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.

4801–4825 of 9607

  • HighFDA (Food)·F-1789-2017·2017-04-05

    Kusher LLC Recalls Shishka Cookies Due to Allergen Labeling Error

    Kusher LLC is recalling Shishka Cookies because the packaging failed to list egg and milk in the 'Contains' statement, despite listing them in the ingredients.

    Product
    COOKIES SHISHKA, product is packaged in plastic clamshells container, Net Weight: 454g (16 OZ), UPC: 8 51929 00362 3. The label is read in parts: "***COOKIES "SHISHKA" *** INGREDIENTS: WHEAT FLOUR (FLOUR, NIACIN, IRON, THIAMINE MONONITRATE, RIBOFLAVIN, FOLIC ACID) ASCORBIC A
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1701-2017·2017-04-05

    Biomet 3i Recalls Dental Implants Due to Potential Label Mismatch

    Biomet 3i is recalling five units of LTX dental implants because a single part in the lot may not match the label due to a supplier error.

    Product
    BIOMET 3i LTX DENTAL IMPLANTS Model LTX610 (6x10mm) - Plastic tray within Tyvek tray within cardboard box; one (1) unit per box. Labeled Sterile"
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·17V218000·2017-03-31

    Forest River Recalls 2017 Salem and Wildwood RVs for Incorrect Weight Labels

    Forest River is recalling 2017 Salem and Wildwood recreational vehicles because the Federal Placard lists an incorrect Gross Axle Weight Rating, which could lead to overloading.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1485-2017·2017-03-29

    PureWick External Catheter Recalled for Latex Labeling Errors

    Purewick Corporation is recalling 176,863 units of the PureWick External Catheter for Women because the labeling failed to disclose the presence of dry natural rubber and incorrectly stated the product was latex-free.

    Product
    PureWick External Catheter for Women-Wick Product Usage: A flexible, contoured external catheter (a Wick) is positioned between the labia and gluteus muscles. The function of the Wick is to draw urine away from the body through the Wick to a storage container away from the b
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1517-2017·2017-03-29

    Merge Healthcare Recalls Merge Cardio Software Due to Data Integrity Issues

    Merge Healthcare is recalling Merge Cardio software versions 9.0 through 9.0.8 because users can merge device files with confirmed reports, potentially adding unverified information.

    Product
    Merge Cardio software. Product Usage: Merge Cardio is a system intended to be used to acquire, store, print, transfer, and archive clinical information including images, Hemodynamic studies and reports, measurements (via import from DICOM Structured Reporting, text files or
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1628-2017·2017-03-29

    Dito's Strawberry Platters Recalled for Undeclared Milk and Soy

    Dito's is recalling refrigerated strawberry platters with chocolate frosting due to undeclared milk and soy allergens.

    Product
    Ditos Heart shaped plastic Platter of Strawberries with Dip of Chocolate Frosting- Refrigerated. Net wt. 32 oz. UPC 8 93268 00142 7. The label is read in parts: "***Heart Platter Strawberries w/ Dip***32 oz.*** Strawberries USA (dip)***by Dito's LLC, Anchorage, AK 99518***".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1670-2017·2017-03-29

    Carriage House Creations Recalls Bourbon Basting Sauce for Undeclared Allergens

    Carriage House Creations is recalling specific varieties of Bourbon Basting Sauce and Hot BBQ Sauce due to undeclared peanuts and soy.

    Product
    Carriage House Creations; Bourbon Basting Sauce Hot; Net wt. 12 Ounces; Carriage House Creations, 544 Gordon Alley; Reynoldsville, PA 15851;
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1492-2017·2017-03-29

    Philips CT Scanner Recall for Incorrect 4D CT Image Phase Annotations

    Philips is recalling 11 Brilliance BigBore Oncology CT scanners because retrospective 4D CT scans may display incorrect phase annotations.

    Product
    Brilliance BigBore Oncology CT - 728243 Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and display equi
    Category
    Medical Device
    Distribution
    22 states
  • ModerateFDA (Devices)·Z-1487-2017·2017-03-29

    Crossroads MotoCLIP Super Elastic Fusion System Recalled for Incorrect Sizing

    Crossroads Extremity Systems is recalling 20 units of MotoCLIP Super Elastic Fusion Systems because seven implants were incorrectly sized and labeled.

    Product
    MotoCLIP(TM) Super Elastic Fusion System, Size 18mm x 14mm x 14mm, REF 1442-1814, Rx Only, STERILE R.
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Drugs)·D-0612-2017·2017-03-29

    Fougera Recalls Desonide Ointment Tubes Due to Labeling Mixup

    Fougera Pharmaceuticals is recalling 14,665 tubes of Desonide Ointment because unit boxes may contain tubes labeled as Ketoconazole Cream.

    Product
    Desonide Ointment, 0.05%, NET WT 60 grams tubes, Rx only, E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc., Melville, New York 11747, NDC 0168-0309-60
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1512-2017·2017-03-29

    Devicor Mammotome Revolve Biopsy System Recalled for Missing Labeling

    Devicor Medical Products Inc is recalling 320 Mammotome Revolve Dual Vacuum Assist Biopsy Systems because they lack required probe labeling, product codes, and sterilization stickers.

    Product
    Mammotome Revolve Dual Vacuum Assist Biopsy System The device is used to sample breast tissue that has been identified as suspicious under imaging guidance
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Drugs)·D-0604-2017·2017-03-29

    Bayer Recalls A+D Diaper Rash Cream Due to Labeling Error

    Bayer HealthCare Pharmaceuticals is recalling A+D Diaper Rash Cream due to a labeling claim issue regarding undeclared excipients.

    Product
    A+D Diaper Rash Cream with Dimethicone 1% and Zinc Oxide 10%, Packaged in a) 1.5 oz (42.5g) ( UPC 041100811288), b) 3 oz 85g (UPC 041100811301), c) 4 oz (113g) (UPC 041100811325), Distributed by: Bayer Healthcare LLC, Whippany, NJ 07981
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1493-2017·2017-03-29

    Philips Recalls Brilliance BigBore CT Scanners Due to Image Reconstruction Error

    Philips is recalling 67 Brilliance BigBore CT scanners because 4D CT images may be reconstructed at a single phase while incorrectly labeled as specific phases.

    Product
    Brilliance BigBore Radiology CT - 728244 Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and display equ
    Category
    Medical Device
    Distribution
    22 states
  • ModerateFDA (Devices)·Z-1484-2017·2017-03-29

    FDA Recalls Microbore Extension Sets Due to Incorrect Priming Volume Labeling

    Vygon MFG is recalling 30,700 AMS-636 Microbore extension sets because the package displays an incorrect priming volume.

    Product
    AMS-636, 60" Microbore extension set. Product Usage: Accessory devices used to administer medical fluids.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1536-2017·2017-03-29

    MedComp Recalls 9.6F CT Ports with Incorrect Introducer Size

    Medical Components, Inc. is recalling 71 units of 9.6F CT Ports because they were packaged with 9F introducers instead of the labeled 10F size, preventing proper insertion.

    Product
    9.6F Plastic Dignity Mid-Sized CT Port w/Pre-Attached Silicone Catheter The CT Power Injectable Implantable Infusion Ports are indicated for patient therapies requiring repeated access to the vascular system. The port system can be used for infusion of medications, I.V. fluids,
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Food)·F-1638-2017·2017-03-29

    Jugos La Morovena Lemon Juice Recalled for Missing Phenylalanine Warning

    Jugos y Agua La Morovena Inc. is recalling lemon juice in Puerto Rico because the labels lack the required warning for people with phenylketonuria.

    Product
    Jugos La Morove¿a, Lim¿n (Lemon) ,Elaborado y Envasado por Jugos La Morove¿a, Carr 634 km 5.1, Bo. Franquez, Morovis PR 00687
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1500-2017·2017-03-29

    Haag-Streit EyeSuite Software Recalled for Potential Patient Data Misattribution

    Haag-Streit USA Inc is recalling EyeSuite i.8.2.1.0 software due to a risk that patient data may be stored under the wrong patient on the DICOM Server.

    Product
    EyeSuite i.8.2.1.0 Software for ophthalmic use including selection of Intra Ocular Lenses (IOLs).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1535-2017·2017-03-29

    Tearscience LipiFlow System Recalled for Inconsistent Storage Temperature Labeling

    Tearscience is recalling LipiFlow Thermal Pulsation Systems because the labeled storage temperature does not match tested conditions for the full shelf life.

    Product
    LipiFlow Thermal Pulsation System/LipiFlow, System Activator (Disposable), Rx Only, Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1528-2017·2017-03-29

    BioMerieux Recalls ETEST Fosfomycin Strips Due to Unsupported Shelf-Life Claims

    BioMerieux SA is recalling ETEST Fosfomycin FM1024 strips because internal testing does not support the current shelf-life claims.

    Product
    ETEST Fosfomycin FM1024 Blister packaging, Product Name: ETEST Fosfomycin FM 0.064-1024. ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae, Pseudomonas, Staphylococcus
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1523-2017·2017-03-29

    BioMerieux Recalls ETEST Ceftriaxone Strips Due to Stability Issues

    BioMerieux SA is recalling ETEST Ceftriaxone antimicrobial susceptibility testing strips because their shelf-life claims are not supported by internal testing.

    Product
    ETEST¿ Ceftriaxone TXL32 SPB, Product Name: ETEST¿ Ceftriaxone TX 0.002-32(low). ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae, Pseudomonas, Staphylococcus and Ent
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1519-2017·2017-03-29

    Teleflex Recalls Non-Latex Nasopharyngeal Airways Due to Labeling Error

    Teleflex Medical is recalling 7,600 units of Green Non-Latex Robertazzi Nasopharyngeal Airways due to a labeling error. The voluntary recall covers products distributed in the US, Canada, and Mexico.

    Product
    Teleflex Green Non-Latex Robertazzi Nasopharyngeal Airway, Catalog No. 123130 and 123132 Product Usage: To provide a patent airway for a patient with a blockage or potential blockage of the nasal cavity or nasopharynx.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1527-2017·2017-03-29

    BioMerieux Recalls Etest Benzyl Penicillin Strips Due to Stability Issues

    BioMerieux SA is recalling Etest Benzyl Penicillin PG256 FOAM packaging because shelf-life claims are not supported by internal testing.

    Product
    ETEST Benzyl Penicillin PG256 FOAM packaging, Product Name: Etest Benzylpenicillin PG 0.016-256 (high). ETEST is a quantitative technique for determining the antimicrobial susceptibility of Gram-negative and Gram-positive aerobic bacteria such as Enterobacteriaceae, Pseudomonas,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1632-2017·2017-03-29

    Jugos La Morovena Grapefruit Juice Recalled for Missing Phenylalanine Warning

    Jugos y Agua La Morovena Inc. is recalling 195 gallons of grapefruit juice in Puerto Rico because the labels lack the required phenylalanine warning for individuals with phenylketonuria.

    Product
    Jugos La Morove¿a, Toronja (Grapefruit),Elaborado y Envasado por Jugos La Morove¿a, Carr 634 km 5.1, Bo. Franquez, Morovis PR 00687
    Category
    Food
    Distribution
    1 state
  • LowFDA (Food)·F-1633-2017·2017-03-29

    Jugos La Morovena Grape Juice Recalled for Missing Phenylketonuria Warning

    Jugos y Agua La Morovena Inc. is recalling 106 gallons of grape juice in Puerto Rico because the labels lack the required phenylketonuria warning.

    Product
    Jugos La Morove¿a, Uva (Grape),Elaborado y Envasado por Jugos La Morove¿a, Carr 634 km 5.1, Bo. Franquez, Morovis PR 00687
    Category
    Food
    Distribution
    1 state
  • LowFDA (Food)·F-1631-2017·2017-03-29

    Jugos La Morovena Orange Juice Recalled for Missing Phenylketonuria Warning

    Jugos y Agua La Morovena Inc. is recalling 309 gallons of orange juice in Puerto Rico because the labels lack the required phenylalanine warning for people with phenylketonuria.

    Product
    Jugos La Morove¿a, China (Orange),Elaborado y Envasado por Jugos La Morove¿a, Carr 634 km 5.1, Bo. Franquez, Morovis PR 00687
    Category
    Food
    Distribution
    1 state