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.

3651–3675 of 9607

  • ModerateFDA (Devices)·Z-1583-2018·2018-05-09

    DeRoyal SURGI MATE Electrosurgical Pencils Recalled for Sterility Labeling Error

    DeRoyal Industries is recalling 1,800 non-sterile electrosurgical pencils that were incorrectly labeled as sterile. The affected units were distributed to Honduras, Belgium, and The Netherlands.

    Product
    DeRoyal(R) SURGI MATE(R) Electrosurgical Pencil, Button Switch, with 15 ft (4.6 m) Cord and Holster, REF 88-001502 Product Usage: general surgical
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1598-2018·2018-05-09

    Stryker 6376 M-1 Cot Fastener Recalled for Missing Manual Warnings

    Stryker is recalling 59 M-1 Cot Fasteners distributed to the Netherlands because their operation and maintenance manuals are missing warnings and contain incorrect information.

    Product
    6376 M-1 Cot Fastener, catalog no. 6376000000
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-1146-2018·2018-05-09

    Columbia Gorge Gluten Free Cinnamon Sugar Cookies Recalled for Labeling Error

    Columbia Gorge Gluten Free is recalling Cinnamon Sugar Cookies because the ingredient list declared milk, but the 'Contains' statement only listed Dairy.

    Product
    Cinnamon Sugar Cookie, Brand name Columbia Gorge Gluten Free. Packaged in a plastic bag for wholesale purposes. The product is received frozen and baked in house for individual serving. NO UPC
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1586-2018·2018-05-09

    Siemens Atelia IM 1300 Analyzer Recalled for Reporting Factor Errors

    Siemens Healthcare Diagnostics is recalling Atelia IM 1300 Analyzers because reporting and conversion factors may not apply to all units when connected to a single solution system.

    Product
    Atelia IM 1300 Analyzer for in vitro diagnostic testing of clinical specimens.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1494-2018·2018-05-09

    Beijing Syntech Laser surgical lasers recalled for missing certification label

    Beijing Syntech Laser Co., Ltd is recalling seven Nice Station Light Based Platform surgical lasers because the required laser safety certification label was not affixed to the product.

    Product
    Beijing Syntech Laser Nice Station Light Based Platform surgical lasers
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1545-2018·2018-05-09

    BD MAX DNA MMK Lab Use Recalled for Incorrect Package Insert Volume

    Becton Dickinson is recalling BD MAX DNA MMK Lab Use because the package insert incorrectly lists the diluent volume, which could affect assay results.

    Product
    BD MAX DNA MMK Lab Use, catalog no. 442828
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1615-2018·2018-05-09

    IntroMedic Recalls Miriam Capsule Endoscope System Due to Battery Indicator Error

    IntroMedic Co., Ltd. is recalling 82 units of the Miriam Capsule Endoscope System because the battery indicator may incorrectly display orange when the battery is fully charged.

    Product
    Miriam Capsule Endoscope System. Model MR1100 Product Usage: MiroCam Capsule Endoscope System is intended for visualization of the small bowel mucosa. It may be used as a tool in the detection of abnormalities of the small bowel in adults.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1584-2018·2018-05-09

    CooperSurgical Recalls 5 mm Apple-Hunt Secondary Cannulas Due to Packaging Error

    CooperSurgical, Inc. is recalling 520 units of 5 mm Apple-Hunt Secondary Cannulas because they were packaged with the wrong trocar length type.

    Product
    5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length (5 count); Model Number 900-840 Product Usage: The Apple-Hunt Secondary Cannulas are indicated for use in laparoscopic surgical procedures to provide a pathway for the introduction of endoscopic surgical
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1490-2018·2018-05-09

    Beijing Syntech Laser Trixel 11 CO2 Laser Recalled for Missing Label

    Beijing Syntech Laser Co., Ltd is recalling three Trixel 11 CO2 surgical lasers because the required certification label was not affixed to the products.

    Product
    Beijing Syntech Laser Trixel 11 C02 Laser surgical lasers
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-1544-2018·2018-05-09

    BD MAX DNA MMK Recalled for Incorrect Package Insert Volume Instructions

    Becton Dickinson is recalling BD MAX DNA MMK (SPC) because the package insert lists the wrong volume of diluent, which could affect assay results.

    Product
    BD MAX DNA MMK (SPC) For Laboratory Use, catalog no. 442829
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Food)·F-1127-2018·2018-05-02

    Seabear Recalls Cold Smoked Coho Salmon Lox Due to Salt Deviations

    Seabear Company is recalling 2,080 units of Cold Smoked Wild Coho Salmon Lox due to water phase salt deviations and mislabeled storage instructions.

    Product
    Cold Smoked Wild Coho Salmon Lox , Gerard & Dominique Seafoods brand, Reduced Oxygen Packaging, Net Wt. 3 oz (85g). UPC 7 52047 92635 4. The package label of the Cold Smoked Coho Salmon bears this instructions "***KEEP REFRIGERATED AT OR BELOW 38 F***". The master case lab
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0697-2018·2018-05-02

    Bayer Recalls Alka-Seltzer Plus Packages Due to Ingredient Label Mismatch

    Bayer is recalling specific Alka-Seltzer Plus packages because the ingredients listed on the front sticker may not match the actual product inside the carton.

    Product
    All Alka-Seltzer Plus¿ packages with a full front panel instant Redeemable Coupon (IRC) affixed to the individual carton. The recalled products can be identified by checking the Bayer logo located on the lower left corner of the front of the carton. If the logo has an orange or g
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1126-2018·2018-05-02

    Seabear Hot Smoked Keta Salmon Recalled for Salt Deviations and Mislabeling

    Seabear Company is recalling 381 units of Hot Smoked Keta Beergarden Salmon due to water phase salt deviations and mislabeled storage instructions.

    Product
    Hot Smoked Keta Beergarden Salmon, Seabear brand, Reduced Oxygen Packaging, Net Wt. 4oz (113g). No UPC.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1131-2018·2018-05-02

    Frozen Parotta Recalled for Undeclared Milk Allergen

    Maharaja Food Importers is recalling frozen Parotta products because the label lists ghee but fails to declare milk, a major allergen.

    Product
    Parotta Family Pack, UPC: 8 70400 00084 5, Frozen; and Small Parotta, UPC: 870400000012, Frozen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1118-2018·2018-05-02

    Whole Foods Recalls Undeclared Egg Allergen in Iced Easter Cookies

    Whole Foods Market is recalling decorated Easter cookies sold in nine Northern California locations because the signage failed to declare egg as an ingredient and allergen.

    Product
    Decorated (iced holiday cookies sold from self service cookie displays - cookies in the shape of eggs, bunnies and chicks. The signage by the displays do not declare egg as an ingredient of the cookies. Cookies are received in a 9 lb. bag Correct Ingredients: Unbleached, U
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1132-2018·2018-05-02

    MMRF Ela Ada Jaggery Recalled for Undeclared Milk Allergen

    Maharaja Food Importers is recalling frozen MMRF Ela Ada Jaggery because the label lists ghee but fails to declare milk, a major allergen.

    Product
    MMRF Ela Ada Jaggery, UPC: 870400000067, Frozen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1129-2018·2018-05-02

    MMRF Kumbiliappam Recalled for Undeclared Milk Allergen

    Maharaja Food Importers is recalling frozen MMRF Kumbiliappam because the label lists ghee but fails to declare milk as an ingredient.

    Product
    MMRF Kumbiliappam, UPC: 87040000104, Frozen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1130-2018·2018-05-02

    MMRF Neyyappam Recalled for Undeclared Milk Allergen

    Maharaja Food Importers is recalling frozen MMRF Neyyappam because the label lists ghee but fails to declare milk, a major allergen.

    Product
    MMRF Neyyappam, UPC: 870400000111, Frozen
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1525-2018·2018-05-02

    Zimmer GmbH Recalls Avenir Muller Stem Due to Potential Label Mismatch

    Zimmer GmbH is recalling Avenir Muller Stems due to a potential commingle that could result in the product not matching the outer label.

    Product
    Avenir Muller Stem; Item Number: 01.06010.104, Lot Number: 2905496, UDI: (01)00889024479500 (17)220430 (10)2905496
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1512-2018·2018-05-02

    Howmedica Recalls Six Knee Prosthesis Units Due to Incorrect Size Labeling

    Howmedica Osteonics Corp. is recalling six sterile knee prosthesis units because the implant size may not match the box label.

    Product
    Knee Prosthesis, Sterile, Single-Use devices Product Usage: The knee system devices are intended for use in revision total knee arthroplasty to alleviate pain and restore function
    Category
    Medical Device
    Distribution
    0 states