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.

3276–3300 of 9607

  • HighFDA (Food)·F-1969-2018·2018-09-26

    CedarLane Organic Couscous Salad Recalled for Undeclared Wheat Allergen

    CedarLane Organic Couscous, Veggies & Chickpeas with Citrus Dressing is being recalled because it is labeled gluten-free but contains undeclared wheat.

    Product
    CedarLane Organic Salads; Couscous, Veggies & Chickpeas with Citrus Dressing. NET WT 9 oz. -Gluten Free -Vegetarian Perishable, Keep Refrigerated. UPC: 38794 99904 Manufactured and Distributed by: CedarLane Foods, Carson, CA 90746
    Category
    Food
    Distribution
    9 states
  • HighFDA (Devices)·Z-3180-2018·2018-09-26

    bioMerieux Recalls VITEK 2 AST-P655 Cards Due to Gentamicin Error

    bioMerieux is recalling VITEK 2 AST-P655 cards because six lots were manufactured with insufficient gentamicin, potentially affecting high-level resistance screening results.

    Product
    VITEK(R) 2 AST-P655, For susceptibility testing of Staphylococcus spp. Enterococcus spp., ad S agalactiae against specified antimicrobials, REF 421913 Product Usage: VITEK¿ 2 is an automated system consisting of instruments, software and reagent cards designed for the identi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3201-2018·2018-09-26

    Medtronic Recalls Contour Plus Link 2.4 Meters with Incorrect Units

    Medtronic is recalling two Contour Plus Link 2.4 meters distributed in Slovakia that display glucose in mg/dL instead of mmol/L.

    Product
    Contour Plus Link 2.4, Product Catalog Number: MMT-1151SK. wireless blood glucose monitoring system Contour Plus LINK 2.4 wireless blood glucose monitoring system (glucometer, test strips and control solution) is designed for self-testing by persons with diabetes and the moni
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-3199-2018·2018-09-26

    Arrow International Recalls PICC Kits Due to Incorrect Catheter Inclusion

    Arrow International is recalling specific PICC kits because they may contain the wrong catheter type, potentially delaying patient treatment.

    Product
    4.5 Fr x 40 cm single-lumen PICC Kit, Product Code CDC-44041-VPS2, 5.5 Fr double-lumen PICC Kit, Product Code CDC-44052-VPS2
    Category
    Medical Device
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-3197-2018·2018-09-26

    Arrow Bipolar Electrode Catheter Recalled for Incorrect Expiration Date Labeling

    Arrow International Inc. is recalling 7 units of a specific bipolar electrode catheter lot because they are labeled with an incorrect expiration date.

    Product
    ARROW¿ Bipolar Electrode Catheter with shrouded pins , 6 Fr, 110 cm Product Code: AI-06210-S Product Usage: Arrow electrophysiology catheters are intended for temporary use in electrophysiology studies for intracardiac stimulation and/or ECG recording
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-3176-2018·2018-09-26

    Zimmer Biomet Recalls Commingled Gentle Thread PLGA Interference Screws

    Zimmer Biomet is recalling 52 Gentle Thread PLGA Round Head Interference Screws because they were commingled with a different screw size.

    Product
    Gentle Thread PLGA Round Head Interference Screw, 7x20mm, Item Number 905612
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-3198-2018·2018-09-26

    Biocare Medical Recalls URO-3 Triple Stain Kits Due to Component Mislabeling

    Biocare Medical is recalling 11 URO-3 Triple Stain kits because two components were mislabeled, causing incorrect staining patterns in laboratory tests.

    Product
    URO-3 Triple Stain (CD44 + p53) with CK20, Catalog #: PM370TSAA, Package Type: Bag, which contains components: a) CD44 + p53, Catalog #: PM373DSAA, Package Type: Bottle, and b) CK20, Catalog #: PM062AA, Package Type: Bottle Product Usage: URO-3 Triple Stain (CD44 + p53) with
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3200-2018·2018-09-26

    Arrow International Recalls PICC Kits Due to Incorrect Catheter Type

    Arrow International is recalling 5.5 Fr x 5.5 Fr x 40 cm double-lumen PICC Kits because they may contain the wrong catheter type, potentially delaying treatment.

    Product
    5.5 Fr x 40 cm double-lumen PICC Kit, Product Code CDC-44052-VPS2
    Category
    Medical Device
    Distribution
    14 states
  • LowFDA (Food)·F-1970-2018·2018-09-26

    Stewart's Ice Cream Recalled for Incorrect Lid Packaging

    Stewart's Shops Corp. is recalling 5,455 pints of Caramel Cone Crunch ice cream because some containers were packaged with the wrong lid.

    Product
    Stewart's Ice Cream Caramel Cone Crunch Carton, 1 pint, keep frozen, UPC: 082086444718
    Category
    Food
    Distribution
    2 states
  • LowFDA (Devices)·Z-3196-2018·2018-09-26

    Smiths Medical Recalls Mislabeled Arterial Blood Sampling Kits

    Smiths Medical ASD Inc. is recalling 29,600 Portex Pulsator Arterial Blood Sampling Kits because they were mislabeled with incorrect labels.

    Product
    Portex Pulsator Arterial Blood Sampling Kit with Dry Lithium Heparin for Gases and Electrolytes, REF 4080P-2, Sterile, RX. The firm name on the label is Smiths Medical ASD, Inc., Keene, NH.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0003-2019·2018-09-19

    H & C Food Inc. Recalls Fish Balls for Undeclared Allergens

    H & C Food Inc. is recalling 14-ounce bags of fish balls because they contain undeclared egg and crustacean allergens.

    Product
    Fish Balls, packaged in a red and white plastic bag with gold font, NET WT: 14OZ (400g), UPC: 6 953006 4 50093. Keep Frozen.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0004-2019·2018-09-19

    Fuzhou Fish Balls Recalled for Undeclared Allergens

    H & C Food Inc. is recalling Fuzhou Fish Balls because they contain undeclared egg, crustacean, and pork.

    Product
    Fuzhou Fish Balls, packaged in a blue and white package bag, in two sizes: Net WT: 14 OZ (400g), UPC: 6 953640 05000 and Net WT:4.5 lbs. (2043g), UPC: 6 953640 050017. Keep Frozen.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-3042-2018·2018-09-19

    LeMaitre AnastoClip GC Closure System Recalled for Incorrect Instructions

    LeMaitre Vascular is recalling AnastoClip GC Closure Systems because the included instructions listed uses not cleared by the FDA.

    Product
    AnastoClip GC Closure System, REF# 4007-08 a closure system designed to penetrate the outer layers of tissue during the forming of an anastomosis or closing of a vessel with possible intraluminal penetration.
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-3026-2018·2018-09-19

    Vascular Technology Recalls 10 Mislabeled 8 MHz Surgical Doppler Transceivers

    Vascular Technology, Inc. is recalling 10 surgical Doppler transceivers that may be mislabeled as 20 MHz units instead of 8 MHz units.

    Product
    VTI 8 MHz Surgical Doppler Transceiver Selectabable Channel Ref. Number: 108910 Intraoperative (microvascular and vascular), Intraoperative Neurological, Transesophageal, Transrectal, Laparoscopic and Peripheral Vascular.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-3039-2018·2018-09-19

    SPS Sterilization Recalls Resterilized Boston Scientific Wallstent RP Endoprosthesis

    SPS Sterilization is recalling two units of resterilized Boston Scientific Wallstent RP Endoprosthesis because the labeling expiration date exceeds the validated shelf life.

    Product
    Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial Transhepatic Biliary Self-Expanding Stent, 8MM X 80MM | 75CM, resterilized.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-3032-2018·2018-09-19

    SPS Sterilization Recalls Edwards Femoral Venous Cannula Due to Shelf Life Error

    SPS Sterilization is recalling one unit of an Edwards Lifesciences Femoral Venous Cannula because the expiration date on the label exceeds the validated shelf life.

    Product
    Edwards Lifesciences Femoral Venous Cannula, 18FR, resterilized.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-3031-2018·2018-09-19

    SPS Sterilization Recalls Avid Venous Drainage Cannulas Due to Shelf Life Labeling

    SPS Sterilization is recalling 5 units of Avid Dual Stage Venous Drainage Cannulas because the expiration date on the label exceeds the validated shelf life.

    Product
    Edwards Lifesciences Avid Dual Stage Venous Drainage Cannula, 29/37F (9.6/12.3MM) X 37CM (14.5"), resterilized.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-3040-2018·2018-09-19

    SPS Sterilization Recalls Boston Scientific Wallstent RP Endoprosthesis Due to Labeling Error

    SPS Sterilization, Inc. is recalling three Boston Scientific Wallstent RP Endoprosthesis tracheobronchial stents because the expiration date on the labeling exceeds the validated shelf life.

    Product
    Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial Self-Expanding Stent, 10MM X 94MM | 135CM, resterilized.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-3035-2018·2018-09-19

    SPS Sterilization Recalls Boston Scientific Wallstent Due to Expiration Date Error

    SPS Sterilization is recalling two Boston Scientific Wallstent devices because the expiration date on the label exceeds the validated shelf life.

    Product
    Boston Scientific Wallstent Endoprosthesis Tracheobronchial Transhepatic Biliary Self-Expanding Stent, 12MM X 90MM | 75CM L, resterilized.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-3038-2018·2018-09-19

    SPS Sterilization Recalls Resterilized Boston Scientific Wallstent Enteral Endoprosthesis

    SPS Sterilization, Inc. is recalling two units of resterilized Boston Scientific Wallstent Enteral Endoprosthesis because the expiration date on the labeling exceeds the validated shelf life.

    Product
    Boston Scientific Wallstent Enteral Endoprosthesis Colonic/Duodenal Stent, 22MM X 90MM, resterilized.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-3028-2018·2018-09-19

    SPS Sterilization Recalls Edwards Lifesciences Aortic Cannula Due to Labeling Error

    SPS Sterilization is recalling 6 units of Edwards Lifesciences EZ Glide Aortic Cannulas because the expiration date on the label exceeds the validated shelf life.

    Product
    Edwards Lifesciences EZ Glide Aortic Cannula, 24F x 37.6CM, resterilized.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-3036-2018·2018-09-19

    SPS Sterilization Recalls Boston Scientific Wallstent Tracheobronchial Stents

    SPS Sterilization is recalling two Boston Scientific Wallstent tracheobronchial stents because the expiration date on the labeling exceeds the validated shelf life of the sterilization process.

    Product
    Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding Stent, 22MM X 45MM | 75CM L, resterilized.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-3037-2018·2018-09-19

    Recall of Boston Scientific Tracheobronchial Stents Due to Sterilization Labeling Error

    SPS Sterilization, Inc. is recalling two Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding Stents because the expiration date on the labeling exceeds the validated shelf life.

    Product
    Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding Stent, 24MM X 70MM | 75CM L, resterilized.
    Category
    Medical Device
    Distribution
    8 states