The Recall Desk

Hazard

Mis Labeling recalls

9,607 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,607
Critical
160
Severe
588
Most recent
2026-09-10

Of the 9,607 mis labeling recalls we have scored against our rubric, 160 (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.

3976–4000 of 9607

  • SevereFDA (Drugs)·D-0282-2018·2018-02-07

    Medline Recalls Subpotent Povidone-Iodine Prep Pads

    Medline Industries is recalling sterile staple remover trays containing subpotent povidone-iodine prep pads. The iodine concentration is below the labeled claim of 0.85%.

    Product
    Medline Staple Remover Tray, Sterile, Single Use Only. Packaged in USA for Medline Industries, Inc., Northfield, IL 60060
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0279-2018·2018-02-07

    Medline Laceration Tray Recalled for Subpotent Povidone-Iodine Concentration

    Medline Industries is recalling 600 cases of Laceration Trays because the Povidone-Iodine prep pads contain less iodine than the label claims.

    Product
    Medline Laceration Tray, Sterile, Single Use Only. Packaged in USA for Medline Industries, Inc., Northfield, IL 60093
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0258-2018·2018-02-07

    Medline Concordia Trunk Kit Recalled for Subpotent Iodine Concentration

    Medline Industries is recalling Concordia Trunk Kits because the povidone-iodine prep pads contain less iodine than the label claims.

    Product
    Medline Concordia Trunk Kit. Packaged for Medline Industries, Inc., Northfield, IL 60093
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0495-2018·2018-02-07

    Siemens Syngo.plaza PACS Software Recalled for Data Security and Integrity Issues

    Siemens Medical Solutions is recalling 47 units of Syngo.plaza PACS software to fix data loss, study mix-ups, and unauthorized access risks.

    Product
    Syngo.plaza Picture Archiving and Communication System (PACS) with software version VB20A; Model numbers: 10863171, 10863172, 10863173 Syngo.plaza is a Picture Archiving and Communication System (PACS) software device intended to display, process, read, report, communicate, di
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0758-2018·2018-02-07

    Clover Valley Iced Oatmeal Cookies Recalled for Undeclared Allergens

    Dollar General is recalling Clover Valley Iced Oatmeal Cookies because they are actually Coconut Macaroon Cookies containing undeclared milk and tree nuts.

    Product
    Clover Valley¿ Iced Oatmeal Cookies NET WT 12 OZ (340 g) CONTAINS: WHEAT, SOY. DISTRIBUTED BY DOLGENCORP, LLC 100 MISSION RIDGE GOODLETTSVILLE, TN 37072 UPC 0 86106 03201 5
    Category
    Food
    Distribution
    44 states
  • HighNHTSA·18V096000·2018-02-07

    Audi Recalls S7 and RS7 Models for Incorrect Tire Weight Label

    Volkswagen Group of America is recalling 2014-2018 Audi S7 and RS7 vehicles because the tire information label lists an incorrect maximum weight, which could lead to vehicle overload.

    Product
    AUDI — AUDI S7, RS 7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0644-2018·2018-02-07

    Coat & Bake Chicken Seasoning Recalled for Undeclared Milk Allergen

    Gilster-Mary Lee Corp. is recalling Coat & Bake Original Chicken seasoning because some packages contained pork seasoning with undeclared milk.

    Product
    Coat & Bake, Original Chicken, Seasoned Coating Mix For Chicken, Net Wt 5.5 OZ (156 g), Distributed by SuperValu Inc., Eden Prairie, MN.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0701-2018·2018-02-07

    Sun Noodle Tonkotsu Ramen Recalled for Undeclared Fish Allergen

    Sun Noodle New Jersey, LLC is recalling Tonkotsu Ramen because the flavor packet contains undeclared fish (sardines). Consumers with fish allergies should not eat the product.

    Product
    Sun Noodle brand Tonkotsu Ramen, Packaged in plastic clear clamshell, Banded with Tonkotsu label, distinguishable with a yellow color. (12/case); UPC 0 85315 40003 5
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-0414-2018·2018-02-07

    Exactech Recalls 30 Mislabeled Equinoxe Shoulder Implant Components

    Exactech is recalling 30 Equinoxe Cage, Glenoid, Alpha, Small components due to potential mislabeling. The devices were distributed to facilities in 15 US states, Puerto Rico, and Switzerland.

    Product
    Equinoxe Cage, Glenoid, Alpha, Small Product Usage: The Equinoxe Shoulder System is indicated for use in skeletally mature individuals with degenerative diseases or fractures of the glenohumeral joint where total or hemi- arthroplasty is determined by the surgeon to be the pr
    Category
    Medical Device
    Distribution
    15 states
  • ModerateFDA (Drugs)·D-0269-2018·2018-02-07

    Medline Sheath Removal Kit Recalled for Subpotent Iodine Concentration

    Medline Industries is recalling 40 cases of Sheath Removal Kits because the iodine concentration is below the labeled claim.

    Product
    Medline Sheath Removal Kit, Sterile, Single use only. Packaged in Mexico for Medline Industries, Inc., Northfield, IL 60063
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0415-2018·2018-02-07

    Exactech Recalls 30 Equinoxe Shoulder Implants Due to Mislabeling

    Exactech is recalling 30 Equinoxe shoulder implants because they may be mislabeled. The devices were distributed to facilities in 15 US states, Puerto Rico, and Switzerland.

    Product
    Equinoxe Cage, Glenoid, Alpha, Medium Product Usage: The Equinoxe Shoulder System is indicated for use in skeletally mature individuals with degenerative diseases or fractures of the glenohumeral joint where total or hemi- arthroplasty is determined by the surgeon to be the p
    Category
    Medical Device
    Distribution
    15 states
  • ModerateFDA (Drugs)·D-0305-2018·2018-02-07

    Medline Incision Drainage Kit Recalled for Subpotent Iodine Content

    Medline is recalling Incision Drainage Kits because the iodine content is below the labeled claim. The product was distributed nationwide and internationally.

    Product
    Medline Incision Drainage Kit, Sterile, Single Use Only. Packaged in Mexico by Medline Industries, Inc., Mundelein, IL 60060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0310-2018·2018-02-07

    Medline Suture Removal Tray Recalled for Subpotent Iodine Content

    Medline Industries is recalling Suture Removal Trays because the Povidone-Iodine prep pads contain less iodine than labeled.

    Product
    Medline Suture Removal Tray, Sterile, Single Use Only. Packaged in Mexico by Medline Industries, Inc., Mundelein, IL 60060
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0251-2018·2018-02-07

    Premier Pharmacy Labs Recalls Mitomycin Vials Due to Labeling Error

    Premier Pharmacy Labs is recalling 193 vials of Mitomycin 40 mg/mL due to a label error on the declared strength.

    Product
    Mitomycin 40 mg/mL Preservative Free Irrigation Volume: 10 mL SDV , Compounded by: Premier Pharmacy Labs 8265 Commercial Way, Weeki Wachee, FL 34613, NDC: 69623-160-35.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0252-2018·2018-02-07

    Medline Recalls Povidone-Iodine Prep Pads Due to Low Iodine Content

    Medline Industries is recalling Aplicare Povidone-Iodine Prep Pads because the iodine content is below the labeled claim.

    Product
    Aplicare Povidone-Iodine Prep Pad, Antiseptic, Sterile Solution, Active Ingredient: Povidone-iodine USP 10%. Aplicare, INC., Meriden, CT 06450 USA. NDC: 52380-0111-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0643-2018·2018-01-31

    Grand Central Bakery Recalls Potato Buns for Milk Allergen Mislabeling

    Grand Central Bakery Inc. is recalling 92 bags of Potato Buns because the label fails to declare milk in the 'Contains' statement, despite listing it in ingredients.

    Product
    Potato Buns, 4 pieces packaged in poly bag, net wt.11.8 oz. The label is read in parts: "***POTATO BUNS***NET WT. 11.8 OZ***Ingredients:***Enriched unbleached wheat flour***buttermilk powder, butter ***Contains: wheat, dairy***".
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0406-2018·2018-01-31

    Smith & Nephew Recalls Radial Osteotome Blades Due to Incorrect Expiration Dates

    Smith & Nephew is recalling nine Radial Osteotome Blades because the expiration dates on the labels are incorrect. The devices were distributed in the US and Australia.

    Product
    Radial Osteotome Blade, REF 71369314. Used for cutting or preparing bone.
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0397-2018·2018-01-31

    Smith & Nephew Recalls Mislabeled Mini-Fragment Bone Plating System Devices

    Smith & Nephew is recalling two units of bone plates and screws that were incorrectly labeled as one model but contained a different model.

    Product
    smith&nephew Mini-Fragment Plating System, VLP(R) Mini-Mod Small Bone Plating System, EVOS(R) Mini Plating system, 2.0MM STOUT STRAIGHT PLATE, 8 HOLE VLP(R) MIN-MOD, REF 74442030, QTY: (1), STERILE R Bone plates and bone screws from the Smith & Nephew Variable-Angle Locking Mi
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Food)·F-0642-2018·2018-01-31

    Grand Central Bakery Recalls Hot Dog Buns for Labeling Error

    Grand Central Bakery Inc. is recalling 90 bags of hot dog buns in Washington because the label failed to list milk in the 'Contains' statement.

    Product
    Hot Dog Buns, 6 pieces packaged in a poly bag, net wt 17.3 oz. The label is read in parts: "***HOTDOG BUNS***NET WT. 17.3 OZ***Ingredients:***Enriched unbleached wheat flour***egg, whole milk (milk, vitamin A, vitamin D3), butter***Contains: wheat, egg, dairy***".
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0396-2018·2018-01-31

    Smith & Nephew Mini-Fragment Plating System Recalled for Labeling Error

    Smith & Nephew is recalling two units of bone plates due to incorrect labeling of the plate type.

    Product
    smith&nephew Mini-Fragment Plating System, VLP(R) Mini-Mod Small Bone Plating System, EVOS(R) Mini Plating system, 2.0MM STRAIGHT PLATE, 8 HOLE VLP(R) MIN-MOD, REF 74442024, QTY: (1), STERILE R Bone plates and bone screws from the Smith & Nephew Variable-Angle Locking Mini-Fr
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0392-2018·2018-01-31

    BD MAX Vaginal Panel Recalled for Unresolved and Indeterminate Test Results

    Becton Dickinson is recalling the BD MAX Vaginal Panel due to an increased rate of unresolved and indeterminate results, which may require repeat testing.

    Product
    BD MAXTM Vaginal Panel. Catalog Number(s): 443712 443710 443711 (RUO)for collection and transport of vaginal and endocervical swab specimens, in addition to the preservation of urine from males and females.
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-0398-2018·2018-01-31

    Anspach Effort Recalls Oscillating Saw Attachment Due to Shipping Error

    The Anspach Effort, Inc. is voluntarily recalling one oscillating saw attachment because it was mistakenly shipped to a non-veterinary customer.

    Product
    OSCILLATING SAW ATTACHMENT Surgical instrument motors and accessories/attachments are intended for use during surgical procedures to cut hard tissue or bone and soft tissue.
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·18V073000·2018-01-29

    Jayco Recalls 2018 Eagle Travel Trailers for Incorrect Weight Labeling

    Jayco is recalling 2018 Eagle travel trailers because the Gross Vehicle Weight Rating label may be incorrect, potentially allowing the vehicle to be overloaded.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·18T001000·2018-01-29

    Vogue Tyre & Rubber Recalls Signature V Tires for Missing Date Codes

    Vogue Tyre & Rubber is recalling specific Signature V tires because they lack date codes on the sidewall, which may prevent owners from identifying recalled tires.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide