The Recall Desk

Hazard

Mis Labeling recalls

9,610 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,610
Critical
161
Severe
588
Most recent
2026-09-16

Of the 9,610 mis labeling recalls we have scored against our rubric, 161 (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.

5751–5775 of 9610

  • HighFDA (Food)·F-1074-2016·2016-04-20

    Hidden Valley Original Ranch Dressing Recalled for Missing Soy Label

    The Clorox Company is recalling Hidden Valley Original Ranch dressing because some bottles are missing the soy lecithin ingredient declaration.

    Product
    Hidden Valley Original Ranch dressing, 16 fl oz. ( 473 ml). plastic bottles; Ingredients: Vegetable oil (soybean and/or Canola oil) water, egg yolk, sugar, Salt, Cultured non fat buttermilk, natural flavors (milk, soy), less than 1% spiced, dried garlic, dried onion, vinegar,
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1026-2016·2016-04-20

    Gold Medal Cincinnati Style Chili Recalled for Undeclared Milk

    Gold Medal Products is recalling 4 lb jars of Cincinnati Style Chili because the label failed to declare milk as an ingredient.

    Product
    #2473 CINCINNATI STYLE CHILI Savory Net Wt. 4 lbs (1.8kg) UPC 0 90939 12473 1 GOLD MEDAL PRODUCTS 10700 MEDALLION DRIVE CINCINNATI, OHIO 45241
    Category
    Food
    Distribution
    16 states
  • HighFDA (Food)·F-1047-2016·2016-04-20

    Figi's Classic Marzipan Recalled for Unlabeled Almond Content

    Figi's is recalling 8-ounce packages of Classic Marzipan because the product contains almonds that are not properly labeled on the ingredients list.

    Product
    Figi's Classic Marzipan, item 100-0034-200, 8 ounce
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1046-2016·2016-04-20

    Kroger Chicken Salad Croissant Sandwiches Recalled for Undeclared Fish

    Mt Perry Foods is recalling Kroger Brand Chicken Salad Croissant Sandwiches sold in Ohio and West Virginia because they contain undeclared fish.

    Product
    Kroger Brand Chicken Salad Croissant Sandwiches packaged in individual clear rigid plastic clamshell containers packaged in 6 brown corrugated card board boxes, 6 to a case, for a total of 36 sandwiches. Cases identified with white stick on label with black ink printing reading
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1392-2016·2016-04-20

    Synthes OPAL Spinal Fusion Cage Recalled for Labeling Mismatch

    Synthes (USA) Products LLC is recalling 6 units of OPAL Spacers because the outer packaging label does not match the product inside or its intended use.

    Product
    Oblique Posterior Atraumatic Lumbar (OPAL) System, Polymeric spinal fusion cage, non-sterile, OPAL Spacer 10 mm x 24 mm, 11 mm Height - Revolve Product Usage - The OPAL Spacer is indicated for use in patients with degenerative disc disease (DDD) at one or two contiguous levels
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1370-2016·2016-04-20

    Boston Scientific Recalls PT Graphix Magnet J-TIP Guidewires Due to Tip Defect

    Boston Scientific is voluntarily recalling PT Graphix Magnet J-TIP Guidewires because the wires are straight instead of having the pre-formed J-tip.

    Product
    Boston Scientific, PT Graphix Magnet J-TIP Guidewire with ICE Hydrophilic Coating, Sterile EO, UPN H7491490201MJ2 (Carton Label) ,H7491490201MJo (UPN referenced on the Pouch Label) . Boston Scientific PT Graphix Magnet Guidewire with ICE Hydrophilic Coating is a steerable gui
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0819-2016·2016-04-20

    Fresenius Kabi Recalls Cisatracurium Vials Due to Labeling Error

    Fresenius Kabi is recalling 94,560 vials of Cisatracurium Besylate Injection because the carton labels incorrectly state the product is preservative-free.

    Product
    CISATRACURIUM — CISATRACURIUM (CISATRACURIUM BESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1497-2016·2016-04-20

    AMT G-Jet Feeding Device Recalled for Length Discrepancy

    Applied Medical Technology is recalling 20 units of G-Jet feeding devices because they are shorter than labeled.

    Product
    AMT G-Jet¿ Low-Profile Transgastric-Jejunal Feeding Device 14F 1.5cm 45cm SINGLE USE ONLY Rx ONLY STERILE. For use in patients who cannot absorb adequate nutrition through the stomach.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1357-2016·2016-04-20

    Bard Foley Catheter Recalled for Incorrect Inflation Volume Labeling

    C.R. Bard is recalling 1.4 million Bardex Foley catheters because the instructions for use list an incorrect inflation volume.

    Product
    BARDEX I.C. Anti-Infective 2-Way 3cc Foley Catheter, Rx only. Intended for urinary bladder drainage in female patients requiring catheterization for management of incontinence, voiding dysfunction and surgical procedure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1359-2016·2016-04-20

    C.R. Bard Recalls Foley Catheters Due to Labeling Error

    C.R. Bard is recalling 1.4 million latex Foley catheters because the instructions for use list an incorrect inflation volume.

    Product
    BARDEX I.C. Anti-Infective 2-Way Red Latex Foley Catheter, 5cc (Council Model); Intended for urinary bladder drainage in female patients requiring catheterization for management of incontinence, voiding dysfunction and surgical procedure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1375-2016·2016-04-20

    Merit Medical Recalls TSX Transseptal Needle Due to Labeling Error

    Merit Medical Systems is recalling one lot of TSX Transseptal Needles because the packaging labels incorrectly state a 50-degree curve instead of the actual 86-degree curve.

    Product
    Boston Scientific TSX Transseptal Needle, Model Number M004TSX60o; Used to create the primary puncture in the interatrial septum when passing an intruder and/or catheter through the septum from the right side of the heart to the left side.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1358-2016·2016-04-20

    Bard Foley Catheter Recall Due to Incorrect Inflation Volume Labeling

    C.R. Bard is recalling 1.4 million Bardex Foley catheters because the instructions for use list an incorrect inflation volume.

    Product
    BARDEX I.C. Anti-Infective 2-Way 5cc Foley Catheter. Intended for urinary bladder drainage in female patients requiring catheterization for management of incontinence, voiding dysfunction and surgical procedure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1070-2016·2016-04-20

    Gutierrez Distributors Recalls Tamarind Products for Undeclared Red Dye

    Gutierrez Distributors is recalling two tamarind products in New Jersey due to undeclared FD&C Red 40.

    Product
    Gutierrez Distributor, (a) Tarugo con chile spicy tamarind, 349 Chestnut Street, Passaic, NJ 07055 UPC 8527050000904 (b) Dulce de pulpa 100% de Tamarindo, Betamex, Alamos No.7 STA. Maria Aztahuacan Deleg. Iztapalapa C.P. 09500 Mexico, D.F.
    Category
    Food
    Distribution
    1 state
  • LowFDA (Devices)·Z-1390-2016·2016-04-20

    BD Retic-Count Reagent System Recalled for Incorrect Storage Labeling

    Becton, Dickinson and Company is recalling one lot of BD Retic-Count Reticulocyte Reagent System because the carton label listed incorrect storage conditions.

    Product
    BD-Retic-Count Reticulocyte Reagent System; Hematology: Used for in vitro diagnostics
    Category
    Medical Device
    Distribution
    10 states
  • LowFDA (Drugs)·D-0820-2016·2016-04-20

    Impax Recalls Fenofibrate Capsules Due to Incorrect or Missing Labeling

    Impax Laboratories is recalling 28,001 bottles of Fenofibrate Capsules (Micronized) 134 mg because the bottles have incorrect or missing lot and expiration dates.

    Product
    Fenofibrate Capsules (Micronized) 134 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA 94544, NDC 0115-0522-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0823-2016·2016-04-20

    Amerisource Recalls Fenofibrate Capsules Due to Incorrect or Missing Labeling

    Amerisource Health Services is recalling 5,034 cartons of Fenofibrate Capsules (Micronized), 200 mg, due to incorrect or missing lot and expiration dates.

    Product
    Fenofibrate Capsules (Micronized), 200 mg , 30-count Unit Dose Blister Packs per carton, Rx Only, Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217 Carton of 30:NDC 68084-835-32, Individual Dose: NDC 68084-835-33.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0821-2016·2016-04-20

    Impax Recalls Fenofibrate Capsules Due to Incorrect or Missing Labeling

    Impax Laboratories is recalling 42,239 bottles of Fenofibrate Capsules (Micronized) 200 mg because some bottles have incorrect or missing lot and expiration dates.

    Product
    Fenofibrate Capsules (Micronized) 200 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA 94544, NDC 0115-0533-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0822-2016·2016-04-20

    Amerisource Health Services Recalls Fenofibrate Capsules Due to Labeling Errors

    Amerisource Health Services is recalling 228 cartons of Fenofibrate Capsules because some units have incorrect or missing lot and expiration dates.

    Product
    Fenofibrate Capsules (Micronized), 134 mg Capsules, 20-count Unit Dose Blister Packs per carton, Rx Only, Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217, Carton of 20: NDC 68084-835-32, Individual Dose: NDC 68084-835-33.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·16V217000·2016-04-14

    Glaval Bus Transit Models Recalled for Emergency Exit Label Placement

    Forest River is recalling 2008-2016 Glaval Bus transit models because rear emergency exit labels are not placed within 16 centimeters of release mechanisms, potentially hindering quick escape.

    Product
    GLAVAL BUS — GLAVAL BUS TITAN II, APOLLO, TITAN II LOW FLOOR, TITAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1016-2016·2016-04-13

    Immuno-Dynamics Recalls PerCoBa Colostrum Supplement for Missing Milk Labeling

    Immuno-Dynamics is recalling PerCoBa and Synertek colostrum supplements because the labels fail to state that the products contain milk.

    Product
    PerCoBa 1, Colostral Whey, Dietary Supplement, Colostral Whey Protein 6.4%. Net Contents: 4 oz. Immuno-Dynamics, Inc. , PO Box 544 Perry, Iowa 50220
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1017-2016·2016-04-13

    PerCoBa Whey Protein Isolate Recalled for Missing Milk Allergen Labeling

    Immuno-Dynamics, Inc. is recalling PerCoBa Whey Protein Isolate with Colostrum because the labels fail to state that the product contains milk.

    Product
    PerCoBa Whey Protein Isolate with Colostrum, Dietary Supplement. Net Weight: 1 kg (2.2 lbs), Colostrum 3,000 mg. UPC 90576-00009. Immuno-Dynamics, Inc., 18000 Dodge Street, Fennimore, WI 53809.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1021-2016·2016-04-13

    YumEarth Gummy Bears Recalled for Carbohydrate Labeling Error

    Yummy Earth Inc. is recalling YumEarth Organics Gummy Bears due to inconsistent carbohydrate labeling on the packaging.

    Product
    YumEarth Organics Gummy Bears 5 oz. Distributed by YummyEarth Inc., Ramsey, NJ 07446 UPC 810165018310
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1340-2016·2016-04-13

    Zimmer Persona Knee Implant Recalled for Box Labeling Discrepancy

    Zimmer Manufacturing B.V. is recalling specific Persona knee implants because the product information on the box differed by sides, showing conflicting part and lot numbers.

    Product
    Persona The Personalized Knee System Articular Surface Posterior Stabilized (PS) Left Height 14mm Sterile. For use in total knee arthroplasty. REF 42-5114-005-14
    Category
    Medical Device
    Distribution
    19 states
  • ModerateFDA (Food)·F-1015-2016·2016-04-13

    Immuno-Dynamics Recalls Colostrum Lozenges for Allergen Labeling Error

    Immuno-Dynamics, Inc. is recalling PerCoBa and Synertek colostrum lozenges because the labels state 'contains dairy' instead of 'contains milk.'

    Product
    Colostrum Lozenges, Dietary Supplement, Colostrum (Bovine) 200mg. Allergen statement: contains dairy. Packaged in the following sizes and Brand names: 1. PerCoBa, UPC 90576-00006. 100 Lozenges Distributed by: Immuno-Dynamics, Inc., Fennimore, WI 53809; 2. Syner
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1341-2016·2016-04-13

    Zimmer Persona Knee Implant Recalled for Box Labeling Discrepancy

    Zimmer Manufacturing B.V. is recalling specific Persona knee implants because the product box displayed conflicting part and lot numbers on different sides.

    Product
    Persona The Personalized Knee System Articular Surface Posterior Stabilized (PS) Left Height 18mm Sterile For use in total knee arthroplasty. REF 42-5114-008-18
    Category
    Medical Device
    Distribution
    19 states