The Recall Desk

Hazard

Mis Labeling recalls

9,622 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,622
Critical
163
Severe
590
Most recent
2026-09-24

Of the 9,622 mis labeling recalls we have scored against our rubric, 163 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 590 (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.

8901–8925 of 9622

  • ModerateFDA (Devices)·Z-0912-2013·2013-03-13

    Atricure Max1 Isolator Transpolar Pen Recalled for Incorrect Labeling

    Atricure Inc. is recalling five Max1 Isolator Transpolar Pens due to incorrect Instructions for Use labeling.

    Product
    Atricure Inc., Max1 Isolator Transpolar Pen. Model A000163. Used to ablate cardiac tissues during cardiac surgery using radiofrequency energy when connected to the AtriCure Ablation and Sensing Unit or for temporary cardiac pacing, sensing, recording, and stimulation during th
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0914-2013·2013-03-13

    Churchill Medical Recalls Lifeguard Infusion Sets Due to Labeling Error

    Churchill Medical Systems is recalling 2,340 Lifeguard Infusion Sets because the labels incorrectly identify the needle gauge and item number.

    Product
    Lifeguard Infusion Set with Smartsite, 20Ga, 1, CLGY-2010 Huber type needle set used for the infusion of medical fluids into implantable ports.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1046-2013·2013-03-13

    Tortilleria Provincia Yellow Corn Tortillas Recalled for Unlabeled Dye

    Tortilleria Provincia is recalling yellow corn tortillas because they contain FD&C Yellow #5, which is not listed on the ingredient label.

    Product
    Yellow Corn Tortillas in 5 lb clear flexible plastic bags with green and yellow printing. Tortilleria Provincia 1200 B Clay Street Bowling Green, KY 42101
    Category
    Food
    Distribution
    1 state
  • LowFDA (Devices)·Z-0917-2013·2013-03-13

    ConMed Linvatec Recalls D3000I Surgical Drive Systems Due to Incorrect Symbology

    ConMed Linvatec is recalling 23 D3000I Advantage Drive Systems because the membrane switch panel contains incorrect symbology, violating IEC60606-01 standards.

    Product
    D3000I Advantage Drive System, 230v, surgical instrument motor. Product Usage: The Advantage Drive Systems function as a powered instrument system consisting of handpieces and accessories to perform cutting of soft tissue and bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0916-2013·2013-03-13

    Linvatec Recalls D3000 Advantage Drive Systems Due to Incorrect Panel Symbology

    Linvatec Corp. is recalling 31 D3000 Advantage Drive Systems because the front panel contains incorrect symbology, violating IEC60606-01 standards.

    Product
    D3000 Advantage Drive System, 115v Product Usage: The Advantage Drive Systems function as a powered instrument system consisting of handpieces and accessories to perform cutting of soft tissue and bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0883-2013·2013-03-06

    Philips GEMINI TF Big Bore PET/CT Systems Recalled for Software Error

    Philips is recalling 37 GEMINI TF Big Bore PET/CT systems because a software error may cause generated Intensity Projection data to be flipped and incorrectly labeled.

    Product
    Philips Medical Systems, GEMINI TF Big Bore, Model #882476, Positron Emission Tomography (PET) and X-Ray Computed Tomography (CT) scanning system, a diagnostic imaging systems for fixed or mobile installations that combines Positron Emission Tomography (PET) and X-ray Computed To
    Category
    Medical Device
    Distribution
    43 states
  • HighFDA (Food)·F-1027-2013·2013-03-06

    GFS Lemon Pudding Recalled for Undeclared Milk Allergen

    Associated Milk Producers, Inc. is recalling GFS Lemon Pudding because the label fails to list milk, an ingredient present in the vanilla pudding component.

    Product
    GFS Lemon Pulling, Net Wt. 113 oz (7 lb 1 oz) 3.20 kg UPC 93901-10676. Distributed by Gordon Food Service, Grand Rapids, MI 49548.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0703-2013·2013-03-06

    GE Healthcare Definium 5000 X-Ray System UI Display Recall

    GE Healthcare is recalling Definium 5000 X-Ray Systems because the user interface may display incorrect exposure settings during rapid protocol switching.

    Product
    GE Healthcare Definium 5000 / 5220493 X-Ray System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1006-2013·2013-03-06

    Whole Foods Market Panettone Chocolate Recalled for Mispackaging

    Whole Foods Market is recalling Panettone Chocolate because some units were mispackaged with Cranberry Panettone, creating a potential soy allergen discrepancy.

    Product
    Whole Foods Market Panettone Chocolate - 26.4 oz, 12 per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0704-2013·2013-03-06

    GE Healthcare Definium 5000 X-Ray System UI Display Recall

    GE Healthcare is recalling Definium 5000 X-Ray systems because the user interface may display incorrect exposure settings during rapid protocol switching.

    Product
    GE Healthcare Definium 5000/5220493-2 X-Ray System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0891-2013·2013-03-06

    Myco Medical Recalls Technocut Plus Safety Scalpels Due to Sterility Concerns

    Myco Medical is recalling Technocut Plus safety scalpels due to labeling errors and defective packaging that may compromise sterility.

    Product
    Technocut Plus, Sterile Single Use Safety Scalpel, Distributed by: Myco Medical.
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-0898-2013·2013-03-06

    MedComp Recalls 785 PICC Kits Packaged with Incorrect Needles

    Medical Components, Inc. is recalling 785 power injectable infusion PICC insertion kits because they were packaged with non-safety needles instead of the safety needles indicated on the label.

    Product
    REF CMS-CT6T225, 6F Triple Lumen CT PICC with M.S.T. Components Product Usage: Power injectable infusion PICC insertion kits
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0886-2013·2013-03-06

    Integra Jarit Monopolar Cable Recall for Updated Safety Warnings

    Integra LifeSciences is recalling 22,500 Jarit Monopolar Cables to distribute an addendum to the Instructions for Use. The update emphasizes existing warnings and adds new precautions for electrosurgical equipment.

    Product
    Integra(R) Jarit(R) Monopolar Cable (Catalogue No. 600-290). For use in endoscopic surgery. For use when a rigid endoscopic instrument for grasping and/or dissecting if soft tissue is determined to be appropriate by the surgeon. Monopolar electrosurgical current can be used
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0876-2013·2013-03-06

    Ultradent Recalls Mislabelled Avex CX Orthodontic Brackets

    Ultradent Products, Inc. is recalling 124 units of Avex CX orthodontic brackets due to incorrect labeling. The affected products were distributed nationwide in the US.

    Product
    Avex CX Suite, Avex CX 0.22 UL4,5 HK REF #224-017, Product Usage: Avex CX ceramic brackets are formed with 99.9% pure alumina oxide. The indicated use of the Avex CX ceramic bracket is the mechanical movement of natural teeth in conjunction with other components designed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-177-2013·2013-03-06

    Bayer Recalls Bronkaid Dual Action Formula Due to Labeling Errors

    Bayer Healthcare is recalling Bronkaid Dual Action Formula caplets because the carton label is missing a warning or Rx legend and other information.

    Product
    Bronkaid Dual Action Formula, Ephedrine Sulfate 25 mg/Bronchodilator, Guaifenesin 400 mg/Expectorant, a) 24 coated caplets per blister pack, UPC 300240537879, b) 60 coated caplets per blister pack, UPC 300240537855, Bayer HealthCare LLC, Consumer Care, P.O. Box 1910, Morristown,
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowNHTSA·13V084000·2013-03-05

    Volvo Recalls 2013 S60 and XC60 for Incorrect Certification Labels

    Volvo is recalling 2013 S60 and XC60 vehicles manufactured on January 7, 2013, because their certification labels list the incorrect manufacture year.

    Product
    VOLVO — VOLVO S60, XC60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0825-2013·2013-02-27

    HealthTronics RenalCryo Cryoprobe Recalled for Incorrect Expiration Label

    Healthtronics, Inc. is recalling 50 units of Endocare 3.8mm RenalCryo Cryoprobes because the outer box labels display incorrect expiration dates.

    Product
    HealthTronics Endocare 3.8mm RenalCryo Cryoprobe, R3.8L. The Endocare CryoProbe is an accessory probe intended for use with the CryoCare Surgical System, for freezing and ablation of tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V063000·2013-02-26

    US Specs Recalls Four Vehicles for Incorrect Passenger Mirror Labels

    US Specs is recalling four vehicles to correct incorrect font size labels on passenger side mirrors, which may hinder drivers' ability to judge object proximity.

    Product
    PORSCHE — PORSCHE, BMW 911 CARRERA, 750IL, 635
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V059000·2013-02-25

    Northwood Recalls 2013 Trailers Due to Incorrect Federal Identification Labels

    Northwood is recalling specific 2013 model year trailers because incorrect information on federal identification and weight labels could lead to improper loading and axle failure.

    Product
    SNOW RIVER — SNOW RIVER, ARTIC FOX, FOX MOUNTAIN 266RDS, 295K, 285RLS, 295T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0973-2013·2013-02-20

    Pizza Mini Turnovers Recalled for Undeclared Milk Allergen

    Suadel Food Products is recalling Estrella Pastelillos de Pizza because the common name 'milk' is not declared in the ingredients or 'Contains' statement.

    Product
    "Estrella Food Products, Inc***Pastelillos de Pizza (Pizza Mini Turnovers)***6 units***Manufactured by: Estrella Food Products, Inc., Minilla Industrial Park, Bayamon, PR 00959-1906***".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0974-2013·2013-02-20

    Suadel Empanadillas Recalled for Undeclared Wheat and Soy Allergens

    Suadel Food Products is recalling Empanadillas Sabor a Carne because wheat and soy are not declared on the label.

    Product
    "Estrella Food Products, Inc***Empanadillas Sabor a Carne(Meat flavorTurnovers)***5 units, 12 units and 24 units***Elaborado y Empacado por: Estrella Food Products, Inc., Bayamon, PR 00959-1906***".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0795-2013·2013-02-20

    Lumenis Recalls VersaCut Tissue Morcellator for Labeling Corrections

    Lumenis Limited is recalling VersaCut Tissue Morcellator devices to correct labeling following three reported air embolism events caused by incorrect tubing hook-up.

    Product
    The Lumenis VersaCut Tissue Morcellator Product Usage: is intended for use under direct or endoscopic visualization for the morcellation and removal of dissected tissue during pelviscopic, laparoscopic, percutaneous, and open surgical procedures whenever access to the surgi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0811-2013·2013-02-20

    Ultradent Chromaclone PVS Impression Material Recalled for Packaging Error

    Ultradent Products is recalling specific lots of Chromaclone PVS impression material due to incorrect packaging of regular and fast set cartridges.

    Product
    Ultradent Products, Chromaclone PVS, Regular Set heavy body, Bubble Gum Flavor, 50 ml, Impression Material, Part No. 5012, Lot No. B7PPC. Used in prosthodontics.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0812-2013·2013-02-20

    Ultradent Chromaclone PVS Impression Material Recalled for Packaging Error

    Ultradent Products is recalling specific lots of Chromaclone PVS impression material due to incorrect packaging of regular and fast set cartridges.

    Product
    Ultradent Products, Chromaclone PVS, Fast Set heavy body, Bubble Gum Flavor, 50 ml, Impression Material, Part No. 5013, Lot No. B7DS3, Used in prosthodontics.
    Category
    Medical Device
    Distribution
    Distributed nationwide