologna Products Due to Misbranding, Undeclared Allergens, and Being Formulated with Uninspected Meat and Poultry Products
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Drugs)·D-0104-2017·2016-10-26

    Dietary Supplement Recalled for Undeclared Sildenafil and Analogs

    SOS Telecom Inc. is recalling Super Samurai-X dietary supplements because FDA testing found undeclared sildenafil and/or its analogs.

    Product
    Super Samurai-X , 1000 mg, 1 capsule per pack , 24 single packs per box.
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-0189-2017·2016-10-26

    Birdy 3 in 1 Coffee Mix Recalled for Undeclared Milk Allergen

    Food Gusto, Inc. is recalling Birdy 3 in 1 Robusta Coffee Mix because it may contain undeclared milk and has unclear nutritional labeling.

    Product
    Birdy 3 in 1 Robusta Coffea Mix, 445.5 g in a red sealed plastic bag, Product of Thailand, UPC 8850250007425
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0154-2017·2016-10-26

    Union Bagel Shop Recalls Italian Bagels for Undeclared Wheat

    Union Bagel Shop is recalling Italian bagels sold in Grande, Oregon, due to undeclared wheat. The voluntary recall was initiated by the firm.

    Product
    Package contains a business card for "***BAGEL SHOP***" "***Italian: Flour, Filtered Water, Organic Shortening, Olive Oil, Malt, Sugar, Sea Salt, Yeast, Organic Marinara Sauce, Oregano.***" 2 bagels per package - plastic bag with twist tie.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0151-2017·2016-10-26

    Union Bagel Shop Recalls Plain Bagels Due to Undeclared Wheat

    Union Bagel Shop is recalling plain bagels because the packaging fails to declare wheat, a major food allergen.

    Product
    Package contains a business card for "***BAGEL SHOP***" "***Plain: Flour, Filtered Water, Organic Shortening, Olive Oil, Malt, Sugar, Sea Salt, Yeast.***" 2 bagels per package - plastic bag with twist tie.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0149-2017·2016-10-26

    Union Bagel Shop Recalls Bagels for Undeclared Wheat

    Union Bagel Shop is recalling bagels sold in Grande, Oregon, due to undeclared wheat, a major food allergen.

    Product
    Package contains a business card for "***BAGEL SHOP***" "***Pretzel Salt: Flour, Filtered Water, Organic Shortening, Olive Oil, Malt, Sugar, Sea Salt, Yeast, Pretzel Salt.***" 2 bagels per package - plastic bag with twist tie.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0150-2017·2016-10-26

    Union Bagel Shop Recalls Onion and Garlic Bagels for Undeclared Wheat

    Union Bagel Shop is recalling Onion/Garlic bagels due to undeclared wheat. The product was sold at one retail store in Grande, Oregon.

    Product
    Package contains a business card for "***BAGEL SHOP***" "***Onion/Garlic: Flour, Filtered Water, Organic Shortening, Olive Oil, Malt, Sea Salt, Sugar, Yeast, Onion & Garlic Flakes.***" 2 bagels per package - plastic bag with twist tie.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0162-2017·2016-10-26

    Union Bagel Shop Cowboy Cookies Recalled for Undeclared Allergens

    Union Bagel Shop is recalling Cowboy Cookies In-a-Jar because the packaging fails to declare wheat, milk, and soy allergens.

    Product
    Package contains a business card for "***BAGEL SHOP***" "***Cowboy Cookies In-a- Jar***INGREDIENTS: FLOUR, ROLLED OATS, BROWN SUGAR, BAKING POWDER, SALT, SUGAR, M & M's***" This information was hand written on a business card, no separate ingredient statement.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0156-2017·2016-10-26

    Union Bagel Shop Recalls Sesame Seed Bagels Due to Undeclared Wheat

    Union Bagel Shop is recalling sesame seed bagels because the packaging fails to declare wheat as an ingredient. The product was sold at one retail store in Grande, Oregon.

    Product
    Package contains a business card for "***BAGEL SHOP***" "***Sesame Seed: Flour, Filtered Water, Organic Shortening, Olive Oil, Malt, Sugar, Sea Salt, Yeast, Organic Sesame Seeds.***" 2 bagels per package - plastic bag with twist tie.
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-0167-2017·2016-10-26

    Nature's One Organic PediaSmart Beverage Recalled for Incorrect Scoop Size

    Nature's One is recalling Organic PediaSmart Dairy Vanilla beverage cans because they contain a scoop that provides only 60% of the intended nutrition.

    Product
    Nature's One, Organic PediaSmart¿ Dairy Vanilla complete nutrition beverage for kids 1 to 13 years NET WT 12.7 oz (360 G) can Contains: milk, soy & coconut UPC 7 16514 88101 0 Manufactured for: Natures One, 8754 Cotter Street, Lewis Center, OH 43035
    Category
    Food
    Distribution
    49 states