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.

2376–2400 of 9607

  • ModerateFDA (Devices)·Z-0720-2020·2020-01-01

    Abbott Recalls Mislabeled Radiofrequency Cannulas Due to Manufacturing Error

    Abbott Medical is recalling 470 radiofrequency cannulas that were incorrectly labeled with a 5mm active tip length instead of 10mm.

    Product
    CLASSIC Radiofrequency Cannula - Curved, 10 cm, SMK Compatible Electrode, REF C-1005-S - Product Usage: Disposable Radiofrequency Cannulae are provided in either straight, curved, or curved blunt geometries with a stylet inserted in the cannula. Cannulae are insulated except for
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0732-2020·2020-01-01

    AAP Implantate Drill CS 4.0 Recalled for Incorrect Instructions

    AAP Implantate Ag is recalling 7 units of INTEGRA Drill CS 4.0 in Texas due to incorrect instructions for use.

    Product
    INTEGRA, Drill CS 4.0, quick coupling single use, REF 430425
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-0745-2020·2020-01-01

    Tosoh AIA-PACK B12 Pretreatment Set Recalled for Barcode Reading Errors

    Tosoh Smd Inc is recalling AIA-PACK B12 Pretreatment Sets due to barcode scanning issues that may delay diagnostic results.

    Product
    AIA-PACK B12 Pretreatment Set- IVD for diagnostic use for pre-treatment of calibrators/controls. Part Number: 020706
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0731-2020·2020-01-01

    INTEGRA Drill CS 4.5 Recalled for Incorrect Instructions for Use

    AAP Implantate Ag is recalling two units of INTEGRA Drill CS 4.5 in Texas due to incorrect instructions for use.

    Product
    INTEGRA, Drill CS 4.5, quick coupling single use, REF 430453
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-0337-2020·2019-12-25

    Gold Standard Baking Recalls Croissants Due to Missing Allergen Labels

    Gold Standard Baking is recalling Freshness Guaranteed Croissants because the packaging is missing ingredient and nutrition labels, including required allergen information for milk, wheat, and soy.

    Product
    Freshness Guaranteed Croissants in clear plastic 12oz clamshell, 12 clamshells per case, item number 7012
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0682-2020·2019-12-25

    Polymer Technology Systems Recalls A1CNow+ Systems Due to Software Bug

    Polymer Technology Systems is recalling A1CNow+ Systems because a software bug may display incorrect numerical values instead of expected symbols.

    Product
    A1CNow+ Systems (professional use product), Software Version Revision D, REF Numbers US: 3021, 3024; EU: 3037, 3038, 3057, 3058
    Category
    Medical Device
    Distribution
    18 states
  • ModerateFDA (Devices)·Z-0685-2020·2019-12-25

    ReliOn FastA1C Test Recalled for Software Bug Affecting Result Display

    Polymer Technology Systems is recalling ReliOn FastA1C Tests due to a software bug that may display incorrect numerical values instead of expected symbols.

    Product
    ReliOn FastA1C Test, Software Version Revision D, REF Number 3055
    Category
    Medical Device
    Distribution
    18 states
  • ModerateFDA (Devices)·Z-0683-2020·2019-12-25

    Polymer Technology Systems Recalls A1CNow SELF CHECK Software Bug

    Polymer Technology Systems is recalling A1CNow SELF CHECK devices due to a software bug that may display incorrect numerical values instead of expected symbols.

    Product
    A1CNow SELF CHECK (European), Software Version Revision D, REF Numbers 3054, 3062
    Category
    Medical Device
    Distribution
    18 states
  • ModerateFDA (Devices)·Z-0691-2020·2019-12-25

    Integra Recalls Mislabeled Ascension Silicone PIP Joint Implants

    Integra Lifesciences is recalling nine Ascension Silicone PIP implants that were mislabeled as size 1 but contained size 0 implants.

    Product
    Ascension¿ Silicone PIP-Silicone PIP Sz 1, Model Number: SPIP5201WW - Product Usage: The Ascension Silicone PIP implant is intended for cementless replacement of the proximal interphalangeal joint in patients with advanced osteoarthritis, post-traumatic arthritis and rheumatoi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0708-2020·2019-12-25

    Rhondium OVC3 One Visit Crown Recalled for Incorrect Expiration Date

    Rhondium Limited is recalling six OVC3 One Visit Crown devices because they were mislabeled with an incorrect expiration date.

    Product
    Rhondium OVC3 One Visit Crown, Model FDI 24/25L USA 12/13L A2 HT, Nonsterile, Rx. The firm name on the label is Rhondium Ltd., Katikati, New Zealand.
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0684-2020·2019-12-25

    Polymer Technology Systems Recalls Walgreens At-Home A1C Test Kits

    Polymer Technology Systems is recalling 15,118 Walgreens At-Home A1C Test Kits due to a software bug that may display incorrect numerical values for extreme results.

    Product
    Walgreens At-Home A1C Test Kit, Software Version Revision D, REF Number 3056
    Category
    Medical Device
    Distribution
    18 states
  • ModerateFDA (Devices)·Z-0703-2020·2019-12-25

    Teleflex Sheridan Endobronchial Tubes Recalled for Incorrect Labeling

    Teleflex Medical is recalling Sheridan Endobronchial Tubes due to incorrectly labeled tracheal and bronchial swivel connectors.

    Product
    HUDSON RCI SHERIDAN SHERI-BRONCH Endobronchial Tube REF 5-16135 - Product Usage: The Sheridan Endobronchial Tubes are intended for use in Thoracic surgery, brochospirometry, adminitration of endobronchial anesthesia and other uses commonly requiring endobronchial intubation. The
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0694-2020·2019-12-25

    Tekia Recalls Mislabeled Hydrophilic Acrylic Intraocular Lenses

    Tekia, Inc. is recalling 36 intraocular lenses that may be mislabeled with the incorrect diopter power. No U.S. distribution occurred.

    Product
    TEKIA Model 872 Single Piece Hydrophilic Acrylic Intraocular Lenses, Diopter 15.0, Sterile. The firm name on the label is TEKIA, INC., Irvine, CA.
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-0700-2020·2019-12-25

    Allergan Recalls Natrelle Breast Implants Due to Unreadable 2D Barcodes

    Allergan is recalling Natrelle silicone breast implants because 2D barcodes may be unreadable by GS-1 scanners due to non-standard formatting.

    Product
    Natrelle Silicone Filled Breast Implants for the following Styles and Sizes: Style 10, Style 15, Style 20, Style 40, Style 45 Style 10/UDI: NATRELLE Style 10-180 Gel Round Mod 10888628001206, NATRELLE Style 10-210 Gel Round Mod 10888628001213, NATRELLE Style 10-240 Gel Roun
    Category
    Medical Device
    Distribution
    47 states
  • LowFDA (Devices)·Z-0701-2020·2019-12-25

    Allergan Recalls Breast Implants With Non-Standard 2D Barcodes

    Allergan is recalling Natrelle Inspira silicone-filled breast implants because 2D barcodes may be unreadable by GS-1 scanners due to formatting errors.

    Product
    Natrelle Inspira Sillicone-Filled Breast Implants for the following Styles and Sizes: 7607 SSM, 7608 SSF, 7609 SSX, 7513 SRL, 7514 SRLP, 7515 SRM, 7516 SRF, 7517 SRX, 7626 SCL, 7627 SCLP, 7628 SCM, 7629 SCF, 7630 SCX: 7607 SSM/UDI: Natrelle Inspira SSM 140cc BI (US) 108886280
    Category
    Medical Device
    Distribution
    47 states
  • LowFDA (Devices)·Z-0699-2020·2019-12-25

    Allergan Natrelle Breast Implant Recall for Unreadable 2D Barcodes

    Allergan is recalling Natrelle saline-filled breast implants because 2D barcodes may be unreadable by GS-1 scanners due to formatting errors.

    Product
    Natrelle Saline-Filled Breast Implant, for the following Styles and sizes, Style LP, Style 68 HP, Style 68 MP, Style LP/UDI: NATRELLE Style 68LP-125 Saline Round Low 10888628000513, NATRELLE Style 68LP-150 Saline Round Low 10888628000520, NATRELLE Style 68LP-175 Saline Rou
    Category
    Medical Device
    Distribution
    47 states
  • LowFDA (Devices)·Z-0702-2020·2019-12-25

    Allergan Recalls Breast Implant Sizers Due to Unreadable Barcodes

    Allergan is recalling NATRELLE Resterilizable Sizers because 2D barcodes may be unreadable by GS-1 scanners due to non-standard formatting.

    Product
    NATRELLE Resterilizable Sizers for the styles and sizes: Style 15, Style 20, Inspira X (responsive gel), Inspira F (responsive gel), Inspira LP (responsive gel), Inspira M (responsive gel), Inspira L (responsive gel), Inspira ST L (Soft Touch gel), Inspira ST LP (Soft Touch Gel),
    Category
    Medical Device
    Distribution
    47 states
  • ModerateNHTSA·19V914000·2019-12-20

    Mercedes-Benz Recalls 2019 GLC Models for Incorrect Air Bag Labels

    Mercedes-Benz is recalling 2019 GLC models because passenger-side sun visors may have air bag warning labels in a foreign language, potentially obscuring safety risks.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLC63S, AMG GLC43, GLC 300, GLC350E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0637-2020·2019-12-18

    AuroMedics Recalls Mirtazapine Tablets Due to Labeling Error

    AuroMedics Pharma LLC is recalling Mirtazapine 15 mg tablets that were incorrectly labeled as 7.5 mg. The error affects 500-count bottles distributed nationwide.

    Product
    MIRTAZAPINE — MIRTAZAPINE (MIRTAZAPINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0334-2020·2019-12-18

    CornFusion Caramel Popcorn Recalled for Undeclared Milk Allergen

    CornFusion Gourmet Popcorn is recalling 12 packages of 7-oz caramel popcorn in Washington because the label declares butter but omits milk.

    Product
    Caramel flavored Popcorn, packaged in poly lined bags, net wt. 7 oz. (198 g). No UPC code.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0662-2020·2019-12-18

    Paragon 28 Recalls Mislabelled Titan 3-D Wedge Implants

    Paragon 28, Inc. is recalling 64 Titan 3-D Wedge implant kits because they are permanently mislabeled with the wrong size, which could cause surgical delays.

    Product
    P28, Titan 3-D Wedge, Evans, Large, 10 mm, sterile, REF P03-EVN-1010-S, Type: Lagrge, Size: 10mm, (01) 00889795018182, Sterile R, Single Use Only
    Category
    Medical Device
    Distribution
    34 states
  • HighFDA (Food)·F-0218-2020·2019-12-18

    Nectar Foods Recalls Honey Mama's Truffle Bar for Unlabeled Milk

    Nectar Foods is recalling Honey Mama's Truffle Bar sold at Trader Joe's because the product contains milk, which is not listed on the label.

    Product
    Honey Mama s Truffle Bar (Trader Joe's) is a honey cocoa bar, refrigerated, one bar is packaged in flexible film, flow wrapped, net weight 1.35 oz. UPC 8 54835 00415 9. There are 12 bars per display case and 6 cases per master case. The label is read in parts: "***Truffle *
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0332-2020·2019-12-18

    CornFusion Maple Bacon Popcorn Recalled for Undeclared Milk Allergen

    CornFusion Gourmet Popcorn is recalling 11 packages of Maple Bacon flavored popcorn because the label declares butter but fails to declare milk.

    Product
    Maple Bacon flavored Popcorn, packaged in poly lined bags, net wt. 7 oz. (198 g). No UPC code.
    Category
    Food
    Distribution
    1 state