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.

7551–7575 of 9611

  • ModerateFDA (Devices)·Z-0923-2014·2014-02-12

    Highland Metals Recalls SuperElastic NiTi Orthodontic Archwires Due to Labeling Errors

    Highland Metals, Inc. is recalling SuperElastic NiTi orthodontic archwires because some packages are mislabeled, potentially containing the wrong arch type.

    Product
    SuperElastic Regular force NiTi lower or upper Natural arches. 0.14 size 10 or 100 count packages. Highland Metals Inc. San Jose, CA The devices are intended to provide force to the teeth to effect movement in order to alter their position.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0934-2014·2014-02-12

    OrthoPediatrics Recalls 3.5mm Locking Cortical Bone Screws Due to Packaging Error

    OrthoPediatrics is recalling 12 units of 3.5mm Locking Cortical Bone Screws because the packages incorrectly contain non-locking screws.

    Product
    3.5mm Locking Cortical Bone Screw, T15 Hexalobe, Self Tapping, 20mm Part No. 00-0903-2620 OrthoPediatrics Pediloc" Tibia Plates are indicated for fractures, osteotomies, and non-unions of the pediatric and small stature adult tibia. The subject recalled device is a Bone Screw
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-0904-2014·2014-02-12

    Horiba Medical Recalls ABX PENTRA N Control for Revised Potassium Values

    Horiba Medical is recalling ABX PENTRA N Control units because the product was updated to include a revised Target Value assignment for Potassium.

    Product
    ABX PENTRA N Control, Model No. A11A01653 The ABX PENTRA N Control is for use in quality control by monitoring accuracy and precision for the quantitative methods as specified in the enclosed annex.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0922-2014·2014-02-12

    Highland Metals Recalls SuperElastic NiTi Archwires Due to Labeling Errors

    Highland Metals, Inc. is recalling SuperElastic NiTi archwires because some packages labeled 'Upper' contain 'Lower' archwires and vice versa.

    Product
    SuperElastic Regular force NiTi lower or upper Natural arches. 0.16 size 10 or 100 count packages. Highland Metals Inc. San Jose, CA The devices are intended to provide force to the teeth to effect movement in order to alter their position.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0935-2014·2014-02-12

    Zest Anchors Recalls Locator Implant Attachment Systems Due to Labeling Error

    Zest Anchors is voluntarily recalling specific lots of Locator Implant Attachment Systems because the product labels incorrectly state the final torque for the abutment.

    Product
    LOCATOR¿ Implant Attachment System. The LOCATOR¿ Implant Attachment System is a universal hinge, resilient attachment for endosseous implants. The LOCATOR¿ Implant Attachment System is designed for use with overdentures or partial dentures, retained in whole or in part, by end
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0910-2014·2014-02-12

    Nipro Diagnostics Recalls TRUEtrack Blood Glucose Monitors Due to Unit Error

    Nipro Diagnostics is recalling 105 TRUEtrack blood glucose monitors because they were manufactured with an incorrect factory set unit of measure.

    Product
    MooreMedical Supporting Health & Care...MooreBrand Blood Glucose Monitor for Self-Testing & Multi-Patient Use TRUEtrack. Manufactured by: NIPRO DIAGNOSTICS, Fort Lauderdale, FL 33309 U.S.A. Is intended for the quantitative determination of glucose in human whole blood taken fr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0924-2014·2014-02-12

    Horiba Medical Recalls ABX PENTRA Urine Control L/H for Creatinine Range Update

    Horiba Medical is recalling ABX PENTRA Urine Control L/H because the target range for the Creatinine assay was updated. The recall affects 531 units distributed in the US and Canada.

    Product
    ABX PENTRA Urine Control L/H. The ABX PENTRA Urine Control L/H is a two-level (Low and High) quality control consisting of liquid solutions prepared from human urine with chemical additives and materials of biological origin added as required to obtain given component levels
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·014-2014·2014-02-11

    Utah Firm Recalls Beef Jerky for Undeclared Soy Allergen

    Prime Snax Inc. is recalling approximately 90,000 pounds of beef jerky products because they contain soy lecithin, a known allergen not declared on the label.

    Product
    Prime Snax Inc. — Utah Firm Recalls Various Beef Jerky Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1463-2014·2014-02-05

    NatureBox Picante Ranch Mix Recalled for Missing Wheat Allergen Labeling

    NatureBox is recalling Picante Ranch Mix because the ingredient list failed to disclose unbleached wheat flour and bulgur wheat.

    Product
    NatureBox Picante Ranch Mix Spicy Snack Mix with Corn Nuts and Masa Chips; Net. WT: 4 oz. (113 g), Stand up Pouch, Vegan Ingredients: Corn Nuts (corn, canola oil, soybean oil, salt), Sugar, Flax Chips (Yellow corn masa, flax seeds, soybean oil, salt) Snack Seasoning(sour cr
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1434-2014·2014-02-05

    Lambs Farm Raspberry Swirl Bread Recalled for Undeclared Soy Allergen

    The Lambs Farm, Inc. is recalling Raspberry Swirl Bread loaves sold in Bread Trio gift boxes because the labels do not declare soy allergens.

    Product
    Raspberry Swirl Bread loaf sold under the Lambs Farm brand and packaged in a plastic bag with a net weight of 8 oz. This product was only sold as a part of the Bread Trio gift box.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1429-2014·2014-02-05

    Lambs Farm Double Chocolate Butter Cookies Recalled for Allergen Mislabeling

    The Lambs Farm, Inc. is recalling Double Chocolate Butter Cookies because the labels do not declare milk and wheat allergens.

    Product
    Double Chocolate Butter Cookies sold under the Lambs Farm brand and packaged in a plastic bag with a net weight of 10 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1432-2014·2014-02-05

    Lambs Farm Snowball Cookies Recalled for Undeclared Allergens

    The Lambs Farm, Inc. is recalling Snowball Cookies because the labels fail to declare milk, soy, and wheat allergens.

    Product
    Snowball Cookies sold under the Lambs Farm brand and packaged in a white metal tin with a net weight of 1 lb.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F1462-2014·2014-02-05

    NatureBox Salsa Spiced Nut Mix Recalled for Missing Wheat Allergen Labeling

    NatureBox is recalling 8,672 bags of Salsa Spiced Nut Mix because the ingredient list failed to disclose unbleached wheat flour and bulgur wheat.

    Product
    NatureBox Salsa Spiced Nut Mix; Net. WT: 4 oz. (113 g), Stand up Pouch, Vegan Ingredients: Almonds, Corn chips with flax (yellow corn masa, flax seed, soybean oil, salt), Cashews, seasoning ( tomato powder, salt, sugar, onion powder, garlic powder, spices, cilantro, lime juice
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1436-2014·2014-02-05

    Lambs Farm Blueberry Bread Recalled for Undeclared Soy Allergen

    The Lambs Farm, Inc. is recalling Blueberry Bread loaves sold in Bread Trio gift boxes because the labels do not declare soy allergens.

    Product
    Blueberry Bread loaf sold under the Lambs Farm brand and packaged in a plastic bag with a net weight of 8 oz. This product was only sold as a part of the Bread Trio gift box.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1435-2014·2014-02-05

    Lambs Farm Banana Nut Bread Recalled for Undeclared Soy Allergen

    The Lambs Farm, Inc. is recalling Banana Nut Bread loaves sold in Bread Trio gift boxes because the labels do not declare soy allergens.

    Product
    Banana Nut Bread loaf sold under the Lambs Farm brand and packaged in a plastic bag with a net weight of 8 oz. This product was only sold as a part of the Bread Trio gift box.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1433-2014·2014-02-05

    Lambs Farm Cookie Combo Recalled for Undeclared Milk and Wheat Allergens

    The Lambs Farm, Inc. is recalling Cheerful Cookie Combo tins because the labels fail to declare milk and wheat allergens.

    Product
    Cheerful Cookie Combo containing an assortment of Lemon Butter Cookies and Famous Butter Cookies sold under the Lambs Farm brand and packaged in a white metal tin with a net weight of 1 lb.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0901-2014·2014-02-05

    Merit Medical Systems Recalls RAD BOARD Devices Due to Missing Labels

    Merit Medical Systems is voluntarily recalling one lot of RAD BOARD devices because missing labels may allow incorrect orientation, potentially obscuring patient anatomy during fluoroscopy.

    Product
    Radial Assist RAD BOARD, used to support the weight of a patient's arm and supplies for a medical procedure. The Merit RAD BOARD is a rigid and stiff body board intended for use for various medical purposes. RAD BOARD was specifically designed to support the weight of a patie
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-0829-2014·2014-02-05

    Anspach Recalls Single-Use Sterile Bone Cutting Burs Due to Length Discrepancy

    The Anspach Effort, Inc. is recalling 599 single-use sterile bone cutting burs because the cutters were longer than stated on the label.

    Product
    AnspacSingle use Sterile bone cutting burs.h REF: S-1504TD Twist Drill for 1.5mm x 4mm screw. Rx only Single use Sterile bone cutting burs.
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-0830-2014·2014-02-05

    Anspach Twist Drill Recall Due to Incorrect Length Labeling

    The Anspach Effort, Inc. is recalling 29 single-use sterile twist drills because the cutters were longer than stated on the label.

    Product
    Anspach REF: TURQ-434-4 Twist Drill for 1.5mm x 4mm screw. Rx only Single use Sterile bone cutting burs.
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-0847-2014·2014-02-05

    Zimmer Dental Recalls Tapered Screw-Vent Implant Lot Due to Labeling Error

    Zimmer Dental is voluntarily recalling a specific lot of Tapered Screw-Vent Implants because some packages may display incorrect size information on the cap label.

    Product
    Tapered Screw-Vent Implant, MTX, 4.7mm x 11.5mm, 4.5mm Platform. Catalog Number TSVWB11, Lot 62470008. Class II, 510(k) K13227.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0868-2014·2014-02-05

    Siemens Free T3 Assay Kits Recalled for Positive Bias in Results

    Siemens Healthcare Diagnostics is recalling Free T3 Assay kits due to a positive bias that may cause normal thyroid patients to appear abnormal.

    Product
    T3F, Free T3 Assay, REF/Catalog Number L2KF32 (200 tests), Siemens Material Number (SMN) 10381675, and REF/Catalog Number L2KF36 (600 Tests), SMN 10381682; an IVD Immunoassay kit for use with the IMMULITE 2000/IMMULITE 200 XPi Analyzers --- Origin: UK Siemens Healthcare Diagnost
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0867-2014·2014-02-05

    Siemens Free T3 Assay Kits Recalled for Positive Bias in Results

    Siemens Healthcare Diagnostics is recalling Free T3 Assay kits due to a positive bias that may cause normal thyroid patients to appear abnormal.

    Product
    T3F, Free T3 Assay, REF/Catalog Number LKF31, Siemens Material Number (SMN) 10381626; an IVD Immunoassay kit for use with the IMMULITE/IMMULITE 1000 Analyzers --- Shipping or unit package: 100, 200, 500 and 600 test kits --- Origin: UK Siemens Healthcare Diagnostics Products Lt
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1442-2014·2014-02-05

    LSG Food World Recalls Fu Zhou Vermicelli for Filth and Misbranding

    LSG Food World Inc. is recalling Fu Zhou Vermicelli due to filth and missing English translations. The product was distributed in New York.

    Product
    Lam Sheng Kee Fu Zhou Vermicell, Net Wt. 4.4 LB (2000 g), product is packaged in plastic bag with twelve (12) bags per carton. UPC 6949682 803360; Manufactured by LAM SHENG KEE (HK) INTERNATIONAL LIMITED RM3. 8/F, YUEXIU BLDG., 160-174 LOCKHART ROAD, WAN CHAI HK; Distributed by
    Category
    Food
    Distribution
    1 state