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.

Which agencies issued them

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.

6226–6250 of 9610

  • LowFDA (Devices)·Z-2432-2015·2015-08-26

    Cepheid Recalls Xpert CT/NG Urine Specimen Collection Kits

    Cepheid is recalling Xpert CT/NG Urine Specimen Collection Kits because some lots contain a sub-component with an expiration date earlier than the kit's expiration date.

    Product
    Xpert CT/NG Urine Specimen Collection Kit Part number GXCT/NGURINE-50; Microbiology: Xpert CT/NG Urine Specimen Collection Kit is designed to preserve and transport Chlamydia trachomatis and Neisseria gonorrhoeae DNA in first-catch male and female urine specimens from symptom
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1350-2015·2015-08-26

    Qualitest Recalls Ampicillin Capsules Due to Unapproved Labeling

    Vintage Pharmaceuticals LLC is recalling 360 bottles of Ampicillin Capsules, USP, 250 mg, because they are labeled with unapproved labeling.

    Product
    AMPICILLIN CAPSULES, USP, 250 mg, 500 count bottles, Rx only, Manufactured for: DAVA Pharmaceuticals, Inc., Fort Lee, NJ, By: Suir Pharma Ireland Ltd., Clonmel, Ireland, NDC: 67253-180-50
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Food)·F-2952-2015·2015-08-19

    D & D Foods Recalls Dijon Mustard Potato Salad for Allergen Mislabeling

    D & D Foods is recalling 110 cases of Dijon Mustard Potato Salad sold in Hy-Vee stores because the product contains milk and wheat but fails to disclose these allergens.

    Product
    Dijon Mustard Potato Salad, NET WT 3 LB (1.36 kg)
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-2957-2015·2015-08-19

    ASN Dietary Supplements Recalled for Unapproved Drug Claims

    James G. Cole, Inc. is recalling all ASN brand products nationwide because they are misbranded, adulterated, and unapproved new drugs.

    Product
    ALL ASN products: The ASN products are in capsule or powdered form and bear the ASN label. *********the List of ASN products***************************** AFINITY WHEY PROTEIN; DHEA; HUMAGRO Homeopathic Growth Hormone 4c; PHYTOBOL; TESTRX; TRIBESTRONE II;
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2944-2015·2015-08-19

    Pride of Africa Enriched Farina Recalled for Undeclared Wheat Allergen

    Raymond-Hadley Corp. is recalling Pride of Africa Enriched Farina because the label failed to declare the presence of wheat.

    Product
    Pride of Africa brand Enriched Farina, Net Weight 5 lb. (2.27 kg), UPC 016712016840 --- Product of The Raymond-Hadley Corp. Spencer, NY 14883 --- Product is packaged in a clear plastic pouch with green, brown and white artwork.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·F-2945-2015·2015-08-19

    Lee Egg Rolls Recalled for Undeclared Monosodium Glutamate

    LV Foods is recalling Lee Egg Rolls Vegetables and Textured Vegetable Protein due to undeclared monosodium glutamate (MSG). The product was distributed in California.

    Product
    Lee Egg Rolls Vegetables and Textured Vegetable Protein, Net Wt. 15lbs. 0 oz., Lee Egg Rolls Jacinto City, Texas 77029
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2379-2015·2015-08-19

    Boston Scientific Recalls AngioJet Thrombectomy Sets Due to Incorrect Expiry Date

    Boston Scientific is recalling 9 AngioJet SOLENT Dista Thrombectomy Sets because they were labeled with an incorrect use-by date of December 2015 instead of November 2015.

    Product
    AngioJet SOLENT Dista Thrombectomy Set: UPN 111303-001, Catalog No. 111303, Sterilized Using Ethylene Oxide. For breaking apart and removing thrombus from vascular system, used with the AngioJet Ultra System in breaking apart and r
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2380-2015·2015-08-19

    Boston Scientific Recalls AngioJet AVX Thrombectomy Sets Due to Incorrect Expiry Date

    Boston Scientific is recalling nine AngioJet AVX Thrombectomy Sets because they were labeled with an incorrect use-by date of December 2015 instead of November 2015.

    Product
    AngioJet AVX Thrombectomy Set: UPN 105039-001, Catalog No.105039, Sterilized Using Ethylene Oxide. For breaking apart and removing thrombus from vascular system, used with the AngioJet Ultra System in breaking apart and removing th
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2352-2015·2015-08-19

    Merit Medical Recalls ReSolve Locking Drainage Catheters Due to Labeling Discrepancy

    Merit Medical Systems is voluntarily recalling 950 ReSolve Locking Drainage Catheters because the unit labeling may not match the actual device in the package.

    Product
    ReSolve Locking Drainage Catheters The ReSolve Locking Catheters are intended for percutaneous drainage of fluids from body cavities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2378-2015·2015-08-19

    Boston Scientific Recalls AngioJet Thrombectomy Sets Due to Incorrect Expiry Dates

    Boston Scientific is recalling 9 AngioJet SOLENT Omni Thrombectomy Sets because they were labeled with an incorrect use-by date of December 2015 instead of November 2015.

    Product
    AngioJet SOLENT Omni Thrombectomy Set: UPN 109681-004 & 109681-001, Catalog No 109681, Sterilized. For breaking apart and removing thrombus from vascular system, used with the AngioJet Ultra System in breaking apart and removing t
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2363-2015·2015-08-19

    Stryker Recalls Mispackaged Orthopedic Shoulder Trial Instruments

    Stryker is recalling 21 units of a shoulder trial instrument because the package contained the wrong part number.

    Product
    ReUnion TSA Shoulder System, Standard SR Humeral Head Trial, 48X18, Catalog number 5901-S-4818. Orthopedic manual surgical instrument. Howmedica Osteonics Corp. A Subsidiary of Stryker Corp. Stryker France Non-sterile Made in Cork Ireland
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2360-2015·2015-08-19

    Stryker Recalls Mislabelled Triathlon Tibial Inserts for Knee Replacement

    Stryker Howmedica Osteonics is recalling 26 Triathlon tibial inserts because one unit was found in a package labeled for a different catalog number.

    Product
    Triathlon PS X3 Tibial Insert; No. 3 Triathlon TS Plus Tibial Insert X3 Poly 19 mm Product Usage: The Triathlon PS X3 (posterior stabilized), cat no 5532-G-xxx and X3 TS (total stabilizing) Plus, cat. no. 5537-G-XXX, Tibial Inserts are used in TKA surgeries. During surgery, t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2375-2015·2015-08-19

    Advanced Sterilization Products Recalls STERRAD 100NX Wall Charts for Incorrect Instructions

    Advanced Sterilization Products is recalling 1,465 STERRAD 100NX wall charts because they contain incorrect instructions regarding instrument tray wrapping.

    Product
    Wall Chart for STERRAD 100NX System, P/N 10104. The STERRAD 100NX Sterilizer is designed for sterilization of both metal and nonmetal medical devices at low temperatures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2364-2015·2015-08-19

    Cadence Recalls Perfectum Tuberculin Glass Syringes Due to Misaligned Marks

    Cadence Inc. is recalling 766 non-sterile Perfectum Tuberculin Glass Syringes because graduation marks are not centered with numeric position marks.

    Product
    Perfectum Tuberculin Glass Syringe, Non sterile Catalog numbers 5202, 5205, 5212
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2351-2015·2015-08-19

    Remel Recalls PathoDx Strep B Grouping Latex Reagent

    Remel Inc is recalling PathoDx Strep B Grouping Latex because a reagent may cause weak reactions, potentially leading to failure to identify target species.

    Product
    PathoDx Strep B Grouping Latex, REF 62031, 3 ml packaged in plastic dropper bottle with a pink cap. Latex reagent for streptococcal group B; Identify beta-hemolytic streptococci of Lancefield Groups A, B, C, F and G from primary culture plates.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2953-2015·2015-08-19

    Chemi-source Recalls DHEA 25mg Capsules for Labeling Inaccuracy

    Chemi-source, Inc. is recalling DHEA 25mg capsules because they may contain more DHEA than the label claims.

    Product
    DHEA 25mg, 60 count, sku: #6-09492-41001-6, and 90 count, sku: #6-09492-41002-3; 12 bottles/case.
    Category
    Drug
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2377-2015·2015-08-19

    Boston Scientific Recalls AngioJet Spiroflex Thrombectomy Sets Due to Incorrect Expiry Date

    Boston Scientific is recalling nine AngioJet Spiroflex Thrombectomy Sets because they were labeled with an incorrect use-by date of December 2015 instead of November 2015.

    Product
    AngioJet Spiroflex Thrombectomy Set: Peripheral - UPN 106553-004, Catalog No.106553, Sterilized Using Ethylene Oxide. For breaking apart and removing thrombus from vascular system, used with the AngioJet Ultra System in breaking ap
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Food)·F-2941-2015·2015-08-19

    Janka Apricot Pierogi Recalled for Missing Yellow #5 Labeling

    Krusinskis Finest Meat Products is recalling Janka Fully Cooked Apricot Pierogi because Yellow #5 was not listed on the label.

    Product
    Janka Fully Cooked Apricot Pierogi Ingredients: DOUGH: Blended Flour (Wheat Flour, Malted Barley Flour, Niacin, Iron, Potassium Bromate, Thiamine Mononitrate, Riboflavin), Water, Whole Milk, Eggs, Dried Potatoes (Color and Flavor Protected with Sodium Bisulfate, Citric Acid and B
    Category
    Food
    Distribution
    1 state
  • LowFDA (Food)·F-2951-2015·2015-08-19

    Mason Vitamins Recalls Mislabeled Coenzyme Q-10 50 mg Softgels

    Mason Vitamins, Inc. is recalling 13,027 bottles of Coenzyme Q-10 50 mg softgels because some bottles were mislabeled with the wrong dosage.

    Product
    Coenzyme Q-10 50 mg label reads in part, "***Major***CO Q-10 50 MG***For healthy HEART & IMMUNE function***Promotes ENERGY in all Body Cells***Dietary Supplement 30 SOFTGELS***."
    Category
    Food
    Distribution
    31 states
  • HighFDA (Food)·F-2932-215·2015-08-12

    Nabisco Fig Newtons Recalled for Undeclared Milk Allergen

    Mondelez International is recalling Nabisco Fig Newtons because the outer carton fails to declare milk, a major allergen, while the inner packaging does.

    Product
    Outer carton : Nabisco Newtons Fig 24-2 OZ (56 g) Packs Net Wt 3 lbs Mondelez International Mondelez Global LLC East Hanover, NJ 07936 USA Made in Mexico case UPC 0 44000 03445 0 Inner Pouch: Nabisco Newtons Fig Net Wt 2 oz (56 g) Mondelez Global LLC, East Hanover, NJ
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2933-2015·2015-08-12

    Cowden's Lycoming Bakery Pizza Shells Recalled for Undeclared Milk Allergen

    Cowden's Lycoming Bakery is recalling 123 units of 2-pack pizza shells because they contain whey, a milk allergen, that was not listed on the label.

    Product
    2 fully baked pizza shells packed in plastic bag with labeling reading: Cowden's Lycoming Bakery 220 Curtain St, South Williamsport, PA; 2 Pizza Shells Net Wt. 20 oz. Ingredients: ***Flour (Hard Spring wheat flour), water, shortening (partially hydrogenated soybean and co
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2346-2015·2015-08-12

    Atrium 36Fr Right Angled Firm PVC Thoracic Catheter Recall

    Atrium Medical Corporation is recalling 620 units of 36Fr Right Angled Firm PVC Thoracic Catheters due to incorrect labeling on inner pouches.

    Product
    Atrium 36Fr Right Angled Firm PVC Thoracic Catheter, (Pkg of 10) Part Number: 15236
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Food)·F-2926-2015·2015-08-12

    La Jalpita Vanilla Bolis Recalled for Undeclared Yellow No. 6

    Paleteria La Jalpita is recalling 1,350 units of Vanilla bolis (tube) sold in Oregon and Washington due to undeclared Yellow No. 6.

    Product
    Vanilla bolis (tube), La Jalpita brand, 3.5 Fl oz., No UPC
    Category
    Food
    Distribution
    2 states